Trans fat

Last updated
Margarine, which can contain trans fat. Margaryn 022.jpg
Margarine, which can contain trans fat.

Trans fat, also called trans-unsaturated fatty acids, or trans fatty acids, is a type of unsaturated fat that occurs in foods. Small amounts of trans fats occur naturally, but large amounts are found in some processed foods. Since consumption of trans fats is unhealthy, [lower-alpha 1] artificial trans fats are highly regulated or banned in many nations. However, they are still widely consumed in developing nations, resulting in hundreds of thousands of deaths each year. [8] The World Health Organization (WHO) had set a goal to make the world free from industrially produced trans fat by the end of 2023. [9] The goal was not met, and the WHO announced another goal "for accelerated action till 2025 to complete this effort" along with associated support on 1 February 2024. [10]

Contents

Occurrence

Some trans fats arise naturally, and some are the result of human actions.

Naturally-occurring trans fats

Vaccenic acid, a naturally occurring trans fatty acid, comprises 0.4-4% of the total fatty acid content in dairy milk. Trans-vaccenic acid.svg
Vaccenic acid, a naturally occurring trans fatty acid, comprises 0.4–4% of the total fatty acid content in dairy milk.

Trans fats occur in meat and dairy products from ruminants. For example, butter contains about 3% trans fat by weight. [11] These naturally occurring trans fats include conjugated linoleic acid (CLA) and vaccenic acid. They arise from the action of bacteria in the rumen. Polyunsaturated fats are toxic to the rumen-based bacteria, which detoxify the fats by changing some cis-double bonds to trans-double bonds. In contrast to industrially produced trans fats, this bacterial process produces only a few specific isomers. As industrial sources of trans fats are eliminated, increased attention focuses on ruminant derived trans fats. [12]

The trans fatty acid vaccenic acid has health benefits. [13] [14] [15] [16] Small amounts occur in meat and milk fat. [17]

Hydrogenation

Trans fat can be an unintentional byproduct of the industrial processing of oils. Unlike naturally derived trans fats, the trans fats that result from hydrogenation consist of many isomers. In food production, liquid cis-unsaturated fats such as vegetable oils are hydrogenated to produce more saturated fats, which have desirable properties:

However, an isomerization side reaction during fat hydrogenation can convert remaining unsaturated fats to the thermodynamically-favored trans isomer.

The desirable (left) and undesirable pathways for partial hydrogenation of an unsaturated fat. FatHydrogenation.svg
The desirable (left) and undesirable pathways for partial hydrogenation of an unsaturated fat.

A number of old and new ingredients are available to replace partially-hydrogenated oil containing significant levels of trans fat. These include partially-hydrogenated oil made with improved processes, plant oils rich in monounsaturated fats and saturated fats, and a mix of fats combined with interesterification. [18] The technology has improved such that a 2021 review indicates that trans fat from hydrogenated fats is no longer a problem in modern countries. [12]

Thermal isomerization

When heated (cooked), some unsaturated fats change from their normal geometry to trans. The rate of isomerization is accelerated by free radicals. [19] [20] [21]

History

Cover of original Crisco cookbook, 1912 Crisco Cookbook 1912.jpg
Cover of original Crisco cookbook, 1912

The German chemist Wilhelm Normann showed that liquid oils could be hydrogenated. He patented the process in 1902. [22] [23] [24] During the years 1905–1910, Normann built a fat-hardening facility in the Herford company. At the same time, the invention was extended to a large-scale plant in Warrington, England, at Joseph Crosfield & Sons, Limited. It took only two years until the hardened fat could be successfully produced in the plant in Warrington, commencing production in the autumn of 1909. The initial year's production totalled nearly 3,000 tonnes. [25] In 1909, Procter & Gamble acquired the United States rights to the Normann patent; [26] in 1911, they began marketing the first hydrogenated shortening, Crisco (composed largely of partially hydrogenated cottonseed oil). Further success came from the marketing technique of giving away free cookbooks in which every recipe called for Crisco.

Normann's hydrogenation process made it possible to stabilize affordable whale oil or fish oil for human consumption, a practice kept secret to avoid consumer distaste. [25]

Before 1910, dietary fats in industrialized nations consisted mostly of butterfat, beef tallow, and lard. During Napoleon's reign in France in the early 19th century, a type of margarine was invented to feed troops using tallow and buttermilk. Soybeans began to be imported into the U.S. as a source of protein in the early 20th century, resulting in an abundance of soybean oil as a by-product that could be turned into a solid fat, thereby addressing a shortage of butterfat. Furthermore, with the advent of refrigeration, margarines based on hydrogenated fats presented the advantage that, unlike butter, they could be taken out of a refrigerator and immediately spread on bread. Some minor changes to the chemical composition of hydrogenated fats yielded superior baking properties compared to lard. As a result of these factors, margarine made from partially hydrogenated soybean oil began to replace butterfat. Partially hydrogenated fat such as Crisco and Spry, sold in England, began to replace butter and lard in baking bread, pies, cookies, and cakes in 1920. [27]

Production of partially hydrogenated fats increased steadily in the 20th century as processed vegetable fats replaced animal fats in the U.S. and other Western countries. At first, the argument was a financial one due to the lower costs of margarines and shortenings compared to lard and butter, particularly for restaurants and manufacturers. However, during the 1980s regulators, physicians, nutritionists, popular health media, educational curricula and cookbooks began to promote diets low in saturated fats for health reasons. Advocacy groups in the U.S. responded by demanding the replacement of saturated animal and tropical fats with vegetable alternatives. The Center for Science in the Public Interest (CSPI) campaigned vigorously against the use of saturated fats by corporations, including fast-food restaurants, endorsing trans fats as a healthier alternative. The National Heart Savers Association took out full page ads in major newspapers, attacking the use of beef tallow in McDonald's French fries. They urged multinational fast-food restaurants and food manufacturers to switch to vegetable oils, and almost all targeted firms responded by replacing saturated fats with trans fats. [28] [29] [30]

Although this shift to trans fats was rooted in health concerns, there were suggestions in the scientific literature as early as 1956 that trans fats themselves could actually be a cause of a large increase in coronary artery disease. [31] Studies in the early 1990s brought renewed scrutiny and confirmation of the negative health impact of trans fats. In 1994, it was estimated that trans fats caused at least 20,000 deaths annually in the U.S. from heart disease. [32] In the 1990s, activists such as CSPI that had promoted trans fat safety began arguing that trans fats should be disclosed on product labels and menus. [33] Several lawsuits were launched against high-visibility restaurants and food manufacturers with the objective of supporting a broader phase-out of trans fats. [34] [35]

Mandatory food labeling was introduced in several countries [36] and Denmark was first to mandate limits on industrially-produced trans fats in 2004. [37] In January 2007, faced with the prospect of an outright ban on the sale of their product, Crisco was reformulated to meet the U.S. Food and Drug Administration (FDA) definition of "zero grams trans fats per serving" (that is less than one gram per tablespoon, or up to 7% by weight; or less than 0.5 grams per serving size) [38] [39] [40] [41] by boosting the saturation and then diluting the resulting solid fat with unsaturated vegetable oils. Noting that elimination of industrially produced trans fat is feasible and achievable, the World Health Organization (WHO) has set a goal to make the world free from industrially produced trans fat by the end of 2023. By the end of 2021, the WHO announced that 40 countries had implemented industrial trans fat elimination policies that "are protecting 1.4 billion people from this deadly food compound" but that 10 of the 15 countries suffering the highest health impacts from trans fats had not yet adopted a policy. [9]

Structure

A fatty acid is characterized as either saturated or unsaturated based on the respective absence or presence of C=C double bonds in its backbone. If the molecule contains no double C=C bonds, it is said to be saturated; otherwise, it is unsaturated to some degree. [42] [43]

The C=C double bond is rotationally rigid. If the hydrogen bonded to each of the carbons in this double bond are on the same side, this is called cis, and leads to a bent molecular chain. If the two hydrogens are on opposite sides, this is called trans, and leads to a straight chain.

Trans unsaturated (Elaidic acid)Cis unsaturated (Oleic acid)Saturated (Stearic acid)
Elaidic acid is the main trans unsaturated fatty acid often found in partially hydrogenated vegetable oils. [44] Oleic acid is a cis unsaturated fatty acid making up 55–80% of olive oil. [45] Stearic acid is a saturated fatty acid found in animal fats and is the intended product in full hydrogenation. Stearic acid is neither unsaturated nor trans because it has no carbon-carbon double bonds.
Elaidic-acid-3D-vdW.png
Oleic-acid-3D-vdW.png
Stearic-acid-3D-balls.png
Elaidic acid v2.svg
Oleic-acid-skeletal.svg
Stearic acid.svg
These fatty acids are geometric isomers (structurally identical except for the arrangement of the double bond).This fatty acid contains no carbon-carbon double bonds and is not isomeric with the prior two.

Because trans fats are more linear, they crystallize more easily, allowing them to be solid (rather than liquid) at room temperatures. This has several processing and storage advantages.

In nature, unsaturated fatty acids generally have cis configurations as opposed to trans configurations. [46] Saturated fatty acids (those without any carbon-carbon double bonds) are abundant (see tallow), but they also can be generated from unsaturated fats by the process of fat hydrogenation. In the course of hydrogenation, some cis double bonds convert into trans double bonds. Chemists call this conversion an isomerization reaction. [20] [21] [47]

Wilhelm Normann patented the hydrogenation of liquid oils in 1902 Wilhelm Normann.jpg
Wilhelm Normann patented the hydrogenation of liquid oils in 1902

Hydrogenation of an unsaturated fatty acid is intended to convert unsaturated fatty acids (and unsaturated fats) to saturated derivatives. The hydrogenation process however can cause cis C=C bonds to become trans. Typical commercial hydrogenation is partial to obtain a malleable mixture of fats that is solid at room temperature, but melts during baking, or consumption.

The same molecule, containing the same number of atoms, with a double bond in the same location, can be either a trans or a cis fatty acid depending on the configuration of the double bond. For example, oleic acid and elaidic acid are both unsaturated fatty acids with the chemical formula C9H17C9H17O2. [48] They both have a double bond located midway along the carbon chain. It is the configuration of this bond that sets them apart. The configuration has implications for the physical-chemical properties of the molecule. The trans configuration is straighter, while the cis configuration is noticeably kinked as can be seen from the three-dimensional representation shown above. Cis- and trans fatty acids (and their derivatives) have distinct chemical (and metabolic) properties, For example, the melting point of elaidic acid is 45  °C higher than that of oleic acid. [48] This notably means that it is a solid at human body temperatures.

In the sense of food production, however, the goal is not necessarily to simply change the configuration of double bonds while maintaining the same ratios of hydrogen to carbon; rather, the goal is to decrease the number of double bonds (when a fatty acid molecule contains more than one double bond it is classified as "polyunsaturated") by increasing the amount of hydrogen (and, thus, single bonds) in the fatty acid. This subsequent lesser degree of unsaturation (and, simultaneously, greater degree of saturation) thereby changes the consistency of the fatty acid by way of allowing its molecules to more greatly compress and congeal and in turn thereby makes it less prone to rancidity (in which free radicals attack double bonds). In this second sense of the goal being to simply reduce the degree of unsaturation in an unsaturated fatty acid, the production of trans fatty acids is thus an undesirable side effect of partial hydrogenation.

Catalytic partial hydrogenation produces some trans-fats. The standard 140 kPa (20 psi) process of hydrogenation produces a product of about 40% trans fatty acid by weight, compared to about 17% using higher pressures of hydrogen. Blended with unhydrogenated liquid soybean oil, the high-pressure-processed oil produced margarine containing 5 to 6% trans fat. Based on current U.S. labeling requirements (see below), the manufacturer could claim the product was free of trans fat. [49] The level of trans fat may also be altered by modification of the temperature and the length of time during hydrogenation.

The trans fat levels can be quantified using various forms of chromatography. [19]

Presence in food

Trans fat contents in various foods, ranked in g per 100 g [50]
Food typeTrans fat content
shortenings10–33
margarine, stick6.2–16.8 [51]
butter2–7
whole milk0.07–0.1
breads/cake products0.1–10
cookies and crackers1–8
tortilla chips5.8 [51]
cake frostings, sweets0.1–7
animal fat0–5 [52]
ground beef1

A type of trans fat occurs naturally in the milk and body fat of ruminants (such as cattle and sheep) at a level of 2–5% of total fat. [52] Natural trans fats, which include conjugated linoleic acid (CLA) and vaccenic acid, originate in the rumen of these animals. CLA has two double bonds, one in the cis configuration and one in trans, which makes it simultaneously a cis- and a trans-fatty acid.

Animal-based fats were once the only trans fats consumed, but by far the largest amount of trans fat consumed today is created by the processed food industry as a side effect of partially hydrogenating unsaturated plant fats (generally vegetable oils). These partially hydrogenated fats have displaced natural solid fats and liquid oils in many areas, the most notable ones being in the fast food, snack food, fried food, and baked goods industries. [53]

Partially hydrogenated oils have been used in food for many reasons. Hydrogenation increases product shelf life and decreases refrigeration requirements. Many baked foods require semi-solid fats to suspend solids at room temperature; partially hydrogenated oils have the right consistency to replace animal fats such as butter and lard at lower cost. They are also an inexpensive alternative to other semi-solid oils such as palm oil.[ citation needed ]

Reaction scheme: Trans fat is created as a side effect of partially catalytic hydrogenation of unsaturated plant fats (generally vegetable oils) with cis carbon-carbon double bonds. Triglyceride Hydrogenation&Isomerization V.1.png
Reaction scheme: Trans fat is created as a side effect of partially catalytic hydrogenation of unsaturated plant fats (generally vegetable oils) with cis carbon-carbon double bonds.

Up to 45% of the total fat in those foods containing human-made trans fats formed by partially hydrogenating plant fats may be trans fat. [52] Baking shortenings, unless reformulated, contain around 30% trans fats compared to their total fats. High-fat dairy products such as butter contain about 4%. Margarines not reformulated to reduce trans fats may contain up to 15% trans fat by weight, [54] but some reformulated ones are less than 1% trans fat.

It has been established that trans fats in human breast milk fluctuate with maternal consumption of trans fat, and that the amount of trans fats in the bloodstream of breastfed infants fluctuates with the amounts found in their milk. In 1999, reported percentages of trans fats (compared to total fats) in human milk ranged from 1% in Spain, 2% in France, 4% in Germany, and 7% in Canada and the U.S. [55]

Trans fats are used in shortenings for deep-frying in restaurants, as they can be used for longer than most conventional oils before becoming rancid. In the early 21st century, non-hydrogenated vegetable oils that have lifespans exceeding that of the frying shortenings became available. [56] As fast-food chains routinely use different fats in different locations, trans fat levels in fast food can have large variations. For example, an analysis of samples of McDonald's French fries collected in 2004 and 2005 found that fries served in New York City contained twice as much trans fat as in Hungary, and 28 times as much as in Denmark, where trans fats are restricted. At KFC, the pattern was reversed, with Hungary's product containing twice the trans fat of the New York product. Even within the U.S. there was variation, with fries in New York containing 30% more trans fat than those from Atlanta. [57]

Nutritional guidelines

The National Academy of Sciences (NAS) advises the U.S. and Canadian governments on nutritional science for use in public policy and product labeling programs. Their 2002 Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids [58] contains their findings and recommendations regarding consumption of trans fat (summary).

Their recommendations are based on two key facts. First, "trans fatty acids are not essential and provide no known benefit to human health", [59] whether of animal or plant origin. [60] Second, while both saturated and trans fats increase levels of low-density lipoprotein (LDL), trans fats also lower levels of high-density lipoprotein (HDL), [61] thus increasing the risk of coronary artery disease. The NAS is concerned "that dietary trans fatty acids are more deleterious with respect to coronary artery disease than saturated fatty acids". [61] This analysis is supported by a 2006 New England Journal of Medicine scientific review that states "from a nutritional standpoint, the consumption of trans fatty acids results in considerable potential harm but no apparent benefit." [62]

Because of these facts and concerns, the NAS has concluded there is no safe level of trans fat consumption. There is no adequate level, recommended daily amount or tolerable upper limit for trans fats. This is because any incremental increase in trans fat intake increases the risk of coronary artery disease. [61]

Despite this concern, the NAS dietary recommendations have not included eliminating trans fat from the diet. This is because trans fat is naturally present in many animal foods in trace quantities, and thus its removal from ordinary diets might introduce undesirable side effects and nutritional imbalances if proper nutritional planning is not undertaken. The NAS has, thus, "recommended that trans fatty acid consumption be as low as possible while consuming a nutritionally adequate diet". [63] Like the NAS, the World Health Organization has tried to balance public health goals with a practical level of trans fat consumption, recommending in 2003 that trans fats be limited to less than 1% of overall energy intake. [52]

The US National Dairy Council has asserted that the trans fats present in foods of animal origin are of a different type than those in partially hydrogenated oils, and do not appear to exhibit the same negative effects. [64] A scientific review agrees with the conclusion (stating that "the sum of the current evidence suggests that the Public health implications of consuming trans fats from ruminant products are relatively limited") but cautions that this may be due to the low consumption of trans fats from animal sources compared to artificial ones. [62]

A meta-analysis showed that all trans fats, regardless of natural or artificial origin equally raise LDL and lower HDL levels. [65] Other studies though have shown different results when it comes to animal based trans fats like conjugated linoleic acid (CLA). Although CLA is known for its anticancer properties, researchers have also found that the cis-9, trans-11 form of CLA can reduce the risk for cardiovascular disease and help fight inflammation. [66] [67]

Health risks

Partially hydrogenated vegetable oils were an increasingly significant part of the human diet for about 100 years, especially after 1950 as processed food rose in popularity. [68] The deleterious effects of trans fat consumption are scientifically accepted.

Intake of dietary trans fat disrupts the body's ability to metabolize essential fatty acids (EFAs, including Omega-3) leading to changes in the phospholipid fatty acid composition of the arterial walls, thereby raising risk of coronary artery disease. [69]

While the mechanisms through which trans fatty acids contribute to coronary artery disease are understood, the mechanism for their effects on diabetes is still under investigation. They may impair the metabolism of long-chain polyunsaturated fatty acids (LCPUFAs), [70] but maternal pregnancy trans fatty acid intake has been inversely associated with LCPUFAs levels in infants at birth thought to underlie the positive association between breastfeeding and intelligence. [71]

Consumption of industrial trans fat in the form of partially hydrogenated oil causes many health problems. [72] They were abundant in fast food restaurants. [68] They are consumed in greater quantities by people who lack access to a diet consisting of fewer partially-hydrogenated fats, or who often consume fast food. A diet high in trans fats can contribute to obesity, high blood pressure, and higher risk for heart disease. Trans fat is also implicated in Type 2 diabetes. [73]

Coronary artery disease

The most important health risk identified for trans fat consumption is an elevated risk of coronary artery disease (CAD). [74] A 1994 study estimated that over 30,000 cardiac deaths per year in the U.S. are attributable to the consumption of trans fats. [32] By 2006 upper estimates of 100,000 deaths were suggested. [75] A comprehensive review of studies of trans fats published in 2006 in the New England Journal of Medicine reports a strong and reliable connection between trans fat consumption and CAD, concluding that "On a per-calorie basis, trans fats appear to increase the risk of CAD more than any other macronutrient, conferring a substantially increased risk at low levels of consumption (1 to 3% of total energy intake)". [62]

The major evidence for the effect of trans fat on CAD comes from the Nurses' Health Study – a cohort study that has been following 120,000 female nurses since its inception in 1976. In this study, Hu and colleagues analyzed data from 900 coronary events from the study's population during 14 years of followup. He determined that a nurse's CAD risk roughly doubled (relative risk of 1.93, CI: 1.43 to 2.61) for each 2% increase in trans fat calories consumed (instead of carbohydrate calories). By contrast, for each 5% increase in saturated fat calories (instead of carbohydrate calories) there was a 17% increase in risk (relative risk of 1.17, CI: 0.97 to 1.41). "The replacement of saturated fat or trans unsaturated fat by cis (unhydrogenated) unsaturated fats was associated with larger reductions in risk than an isocaloric replacement by carbohydrates." [76] Hu also reports on the benefits of reducing trans fat consumption. Replacing 2% of food energy from trans fat with non-trans unsaturated fats more than halves the risk of CAD (53%). By comparison, replacing a larger 5% of food energy from saturated fat with non-trans unsaturated fats reduces the risk of CAD by 43%. [76]

Another study considered deaths due to CAD, with consumption of trans fats being linked to an increase in mortality, and consumption of polyunsaturated fats being linked to a decrease in mortality. [74] [77]

There are two accepted tests that measure an individual's risk for coronary artery disease, both blood tests. The first considers ratios of two types of cholesterol, the other the amount of a cell-signalling cytokine called C-reactive protein. The ratio test is more accepted, while the cytokine test may be more powerful but is still being studied. [74] The effect of trans fat consumption has been documented on each as follows:

Other health risks

Scientific studies have examined other negative effects of industrial trans fat beyond cardiovascular disease, with the next most studied area being type-2 diabetes.

Public response and regulation

International

The international trade in food is standardized in the Codex Alimentarius. Hydrogenated oils and fats come under the scope of Codex Stan 19. [105] Non-dairy fat spreads are covered by Codex Stan 256-2007. [106] In the Codex Alimentarius, trans fat to be labelled as such is defined as the geometrical isomers of monounsaturated and polyunsaturated fatty acids having non-conjugated [interrupted by at least one methylene group (−CH2−)] carbon-carbon double bonds in the trans configuration. This definition excludes specifically the trans fats (vaccenic acid and conjugated linoleic acid) that are present especially in human milk, dairy products, and beef.[ citation needed ]

In 2018 the World Health Organization launched a plan to eliminate trans fat from the global food supply. They estimate that trans fat leads to more than 500,000 deaths from cardiovascular disease yearly. [107]

Argentina

Trans fat content labeling is required starting in August 2006. [108] Since 2010, vegetable oils and fats sold to consumers directly must contain only 2% of trans fat over total fat, and other food must contain less than 5% of their total fat. [109] Starting on 10 December 2014, Argentina has on effect a total ban on food with trans fat, a regulation the government estimated could save them more than US$100 million a year on healthcare. [110]

Australia

The former federal assistant health minister, Christopher Pyne, asked fast food outlets to reduce their trans fat use. A draft plan was proposed, with a September 2007 timetable, to reduce reliance on trans fats and saturated fats. [111]

As of 2018, Australia's food labeling laws do not require trans fats to be shown separately from the total fat content. However, margarine in Australia has been mostly free of trans fat since 1996. [112]

Austria

Trans fat content is limited to 4% of total fat, or 2% on products that contain more than 20% fat. [113]

Belgium

The Conseil Supérieur de la Santé published in 2012 a science-policy advisory report on industrially produced trans fatty acids that focuses on the general population. Its recommendation to the legislature was to prohibit more than 2 g of trans fatty acids per 100 g of fat in food products. [114]

Brazil

Resolution 360, dated December 23, 2003, by the Brazilian ministry of health required the amount of trans fat to be specified in labels of food products. On 31 July 2006, such labeling of trans fat contents became mandatory. In 2019 Anvisa published a new legislation to reduce the total amount of trans fat in any industrialized food sold in Brazil to a maximum of 2% by the end of 2023. [115]

Since January 1, 2023, the use, production and import of hydrogenated vegetable oils in food for consumption has been completely banned by Anvisa. [116]

Canada

In a process that began in 2004, Health Canada finally banned partially hydrogenated oils (PHOs), the primary source of industrially produced trans fats in foods, in September 2018.

On 15 September 2017, Health Canada announced that trans fat would be completely banned effective on 15 September 2018. [117] The ban came into effect in September 2018, banning partially hydrogenated oils (the largest source of industrially produced trans fats in foods). It is now illegal for manufacturers to add partially hydrogenated oils to foods sold in or imported into Canada. [118]

Public perception

A cross-sectional study was conducted in Regina, Saskatchewan in February 2009 at 3 different grocery stores located in 3 different regions that had the same median income before taxes of around $30,000. Of the 211 respondents to the study, most were women who purchased most of the food for their household. When asked how they decide what food to buy, the most important factors were price, nutritional value, and need. When looking at the nutritional facts, however, they indicated that they looked at the ingredients, and neglected to pay attention to the amount of trans fat. This means that trans fat is not on their minds unless they are specifically told of it. When asked if they ever heard about trans fat, 98% said, "Yes." However, only 27% said that it was unhealthy. Also, 79% said that they only knew a little about trans fats, and could have been more educated.

Respondents aged 41–60 were more likely to view trans fat as a major health concern, compared to ages 18–40. When asked if they would stop buying their favorite snacks if they knew it contained trans fat, most said they would continue purchasing it, especially the younger respondents. Also, of the respondents that called trans fat a major concern, 56% of them still would not change their diet to non-trans fat snacks. This is because taste and food gratification take precedence over perceived risk to health. "The consumption of trans fats and the associated increased risk of CHD is a public health concern regardless of age and socioeconomic status". [119]

Denmark

Denmark became the first country to introduce laws strictly regulating the sale of many foods containing trans fats [120] in March 2003, a move that effectively bans partially hydrogenated oils. The limit is 2% of fats and oils destined for human consumption. This restriction is on the ingredients rather than the final products. This regulatory approach has made Denmark the first country in which it is possible to eat "far less" than 1 g of industrially produced trans fats daily, even with a diet including prepared foods. [121] It is hypothesized that the Danish government's efforts to decrease trans fat intake from 6 g to 1 g per day over 20 years is related to a 50% decrease in deaths from ischemic heart disease. [122]

European Union

In 2004, the European Food Safety Authority produced a scientific opinion on trans fatty acids, surmising that "higher intakes of TFA may increase risk for coronary heart disease". [123]

From 2 April 2021 foods in the EU intended for consumers are required to contain less than 2g of industrial trans fat per 100g of fat. [124]

Greece

Law in Greece limits content of trans fats sold in school canteens to 0.1% (Ministerial Decision Υ1γ/ΓΠ/οικ 81025/ΦΕΚ 2135/τ.Β'/29-08-2013 as modified by Ministerial Decision Υ1γ/ Γ.Π/οικ 96605/ΦΕΚ 2800 τ.Β/4-11-201). [125]

Iceland

Total trans fat content was limited in 2010 to 2% of total fat content. [126] [127]

Israel

Since 2014, it is obligatory to mark food products with more than 2% (by weight) fat. The nutritional facts must contain the amount of trans fats. [128]

Pakistan

Ministry of National Health Services Regulations and Coordination, Government of Pakistan with the support of WHO has taken the initiative to eliminate trans fat from food chain in Pakistan. Vanaspati Ghee (partially hydrogenated fat) and margarine have been identified as major dietary vectors for trans fat. PSQCA (Pakistan Standard and Quality Control Authority) has set the deadline for the reduction of trans fat level as per recommendations of WHO by June 2023.

Philippines

The Department of Health has reminded food companies to reformulate and remove industrially produced trans fatty acids (TFA) from their products by June 18, 2023. It said that non-communicable diseases (NCDs) such as cardiovascular disease have been one of the leading causes of death in the country. All product formulations and labels of prepackaged processed food with industrially-produced TFA must comply with the guidelines stated in the DOH Administrative Order No. 2021-0039 and the FDA Circular No. 2021- 0028. Violation of any of the provisions of the administrative order and the FDA circular would be grounds for the disapproval, suspension, or cancellation of the certificate of product registration of concerned food manufacturers. [129]

Saudi Arabia

The Saudi Food and Drug Authority (SFDA) requires importers and manufacturers to write trans fats amounts in the nutritional facts labels of food products according to the requirements of Saudi Standard Specifications/Gulf Specifications. [130] Starting in 2020, Saudi Minister of Health announced the ban of trans fat in all food products due to their health risks. [131]

Singapore

The Ministry of Health announced on 6 March 2019 that partially-hydrogenated oils (PHOs) will be banned. [132] A target is set to ban PHOs by June 2021, aiming to encourage healthy eating habits. [133]

Sweden

The parliament gave the government a mandate in 2011 to submit without delay a law prohibiting the use of industrially produced trans fats in foods, as of 2017 the law has not yet been implemented. [134] [135]

Switzerland

Switzerland followed Denmark's trans fats ban, and implemented its own starting in April 2008. [136]

United Kingdom

In October 2005, the Food Standards Agency (FSA) asked for better labelling in the UK. [137] In the edition of 29 July 2006 of the British Medical Journal , an editorial also called for better labelling. [138] In January 2007, the British Retail Consortium announced that major UK retailers, including Asda, Boots, Co-op Food, Iceland, Marks and Spencer, Sainsbury's, Tesco and Waitrose [139] intended to cease adding trans fatty acids to their own products by the end of 2007. [140]

Sainsbury's became the first UK major retailer to ban all trans fat from all their own store brand foods.

On 13 December 2007, the Food Standards Agency issued news releases stating that voluntary measures to reduce trans fats in food had already resulted in safe levels of consumer intake. [141] [142]

On 15 April 2010, a British Medical Journal editorial called for trans fats to be "virtually eliminated in the United Kingdom by next year". [143]

The June 2010 National Institute for Health and Clinical Excellence (NICE) report Prevention of cardiovascular disease declared that 40,000 cardiovascular disease deaths in 2006 were "mostly preventable". [144] To achieve this, NICE offered 24 recommendations including product labelling, public education, protecting under–16s from marketing of unhealthy foods, promoting exercise and physically active travel, and even reforming the Common Agricultural Policy to reduce production of unhealthy foods. Fast-food outlets were mentioned as a risk factor, with (in 2007) 170 g of McDonald's fries and 160 g nuggets containing 6 to 8 g of trans fats, conferring a substantially increased risk of coronary artery disease death. [145] NICE made three specific recommendation for diet: (1) reduction of dietary salt to 3 g per day by 2025; (2) halving consumption of saturated fats; and (3) eliminating the use of industrially produced trans fatty acids in food. However, the recommendations were greeted unhappily by the food industry, which stated that it was already voluntarily dropping the trans fat levels to below the WHO recommendations of a maximum of 2%.[ citation needed ]

Rejecting an outright ban, the Health Secretary Andrew Lansley launched on 15 March 2012 a voluntary pledge to remove artificial trans fats by the end of the year. Asda, Pizza Hut, Burger King, Tesco, Unilever and United Biscuits are some of 73 businesses who have agreed to do so.[ citation needed ] Lansley and his special Adviser Bill Morgan formerly worked for firms with interests in the food industry and some journalists have alleged that this results in a conflict of interest. [146] Many health professionals are not happy with the voluntary nature of the deal. Simon Capewell, Professor of Clinical Epidemiology at the University of Liverpool, felt that justifying intake on the basis of average figures was unsuitable since some members of the community could considerably exceed this. [147]

United States

Before 1 January 2006, consumers in the U.S. could not always determine the presence, or quantity, of trans fats from partially hydrogenated oils in food products, because this information was not required on the ingredient list before that date. In 2010, according to the FDA, the average American consumed 5.8 grams of trans fat per day (2.6% of energy intake). [148] Monoglycerides and diglycerides are not considered fats by the FDA, despite their nearly equal calorie per weight contribution during ingestion. [149]

On 11 July 2003, the FDA issued a regulation requiring manufacturers to list trans fat on the Nutrition Facts panel of foods and some dietary supplements. [38] [39] The new labeling rule became mandatory across the board on 1 January 2006, even for companies that petitioned for extensions. However, unlike in many other countries, trans fat levels of less than 0.5 grams per serving can be listed as 0 grams trans fat on the food label. [150] According to a study published in the Journal of Public Policy & Marketing, without an interpretive footnote or further information on recommended daily value, many consumers do not know how to interpret the meaning of trans fat content on the Nutrition Facts panel. Without specific prior knowledge about trans fat and its negative health effects, consumers, including those at risk for heart disease, may misinterpret nutrient information provided on the panel. [40] The FDA did not approve nutrient content claims such as "trans fat free" or "low trans fat", as they could not determine a "recommended daily value". In July 2023, the agency published notice of plans for a consumer study to evaluate the consumer understanding of such claims and perhaps consider regulation allowing their use on packaged foods. [151] However, there is no requirement to list trans fats on institutional food packaging; thus bulk purchasers such as schools, hospitals, jails and cafeterias are unable to evaluate the trans fat content of commercial food items. [152]

An example of trans fat provided by the FDA. Avoiding Trans Fat (18520422550).jpg
An example of trans fat provided by the FDA.

Critics of the plan, including FDA advisor Dr. Carlos Camargo, have expressed concern that the 0.5 gram per serving threshold is too high to refer to a food as free of trans fat. This is because a person eating many servings of a product, or eating multiple products over the course of the day may still consume a significant amount of trans fat. [41]

The American Medical Association supports any state and federal efforts to ban the use of artificial trans fats in U.S. restaurants and bakeries. [153]

The American Public Health Association adopted a new policy statement regarding trans fats in 2007. These new guidelines, entitled Restricting Trans Fatty Acids in the Food Supply, recommend that the government require nutrition facts labeling of trans fats on all commercial food products. They also urge federal, state, and local governments to ban and monitor use of trans fats in restaurants. Furthermore, the APHA recommends barring the sales and availability of foods containing significant amounts of trans fat in public facilities including universities, prisons, and day care facilities etc. [152]

2015–2019 phaseout

In 2009, at the age of 94, University of Illinois professor Fred Kummerow, a trans fat researcher who had campaigned for decades for a federal ban on the substance, filed a petition with the FDA seeking elimination of artificial trans fats from the U.S. food supply. [154] The FDA did not act on his petition for four years, and in 2013 Kummerow filed a lawsuit against the FDA and the U.S. Department of Health and Human Services, seeking to compel the FDA to respond to his petition and "to ban partially hydrogenated oils unless a complete administrative review finds new evidence for their safety." [154] Kummerow's petition stated that "Artificial trans fat is a poisonous and deleterious substance, and the FDA has acknowledged the danger." [155]

Three months after the suit was filed, on 7 November 2013, the FDA issued a preliminary determination that trans fats are not "generally recognized as safe", which was widely seen as a precursor to reclassifying trans fats as a "food additive," meaning they could not be used in foods without specific regulatory authorization. This would have the effect of virtually eliminating trans fats from the US food supply. [156] [21] [157] The ruling was formally enacted on 16 June 2015, requiring that within three years no food prepared in the U.S. is allowed to include trans fats, unless approved by the FDA. [158] [159] The FDA specifically ruled that trans fat was not generally recognized as safe and "could no longer be added to food after 18 June 2018, unless a manufacturer could present convincing scientific evidence that a particular use was safe." [160] [161] [162] [163] Kummerow stated: "Science won out." [164]

The ban is believed to prevent about 90,000 premature deaths annually. [160] The FDA estimates the ban will cost the food industry $6.2 billion over 20 years as the industry reformulates products and substitutes new ingredients for trans fat. The benefits are estimated at $140 billion over 20 years mainly from lower health care spending. [165]

The FDA agreed in May 2018 to give companies one more year to find other ingredients for enhancing product flavors or greasing industrial baking pans, effectively banning trans fats in the U.S. from May 2019 onwards. Also, while new products can no longer be made with trans fats, foods already on the shelves are given some time to cycle out of the market. [166]

Food industry response

Manufacturer response

Palm oil, a natural oil extracted from the fruit of oil palm trees that is semi-solid at room temperature (15–25 degrees Celsius), can potentially serve as a substitute for partially hydrogenated fats in baking and processed food applications, although there is disagreement about whether replacing partially hydrogenated fats with palm oil confers any health benefits. A 2006 study supported by the National Institutes of Health and the USDA Agricultural Research Service concluded that palm oil is not a safe substitute for partially hydrogenated fats (trans fats) in the food industry, because palm oil results in adverse changes in the blood concentrations of LDL and apolipoprotein B just as trans fat does. [167] [168]

In May 2003, BanTransFats.com Inc., a U.S. non-profit corporation, filed a lawsuit against the food manufacturer Kraft Foods in an attempt to force Kraft to remove trans fats from the Oreo cookie. The lawsuit was withdrawn when Kraft agreed to work on ways to find a substitute for the trans fat in the Oreo.

The J.M. Smucker Company, then the American manufacturer of Crisco (the original partially hydrogenated vegetable shortening), in 2004 released a new formulation made from solid saturated palm oil cut with soybean oil and sunflower oil. This blend yielded an equivalent shortening much like the prior partially hydrogenated Crisco, and was labelled zero grams of trans fat per 1 tablespoon serving (as compared with 1.5 grams per tablespoon of original Crisco). [169] As of 24 January 2007, Smucker claimed that all Crisco shortening products in the US have been reformulated to contain less than one gram of trans fat per serving while keeping saturated fat content less than butter. [170] The separately marketed trans fat free version introduced in 2004 was discontinued.

On 22 May 2004, Unilever, the corporate descendant of Joseph Crosfield & Sons (the original producer of Wilhelm Normann's hydrogenation hardened oils) announced that they have eliminated trans fats from all their margarine products in Canada, including their flagship Becel brand. [171]

Agribusiness giant Bunge Limited, through their Bunge Oils division, are now producing and marketing an NT product line of non-hydrogenated oils, margarines and shortenings, made from corn, canola, and soy oils. [172]

Since 2003, [173] Loders Croklaan, a wholly owned subsidiary of Malaysia's IOI Group has been providing trans fat free bakery and confectionery fats, made from palm oil, for giant food companies in the U.S. to make margarine. [174]

Major users' response

Beginning around 2000, as the scientific evidence and public concern about trans fat increased, major American users of trans fat began to switch to safer alternatives. The process received a large boost in 2003 when the FDA announced it would require trans fat labeling on packaged food starting in 2006. Packaged food companies then faced the choice of either eliminating trans fat from their products, or having to declare the trans fat on their nutrition label. Lawsuits in the U.S. against trans fat users also encouraged its removal.

Major American fast food chains including McDonald's, Burger King, KFC and Wendy's reduced and then removed partially hydrogenated oils (containing artificial trans fats) by 2009. This was a major step toward trans fat removal, as french fries were one of the largest sources of trans fat in the American diet, with a large fries typically having about 6 grams of trans fat until around 2007. [175] [176] [177] [178] [179] [180] [181] [182]

Two other events were important in the removal of trans fat. First, in 2013 the FDA announced it planned to completely ban artificial trans fat in the form of partially hydrogenated oil. Second, soon after this, Walmart informed its suppliers they needed to remove trans fat by 2015 if they wanted to continue to sell their products at its stores. As Walmart is the largest brick-and-mortar retailer in the U.S., mainstream food brands had little choice but to comply. [183]

These reformulations can be partly attributed to 2006 Center for Science in the Public Interest class action complaints, and to New York's restaurant trans fat ban, with companies such as McDonald's stating they would not be selling a unique product just for New York customers but would implement a nationwide or worldwide change. [184] [185] [186]

See also

Notes

Related Research Articles

<span class="mw-page-title-main">Fat</span> Esters of fatty acid or triglycerides

In nutrition, biology, and chemistry, fat usually means any ester of fatty acids, or a mixture of such compounds, most commonly those that occur in living beings or in food.

Essential fatty acids, or EFAs, are fatty acids that are required by humans and other animals for normal physiological function that cannot be synthesized in the body.⁠ As they are not synthesized in the body, the essential fatty acids – alpha-linolenic acid (ALA) and linoleic acid – must be obtained from food or from a dietary supplement. Essential fatty acids are needed for various cellular metabolic processes and for the maintenance and function of tissues and organs. These fatty acids also are precursors to vitamins, cofactors, and derivatives, including prostaglandins, leukotrienes, thromboxanes, lipoxins, and others.

α-Linolenic acid Chemical compound

α-Linolenic acid, also known as alpha-linolenic acid (ALA), is an n−3, or omega-3, essential fatty acid. ALA is found in many seeds and oils, including flaxseed, walnuts, chia, hemp, and many common vegetable oils.

<span class="mw-page-title-main">Margarine</span> Semi-solid oily spread often used as a butter substitute

Margarine is a spread used for flavoring, baking, and cooking. It is most often used as a substitute for butter. Although originally made from animal fats, most margarine consumed today is made from vegetable oil. The spread was originally named oleomargarine from Latin for oleum and Greek margarite. The name was later shortened to margarine.

<span class="mw-page-title-main">Coconut oil</span> Edible oil derived from coconut

Coconut oil is an edible oil derived from the kernels, meat, and milk of the coconut palm fruit. Coconut oil is a white solid fat below around 25 °C (77 °F), and a clear thin liquid oil at higher temperatures. Unrefined varieties have a distinct coconut aroma. Coconut oil is used as a food oil, and in industrial applications for cosmetics and detergent production. The oil is rich in medium-chain fatty acids.

Trans fat regulation, that aims to limit the amount of "trans fat" — fat containing trans fatty acids — in industrial food products, has been enacted in many countries. These regulations were motivated by numerous studies that pointed to significant negative health effects of trans fat. It is generally accepted that trans fat in the diet is a contributing factor in several diseases, including cardiovascular disease, diabetes, and cancer.

A saturated fat is a type of fat in which the fatty acid chains have all single bonds between the carbon atoms. A fat known as a glyceride is made of two kinds of smaller molecules: a short glycerol backbone and fatty acids that each contain a long linear or branched chain of carbon (C) atoms. Along the chain, some carbon atoms are linked by single bonds (-C-C-) and others are linked by double bonds (-C=C-). A double bond along the carbon chain can react with a pair of hydrogen atoms to change into a single -C-C- bond, with each H atom now bonded to one of the two C atoms. Glyceride fats without any carbon chain double bonds are called saturated because they are "saturated with" hydrogen atoms, having no double bonds available to react with more hydrogen.

An unsaturated fat is a fat or fatty acid in which there is at least one double bond within the fatty acid chain. A fatty acid chain is monounsaturated if it contains one double bond, and polyunsaturated if it contains more than one double bond.

<span class="mw-page-title-main">Cottonseed oil</span> Cooking oil

Cottonseed oil is cooking oil from the seeds of cotton plants of various species, mainly Gossypium hirsutum and Gossypium herbaceum, that are grown for cotton fiber, animal feed, and oil.

<span class="mw-page-title-main">Oleic acid</span> Monounsaturated omega-9 fatty acid

Oleic acid is a fatty acid that occurs naturally in various animal and vegetable fats and oils. It is an odorless, colorless oil, although commercial samples may be yellowish due to the presence of impurities. In chemical terms, oleic acid is classified as a monounsaturated omega-9 fatty acid, abbreviated with a lipid number of 18:1 cis-9, and a main product of Δ9-desaturase. It has the formula CH3−(CH2)7−CH=CH−(CH2)7−COOH. The name derives from the Latin word oleum, which means oil. It is the most common fatty acid in nature. The salts and esters of oleic acid are called oleates. It is a common component of oils, and thus occurs in many types of food, as well as in soap.

<span class="mw-page-title-main">Shortening</span> Food ingredient

Shortening is any fat that is a solid at room temperature and is used to make crumbly pastry and other food products.

In biochemistry and nutrition, a monounsaturated fat is a fat that contains a monounsaturated fatty acid (MUFA), a subclass of fatty acid characterized by having a double bond in the fatty acid chain with all of the remaining carbon atoms being single-bonded. By contrast, polyunsaturated fatty acids (PUFAs) have more than one double bond.

<span class="mw-page-title-main">Stanol ester</span> Class of chemical compounds

Stanol esters is a heterogeneous group of chemical compounds known to reduce the level of low-density lipoprotein (LDL) cholesterol in blood when ingested, though to a much lesser degree than prescription drugs such as statins. The starting material is phytosterols from plants. These are first hydrogenated to give a plant stanol which is then esterified with a mixture of fatty acids also derived from plants. Plant stanol esters are found naturally occurring in small quantities in fruits, vegetables, nuts, seeds, cereals, legumes, and vegetable oils.

The Center for Science in the Public Interest (CSPI) is a Washington, D.C.–based non-profit watchdog and consumer advocacy group that advocates for safer and healthier foods.

<span class="mw-page-title-main">Polyunsaturated fat</span> Type of fatty acid defined by molecular bonds

In biochemistry and nutrition, a polyunsaturated fat is a fat that contains a polyunsaturated fatty acid, which is a subclass of fatty acid characterized by a backbone with two or more carbon–carbon double bonds. Some polyunsaturated fatty acids are essentials. Polyunsaturated fatty acids are precursors to and are derived from polyunsaturated fats, which include drying oils.

<span class="mw-page-title-main">Western pattern diet</span> Modern dietary pattern

The Western pattern diet is a modern dietary pattern that is generally characterized by high intakes of pre-packaged foods, refined grains, red meat, processed meat, high-sugar drinks, candy and sweets, fried foods, industrially produced animal products, butter and other high-fat dairy products, eggs, potatoes, corn, and low intakes of fruits, vegetables, whole grains, pasture-raised animal products, fish, nuts, and seeds.

The chronic endothelial injury hypothesis is one of two major mechanisms postulated to explain the underlying cause of atherosclerosis and coronary heart disease (CHD), the other being the lipid hypothesis. Although an ongoing debate involving connection between dietary lipids and CHD sometimes portrays the two hypotheses as being opposed, they are in no way mutually exclusive. Moreover, since the discovery of the role of LDL cholesterol (LDL-C) in the pathogenesis of atherosclerosis, the two hypotheses have become tightly linked by a number of molecular and cellular processes.

A health claim found on a food labels and in food marketing is a claim by a food manufacturer that their product will reduce the risk of developing a disease or condition.

<span class="mw-page-title-main">Cooking oil</span> Oil consumed by humans, of vegetable or animal origin

Cooking oil is a plant or animal liquid fat used in frying, baking, and other types of cooking. Oil allows higher cooking temperatures than water, making cooking faster and more flavorful, while likewise distributing heat, reducing burning and uneven cooking. It sometimes imparts its own flavor. Cooking oil is also used in food preparation and flavoring not involving heat, such as salad dressings and bread dips.

<span class="mw-page-title-main">Fat hydrogenation</span> Addition of hydrogen atoms to fat molecules

Fat hydrogenation is the process of combining unsaturated fat with hydrogen in order to partially or completely convert it into saturated fat. Typically this hydrogenation is done with liquid vegetable oils resulting in solid or semi-solid fats.

References

  1. Gormley JJ, Juturu V (2010). "Partially Hydrogenated Fats in the US Diet and Their Role in Disease". In De Meester F, Zibadi S, Watson RR (eds.). Modern Dietary Fat Intakes in Disease Promotion. Nutrition and Health. Totowa, NJ: Humana Press. pp. 85–94. doi:10.1007/978-1-60327-571-2_5. ISBN   978-1-60327-571-2.
  2. EFSA Panel on Dietetic Products, Nutrition, and Allergies (NDA) (2010). "Scientific opinion on dietary reference values for fats". EFSA Journal. 8 (3): 1461. doi: 10.2903/j.efsa.2010.1461 .{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. UK Scientific Advisory Committee on Nutrition (2007). "Update on trans fatty acids and health, Position Statement" (PDF). Archived from the original on 13 April 2012. Retrieved 17 March 2024.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  4. Brouwer IA, Wanders AJ, Katan MB (March 2010). "Effect of animal and industrial trans fatty acids on HDL and LDL cholesterol levels in humans--a quantitative review". PLOS ONE. 5 (3): e9434. Bibcode:2010PLoSO...5.9434B. doi: 10.1371/journal.pone.0009434 . PMC   2830458 . PMID   20209147.
  5. "Trans fat". It's your health. Health Canada. Dec 2007. Archived from the original on 20 April 2012.
  6. "EFSA sets European dietary reference values for nutrient intakes" (Press release). European Food Safety Authority. 26 March 2010.
  7. "WHO plan to eliminate industrially-produced trans-fatty acids from global food supply" (Press release). World Health Organization. 14 May 2018.
  8. de Souza, Russell J.; Mente, Andrew; Maroleanu, Adriana; Cozma, Adrian I.; Ha, Vanessa; Kishibe, Teruko; Uleryk, Elizabeth; Budylowski, Patrick; Schünemann, Holger; Beyene, Joseph; Anand, Sonia S. (2015-08-11). "Intake of saturated and trans unsaturated fatty acids and risk of all cause mortality, cardiovascular disease, and type 2 diabetes: systematic review and meta-analysis of observational studies". BMJ (Clinical Research Ed.). 351: h3978. doi:10.1136/bmj.h3978. ISSN   1756-1833. PMC   4532752 . PMID   26268692.
  9. 1 2 Ghebreyesus TA, Frieden T (2021). "Eliminating trans fat from foods will save lives without changing the taste: Only our hearts will know the difference". World Health Organization. Retrieved 22 July 2023.
  10. Sergey Volkov (1 February 2024). "REPLACE Trans fat-free". World Health Organization. Retrieved 11 April 2024.
  11. "Butter, salted". FoodData Central. 2019-04-01. Retrieved 2024-10-11.
  12. 1 2 Alves, Susana P.; Vahmani, Payam; Mapiye, Cletos; McAllister, Tim A.; Bessa, Rui J. B.; Dugan, Michael E. R. (2021). "Trans-10 18:1 in ruminant meats: A review". Lipids. 32 (6): 539–562. doi:10.1002/lipd.12324. PMID   34608647. S2CID   238356805.
  13. Sarah K. Gebauer; Jean-Michel Chardigny; Marianne Uhre Jakobsen; Benoît Lamarche; Adam L. Lock; Spencer D. Proctor; David J. Baer (July 2011). "Effects of Ruminant trans Fatty Acids on Cardiovascular Disease and Cancer: A Comprehensive Review of Epidemiological, Clinical, and Mechanistic Studies". Advances in Nutrition. 2 (4): 332–354. doi: 10.3945/an.111.000521 . PMC   3125683 . PMID   22332075.
  14. Bassett CM, Edel AL, Patenaude AF, McCullough RS, Blackwood DP, Chouinard PY, et al. (January 2010). "Dietary vaccenic acid has antiatherogenic effects in LDLr-/- mice". The Journal of Nutrition. 140 (1): 18–24. doi: 10.3945/jn.109.105163 . PMID   19923390.
  15. Wang Y, Jacome-Sosa MM, Vine DF, Proctor SD (20 May 2010). "Beneficial effects of vaccenic acid on postprandial lipid metabolism and dyslipidemia: Impact of natural trans-fats to improve CVD risk". Lipid Technology. 22 (5): 103–106. doi:10.1002/lite.201000016.
  16. Baer, David J. (November 8–11, 2010). "New Findings on Dairy Trans Fat and Heart Disease Risk" (PDF). Auckland New Zealand. Archived from the original (PDF) on 2013-02-08. Retrieved 2023-05-26.
  17. Kuhnt K, Baehr M, Rohrer C, Jahreis G (October 2011). "Trans fatty acid isomers and the trans-9/trans-11 index in fat containing foods". European Journal of Lipid Science and Technology. 113 (10): 1281–1292. doi:10.1002/ejlt.201100037. PMC   3229980 . PMID   22164125.
  18. Teresa Tarrago-Trani, Maria; Phillips, Katherine M.; Lemar, Linda E.; Holden, Joanne M. (2006). "New and Existing Oils and Fats Used in Products with Reduced Trans-Fatty Acid Content" (PDF). Journal of the American Dietetic Association. 106 (6): 867–880. doi:10.1016/j.jada.2006.03.010. PMID   16720128.
  19. 1 2 Chatgilialoglu, Chryssostomos; Ferreri, Carla; Melchiorre, Michele; Sansone, Anna; Torreggiani, Armida (2014). "Lipid Geometrical Isomerism: From Chemistry to Biology and Diagnostics". Chemical Reviews. 114 (1): 255–284. doi: 10.1021/cr4002287 . PMID   24050531.
  20. 1 2 "About Trans Fat and Partially Hydrogenated Oils" (PDF). Center for Science in the Public Interest.
  21. 1 2 3 "Tentative Determination Regarding Partially Hydrogenated Oils". Federal Register. 8 November 2013. 2013-26854, Vol. 78, No. 217. Archived from the original on 6 April 2014. Retrieved 8 November 2013.
  22. de 141029 Process for converting unsaturated fatty acids or their glycerides into saturated compounds
  23. gb 190301515 Process for converting unsaturated fatty acids or their glycerides into saturated compounds
  24. Patterson HB (1998). "Hydrogenation" (PDF). Sci Lecture Papers Series. Archived from the original (PDF) on 26 September 2007. Retrieved 7 January 2007.
  25. 1 2 "Wilhelm Normann und die Geschichte der Fetthärtung von Martin Fiedler, 2001". 20 December 2011. Archived from the original on 1 October 2011. Retrieved 14 August 2007.
  26. Shurtleff, William; Aoyagi, Akiko. "History of Soybeans and Soyfoods: 1100 B.C. to the 1980s". Archived from the original on 18 October 2005.
  27. Kummerow, Fred A. (2008). Cholesterol Won't Kill You – But Trans Fat Could. Trafford Publishing. ISBN   978-1-4251-3808-0.
  28. 1 2 Schleifer D (January 2012). "The perfect solution: How trans fats became the healthy replacement for saturated fats". Technology and Culture. 53 (1): 94–119. doi:10.1353/tech.2012.0018. JSTOR   41475458. PMID   22530389. S2CID   26343964.
  29. Henderson GD (2015). "Re: The scientific report guiding the US dietary guidelines: is it scientific?". BMJ. 351: h4962. doi: 10.1136/bmj.h4962 . PMID   26400973. S2CID   42013152 . Retrieved 22 July 2023.
  30. Mary G. Enig. "The Tragic Legacy of Center for Science in the Public Interest (CSPI)" . Retrieved 22 July 2023.
  31. Ascherio A, Stampfer MJ, Willett WC (1999). "Trans fatty acids and coronary heart disease". The New England Journal of Medicine. 340 (25): 1994–1998. doi:10.1056/NEJM199906243402511. PMID   10379026. Archived from the original on 3 September 2006. Retrieved 14 September 2006.
  32. 1 2 Willett WC, Ascherio A (May 1994). "Trans fatty acids: are the effects only marginal?". American Journal of Public Health. 84 (5): 722–4. doi:10.2105/AJPH.84.5.722. PMC   1615057 . PMID   8179036.
  33. References:
  34. "Lawsuit dropped as Oreo looks to drop the fat". CNN. 14 May 2003. Retrieved 14 July 2011.
  35. "CSPI withdraws from lawsuit after KFC cuts trans fat". Centre for Science in the Public Interest. 2006. Retrieved 22 July 2023.
  36. L'Abbé MR, Stender S, Skeaff CM, Tavella M (2009). "Approaches to removing trans fats from the food supply in industrialized and developing countries". European Journal of Clinical Nutrition. 63 (Suppl 1): S50–7. doi: 10.1038/ejcn.2009.14 . PMC   2830089 . PMID   19190645.
  37. "Information Sheet: REPLACE trans fat: an action package to eliminate industrially produced trans-fatty acids". World Health Organization. 2021. Retrieved 22 July 2023.
  38. 1 2 Regulation: 21 CFR 101.9 (c)(2)(ii). Food and Drug Administration (11 July 2003). "21 CFR Part 101. Food labeling; trans fatty acids in nutrition labeling; consumer research to consider nutrient content and health claims and possible footnote or disclosure statements; final rule and proposed rule" (PDF). National Archives and Records Administration. Archived from the original (PDF) on 3 January 2007. Retrieved 18 January 2007.
  39. 1 2 "FDA acts to provide better information to consumers on trans fats". Food and Drug Administration. Archived from the original on 25 June 2005. Retrieved 26 July 2005.
  40. 1 2 "Newswise: most consumers misinterpret meaning of trans fat information on Nutrition Facts panel" . Retrieved 19 June 2008.
  41. 1 2 Shockman, Luke (5 December 2005). "Trans fat: 'Zero' foods add up". Toledo Blade. Archived from the original on 21 June 2009. Retrieved 18 January 2007.
  42. Casimir C. Akoh; David B. Min., eds. (2002). Food lipids: chemistry, nutrition, and biotechnology. New York: M. Dekker. pp. 1–2. ISBN   978-0-8247-0749-1.
  43. ""fatty acid"". IUPAC Gold book. International Union of Pure and Applied Chemistry. 2014. doi:10.1351/goldbook.F02330.
  44. Alonso L, Fontecha J, Lozada L, Fraga MJ, Juárez M (May 1999). "Fatty acid composition of caprine milk: major, branched-chain, and trans fatty acids". Journal of Dairy Science. 82 (5): 878–84. doi: 10.3168/jds.S0022-0302(99)75306-3 . hdl:10261/113439. PMID   10342226.
  45. Thomas, Alfred (2002). "Fats and Fatty Oils". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_173. ISBN   978-3-527-30673-2.
  46. Martin CA, Milinsk MC, Visentainer JV, Matsushita M, de-Souza NE (June 2007). "Trans fatty acid-forming processes in foods: a review". Anais da Academia Brasileira de Ciências. 79 (2): 343–50. doi: 10.1590/S0001-37652007000200015 . PMID   17625687.
  47. Udo Erasmus; Fats that heal, Fats that Kill, Alive books, 1993 edition, Pages 13-19.
  48. 1 2 "Section 7: Biochemistry". Handbook of chemistry and physics. 2007–2008 (88th ed.). Taylor and Francis. 2007. Archived from the original (PDF) on 24 July 2017. Retrieved 19 November 2007.
  49. Eller FJ, List GR, Teel JA, Steidley KR, Adlof RO (July 2005). "Preparation of spread oils meeting U.S. Food and Drug Administration Labeling requirements for trans fatty acids via pressure-controlled hydrogenation". Journal of Agricultural and Food Chemistry. 53 (15): 5982–4. doi:10.1021/jf047849+. PMID   16028984.
  50. Tarrago-Trani MT, Phillips KM, Lemar LE, Holden JM (June 2006). "New and existing oils and fats used in products with reduced trans-fatty acid content". Journal of the American Dietetic Association. 106 (6): 867–80. doi:10.1016/j.jada.2006.03.010. PMID   16720128.
  51. 1 2 Mozaffarian, Dariush; Katan, Martijn B.; Ascherio, Alberto; Stampfer, Meir J.; Willett, Walter C. (2006). "Trans Fatty Acids and Cardiovascular Disease". New England Journal of Medicine. 354 (15): 1601–1613. doi:10.1056/NEJMra054035. PMID   16611951.
  52. 1 2 3 4 Trans Fat Task Force (June 2006). TRANSforming the Food Supply. Trans Fat Task Force. ISBN   0-662-43689-X . Retrieved 7 January 2007.
  53. Ashok, Chauhan; Ajit, Varma (2009). "Chapter 4: Fatty acids". A Textbook of Molecular Biotechnology. I. K. International Pvt. p. 181. ISBN   978-93-80026-37-4.
  54. Hunter JE (2005). "Dietary levels of trans fatty acids" basis for health concerns and industry efforts to limit use". Nutrition Research. 25 (5): 499–513. doi:10.1016/j.nutres.2005.04.002.
  55. Innis SM, King DJ (September 1999). "trans Fatty acids in human milk are inversely associated with concentrations of essential all-cis n-6 and n-3 fatty acids and determine trans, but not n-6 and n-3, fatty acids in plasma lipids of breast-fed infants". The American Journal of Clinical Nutrition. 70 (3): 383–90. doi: 10.1093/ajcn/70.3.383 . PMID   10479201.
  56. NYC Board of Health. "Board of Health Approves Regulation to Phase Out Artificial Trans Fat: FAQ". Archived from the original on 6 October 2006. Retrieved 7 January 2007.
  57. "What's in that french fry? Fat varies by city". NBC News. 12 April 2006. Retrieved 7 January 2007.[ dead link ] AP story concerning Stender, S; Dyerberg, J; Astrup, A (April 2006). "High levels of industrially produced trans fat in popular fast foods". N. Engl. J. Med. 354 (15): 1650–2. doi: 10.1056/NEJMc052959 . PMID   16611965.
  58. Food and nutrition board, institute of medicine of the national academies (2005). Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients). National Academies Press. p. i. Archived from the original on 18 September 2006.
  59. Food and nutrition board, institute of medicine of the national academies (2005). Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein, and amino acids (macronutrients). National Academies Press. pp.  423. doi:10.17226/10490. ISBN   978-0-309-08525-0.
  60. Food and nutrition board, institute of medicine of the national academies (2005). Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients). National Academies Press. p. 447.[ permanent dead link ]
  61. 1 2 3 Food and nutrition board, institute of medicine of the national academies (2005). Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein, and amino acids (macronutrients). National Academies Press. p. 504.[ permanent dead link ]
  62. 1 2 3 4 Mozaffarian D, Katan MB, Ascherio A, Stampfer MJ, Willett WC (April 2006). "Trans fatty acids and cardiovascular disease". The New England Journal of Medicine. 354 (15): 1601–13. doi:10.1056/NEJMra054035. PMID   16611951. S2CID   35121566.
  63. Food and nutrition board, institute of medicine of the national academies (2005). Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients). National Academies Press. p. 424.[ permanent dead link ]
  64. National Dairy Council (18 June 2004). "comments on 'Docket No. 2003N-0076 Food Labeling: Trans Fatty Acids in Nutrition Labeling'" (PDF). Retrieved 7 January 2007.{{cite journal}}: Cite journal requires |journal= (help)
  65. Brouwer IA, Wanders AJ, Katan MB (March 2010). Reitsma PH (ed.). "Effect of animal and industrial trans fatty acids on HDL and LDL cholesterol levels in humans--a quantitative review". PLOS ONE. 5 (3): e9434. Bibcode:2010PLoSO...5.9434B. doi: 10.1371/journal.pone.0009434 . PMC   2830458 . PMID   20209147.
  66. Tricon S, Burdge GC, Kew S, Banerjee T, Russell JJ, Jones EL, et al. (September 2004). "Opposing effects of cis-9,trans-11 and trans-10,cis-12 conjugated linoleic acid on blood lipids in healthy humans". The American Journal of Clinical Nutrition. 80 (3): 614–20. doi: 10.1093/ajcn/80.3.614 . PMID   15321800.
  67. Zulet MA, Marti A, Parra MD, Martínez JA (September 2005). "Inflammation and conjugated linoleic acid: mechanisms of action and implications for human health". Journal of Physiology and Biochemistry. 61 (3): 483–94. doi:10.1007/BF03168454. PMID   16440602. S2CID   32082565.
  68. 1 2 Valenzuela A, Morgado N (1999). "Trans fatty acid isomers in human health and in the food industry". Biological Research. 32 (4): 273–87. doi: 10.4067/s0716-97601999000400007 . PMID   10983247.
  69. Kummerow FA, Zhou Q, Mahfouz MM, Smiricky MR, Grieshop CM, Schaeffer DJ (April 2004). "Trans fatty acids in hydrogenated fat inhibited the synthesis of the polyunsaturated fatty acids in the phospholipid of arterial cells". Life Sciences. 74 (22): 2707–23. doi:10.1016/j.lfs.2003.10.013. PMID   15043986.
  70. Mojska H (2003). "Influence of trans fatty acids on infant and fetus development". Acta Microbiologica Polonica. 52 Suppl: 67–74. PMID   15058815.
  71. Koletzko B, Decsi T (October 1997). "Metabolic aspects of trans fatty acids". Clinical Nutrition. 16 (5): 229–37. doi:10.1016/s0261-5614(97)80034-9. PMID   16844601.
  72. Menaa F, Menaa A, Menaa B, Tréton J (June 2013). "Trans-fatty acids, dangerous bonds for health? A background review paper of their use, consumption, health implications and regulation in France". European Journal of Nutrition. 52 (4): 1289–302. doi:10.1007/s00394-012-0484-4. PMID   23269652. S2CID   206968361.
  73. Riserus, Ulf (2006). "Trans fatty acids, insulin sensitivity and type 2 diabetes". Scandinavian Journal of Food and Nutrition. 50 (4): 161–165. doi: 10.1080/17482970601133114 .
  74. 1 2 3 4 Trans Fat Task Force (June 2006). "TRANSforming the Food Supply (Appendix 9iii)". Archived from the original on 25 February 2007. Retrieved 9 January 2007.{{cite journal}}: Cite journal requires |journal= (help) (Consultation on the health implications of alternatives to trans fatty acids: Summary of Responses from Experts)
  75. Zaloga GP, Harvey KA, Stillwell W, Siddiqui R (October 2006). "Trans fatty acids and coronary heart disease". Nutrition in Clinical Practice. 21 (5): 505–12. doi:10.1177/0115426506021005505. PMID   16998148.
  76. 1 2 Hu FB, Stampfer MJ, Manson JE, Rimm E, Colditz GA, Rosner BA, et al. (November 1997). "Dietary fat intake and the risk of coronary heart disease in women". The New England Journal of Medicine. 337 (21): 1491–9. doi: 10.1056/NEJM199711203372102 . PMID   9366580.
  77. Oh K, Hu FB, Manson JE, Stampfer MJ, Willett WC (April 2005). "Dietary fat intake and risk of coronary heart disease in women: 20 years of follow-up of the nurses' health study". American Journal of Epidemiology. 161 (7): 672–9. doi: 10.1093/aje/kwi085 . PMID   15781956.
  78. Ascherio A, Katan MB, Zock PL, Stampfer MJ, Willett WC (June 1999). "Trans fatty acids and coronary heart disease". The New England Journal of Medicine. 340 (25): 1994–8. doi:10.1056/NEJM199906243402511. PMID   10379026. S2CID   30165590.
  79. Mensink RP, Katan MB (August 1990). "Effect of dietary trans fatty acids on high-density and low-density lipoprotein cholesterol levels in healthy subjects". The New England Journal of Medicine. 323 (7): 439–45. doi: 10.1056/NEJM199008163230703 . PMID   2374566.
  80. Mensink RP, Zock PL, Kester AD, Katan MB (May 2003). "Effects of dietary fatty acids and carbohydrates on the ratio of serum total to HDL cholesterol and on serum lipids and apolipoproteins: a meta-analysis of 60 controlled trials". The American Journal of Clinical Nutrition. 77 (5): 1146–55. doi: 10.1093/ajcn/77.5.1146 . PMID   12716665.
  81. Gatto LM, Sullivan DR, Samman S (May 2003). "Postprandial effects of dietary trans fatty acids on apolipoprotein(a) and cholesteryl ester transfer". The American Journal of Clinical Nutrition. 77 (5): 1119–24. doi:10.1093/ajcn/77.5.1119. PMID   12716661.
  82. Lopez-Garcia E, Schulze MB, Meigs JB, Manson JE, Rifai N, Stampfer MJ, et al. (March 2005). "Consumption of trans fatty acids is related to plasma biomarkers of inflammation and endothelial dysfunction". The Journal of Nutrition. 135 (3): 562–6. doi: 10.1093/jn/135.3.562 . PMID   15735094.
  83. Morris MC, Evans DA, Bienias JL, Tangney CC, Bennett DA, Aggarwal N, et al. (February 2003). "Dietary fats and the risk of incident Alzheimer disease". Archives of Neurology. 60 (2): 194–200. doi:10.1001/archneur.60.2.194. PMID   12580703.
  84. 1 2 Phivilay A, Julien C, Tremblay C, Berthiaume L, Julien P, Giguère Y, Calon F (March 2009). "High dietary consumption of trans fatty acids decreases brain docosahexaenoic acid but does not alter amyloid-beta and tau pathologies in the 3xTg-AD model of Alzheimer's disease". Neuroscience. 159 (1): 296–307. doi:10.1016/j.neuroscience.2008.12.006. PMID   19135506. S2CID   35748183.
  85. Granholm AC, Bimonte-Nelson HA, Moore AB, Nelson ME, Freeman LR, Sambamurti K (June 2008). "Effects of a saturated fat and high cholesterol diet on memory and hippocampal morphology in the middle-aged rat". Journal of Alzheimer's Disease. 14 (2): 133–45. doi:10.3233/JAD-2008-14202. PMC   2670571 . PMID   18560126.
  86. Nwaru BI, Dierkes J, Ramel A, Arnesen EK, Thorisdottir B, Lamberg-Allardt C, Söderlund F, Bärebring L, Åkesson A (2022). "Quality of dietary fat and risk of Alzheimer's disease and dementia in adults aged ≥50 years: a systematic review". Food & Nutrition Research. 66. doi:10.29219/fnr.v66.8629. PMC   9338447 . PMID   35950105.
  87. American Cancer Society. "Common questions about diet and cancer". Archived from the original on 13 April 2010. Retrieved 9 January 2007.
  88. Chavarro J, Stampfer M, Campos H, Kurth T, Willett W, Ma J (1 April 2006). "A prospective study of blood trans fatty acid levels and risk of prostate cancer". Proc. Amer. Assoc. Cancer Res. 47 (1): 943. Retrieved 9 January 2007.
  89. Brasky TM, Till C, White E, Neuhouser ML, Song X, Goodman P, et al. (June 2011). "Serum phospholipid fatty acids and prostate cancer risk: results from the prostate cancer prevention trial". American Journal of Epidemiology. 173 (12): 1429–39. doi:10.1093/aje/kwr027. PMC   3145396 . PMID   21518693.
  90. "Breast cancer: a role for trans fatty acids?". World Health Organization (Press release). 11 April 2008. Archived from the original on 13 April 2008.
  91. Chajès V, Thiébaut AC, Rotival M, Gauthier E, Maillard V, Boutron-Ruault MC, et al. (June 2008). "Association between serum trans-monounsaturated fatty acids and breast cancer risk in the E3N-EPIC Study". American Journal of Epidemiology. 167 (11): 1312–20. doi:10.1093/aje/kwn069. PMC   2679982 . PMID   18390841.
  92. Hu FB, van Dam RM, Liu S (July 2001). "Diet and risk of Type II diabetes: the role of types of fat and carbohydrate". Diabetologia. 44 (7): 805–17. doi: 10.1007/s001250100547 . PMID   11508264.
  93. van Dam RM, Willett WC, Rimm EB, Stampfer MJ, Hu FB (March 2002). "Dietary fat and meat intake in relation to risk of type 2 diabetes in men". Diabetes Care. 25 (3): 417–24. doi: 10.2337/diacare.25.3.417 . PMID   11874924.
  94. Gosline, Anna (12 June 2006). "Why fast foods are bad, even in moderation". New Scientist . Retrieved 9 January 2007.
  95. "Six years of fast-food fats supersizes monkeys". New Scientist (2556): 21. 17 June 2006.
  96. 1 2 Kavanagh K, Jones KL, Sawyer J, Kelley K, Carr JJ, Wagner JD, Rudel LL (July 2007). "Trans fat diet induces abdominal obesity and changes in insulin sensitivity in monkeys". Obesity. 15 (7): 1675–84. doi: 10.1038/oby.2007.200 . PMID   17636085. S2CID   4835948.
  97. Thompson, Tommy G. "Trans Fat Press Conference". Archived from the original on 9 July 2006., US Secretary of health and human services
  98. Mahfouz M (1981). "Effect of dietary trans fatty acids on the delta 5, delta 6 and delta 9 desaturases of rat liver microsomes in vivo". Acta Biologica et Medica Germanica. 40 (12): 1699–1705. PMID   7345825.
  99. Chavarro JE, Rich-Edwards JW, Rosner BA, Willett WC (January 2007). "Dietary fatty acid intakes and the risk of ovulatory infertility". The American Journal of Clinical Nutrition. 85 (1): 231–7. doi: 10.1093/ajcn/85.1.231 . PMID   17209201.
  100. Roan, Shari (28 January 2011). "Trans fats and saturated fats could contribute to depression". The Sydney Morning Herald. Retrieved 8 February 2011.
  101. McNamara RK, Hahn CG, Jandacek R, Rider T, Tso P, Stanford KE, Richtand NM (July 2007). "Selective deficits in the omega-3 fatty acid docosahexaenoic acid in the postmortem orbitofrontal cortex of patients with major depressive disorder". Biological Psychiatry. 62 (1): 17–24. doi:10.1016/j.biopsych.2006.08.026. PMID   17188654. S2CID   32898004.
  102. Golomb BA, Evans MA, White HL, Dimsdale JE (2012). "Trans fat consumption and aggression". PLOS ONE. 7 (3): e32175. Bibcode:2012PLoSO...732175G. doi: 10.1371/journal.pone.0032175 . PMC   3293881 . PMID   22403632.
  103. Golomb BA, Bui AK (2015). "A Fat to Forget: Trans Fat Consumption and Memory". PLOS ONE. 10 (6): e0128129. Bibcode:2015PLoSO..1028129G. doi: 10.1371/journal.pone.0128129 . PMC   4470692 . PMID   26083739.
  104. Melnik BC (15 July 2015). Weinberg J (ed.). "Linking diet to acne metabolomics, inflammation, and comedogenesis: an update". Clinical, Cosmetic and Investigational Dermatology. 8: 371–88. doi: 10.2147/CCID.S69135 . PMC   4507494 . PMID   26203267.
  105. "Codex Stan 19-1999" (PDF). Archived from the original (PDF) on 2012-02-29. Retrieved 2021-05-27.
  106. Codex Stan 256–2007 "Standard for Fat Spreads and Blended Spreads" Archived 2012-02-29 at the Wayback Machine (PDF file)
  107. "WHO plan to eliminate industrially-produced trans-fatty acids from global food supply". WHO. 14 May 2018. Retrieved 15 August 2018.
  108. "Joint resolution SPRyRS 149/2005 and SAGPyA 683/2005" (PDF). Archived from the original (PDF) on 2021-07-01. Retrieved 2021-05-27.
  109. "Un corte al colesterol". Página/12. 21 December 2010.
  110. "Argentina Celebrates New Year Free of Trans Fats". IPS News . 3 January 2015.
  111. "Fast food outlets asked to cut down trans fat usage". ABC. 12 March 2007. Archived from the original on 8 March 2009. Retrieved 12 March 2007.
  112. Clifton PM, Keogh JB, Noakes M (April 2004). "Trans fatty acids in adipose tissue and the food supply are associated with myocardial infarction". The Journal of Nutrition. 134 (4): 874–9. doi: 10.1093/jn/134.4.874 . PMID   15051840.
  113. "Bundesgesetzblatt Für Die Republik Österreich" (PDF). BMG. Archived from the original (PDF) on 7 September 2012. Retrieved 7 November 2013.
  114. Conseil Supérieur de la Santé, ed. (July 2012). "acides gras trans d'origine industrielle" (PDF). Avis du Conseil Supérieur de la Santé N° 8666. Retrieved 11 December 2015.
  115. "Publicada norma sobre gordura trans em alimentos". Portal ANVISA. ANVISA. 27 December 2019. Retrieved 28 April 2020.
  116. "A gorduras trans que você não vê" (in Portuguese). iDEC. Retrieved 2024-06-19.
  117. "Health Canada trans fat ban takes effect next year". CBC News. 15 September 2017.
  118. "Canadian Ban on Trans Fats Comes into Force Today". Government of Canada. Health Canada. 17 September 2018. Retrieved 3 October 2019.
  119. Nasser R, Cook S, Bashutski M, Hill K, Norton D, Coleman J, et al. (August 2011). "Consumer perceptions of trans fats in 2009 show awareness of negative effects but limited concern regarding use in snack foods". Applied Physiology, Nutrition, and Metabolism. 36 (4): 526–32. doi:10.1139/h11-045. PMID   21854161.
  120. "Trans Fat Regulation". News-Medical.Net. 1 January 2008. Retrieved 21 June 2013.
  121. Stender S, Dyerberg J, Bysted A, Leth T, Astrup A (May 2006). "A trans world journey". Atherosclerosis. Supplements. 7 (2): 47–52. doi:10.1016/j.atherosclerosissup.2006.04.011. PMID   16713385.
  122. Stender S, Dyerberg J (2004). "Influence of trans fatty acids on health". Annals of Nutrition & Metabolism. 48 (2): 61–6. doi:10.1159/000075591. PMID   14679314. S2CID   13293130.
  123. "Opinion of the Scientific Panel on Dietetic products, nutrition and allergies (NDA) related to the presence of trans fatty acids in foods and the effect on human health of the consumption of trans fatty acids. Question number: EFSA-Q-2003-022". 2004. Retrieved 20 February 2009.
  124. BINNS, John (2019-04-24). "Trans fat in food". Food Safety - European Commission. Retrieved 2019-06-13.
  125. ΕΦΕΤ (May 2015). "Γνώσεις, στάση και συμπεριφορά των Ελλήνων σχετικά με τα τρανς λιπαρά" (PDF). Archived from the original (PDF) on 2017-12-15.
  126. Fridleifsdottir, Siv (11 November 2010). "New Icelandic rules for trans fats". The Nordic Council. Archived from the original on 17 January 2011. Retrieved 21 June 2013.
  127. "New Icelandic rules for trans fats". Ríkisútvarpið. 22 December 2010. Archived from the original on 28 January 2015. Retrieved 27 May 2021.
  128. "נכנסה לתוקף בישראל חובת סימון שומן טראנס על גבי אריזות מזון ארוז". health.gov.il.
  129. DOH reminds food firms: Eliminate trans fat by June 2023
  130. "SFDA Applied Strict Measures to Reduce Consumption of "Trans Fats"". Saudi Food & Drug Agency. Archived from the original on 28 December 2018. Retrieved 27 December 2018.
  131. @tfrabiah (December 6, 2018). "بعد ١٣ شهراً (في ١-١-٢٠٢٠) سوف" (Tweet). Archived from the original on 2018-12-21. Retrieved 2023-05-26 via Twitter.
  132. Choo, Felicia (6 March 2019). "MOH to ban artificial trans fat in cookies and noodles". The Straits Times. Retrieved 7 March 2019.
  133. Kurohi, Rei (6 June 2019). "MOH to ban key source of artificial trans fats in food like cookies and pizzas from June 2021". The Straits Times. Retrieved 28 September 2019.
  134. Riksdagsförvaltningen. "Livsmedelskontroll". riksdagen.se.
  135. Dagens Nyheter (20 September 2013). "Svenska butiker i transfett-topp". Svenska Dagbladet.
  136. "Deadly fats: why are we still eating them?". The Independent. London. 10 June 2008. Retrieved 16 June 2008.
  137. Gray, Richard (5 February 2006). "Forced to own up to the killer fat in our food". The Scotsman. Edinburgh. Retrieved 18 January 2007.
  138. "Call to label hidden fats in food". BBC. 20 July 2006. Retrieved 18 January 2007. reporting on Clarke R, Lewington S (July 2006). "Trans fatty acids and coronary heart disease". BMJ. 333 (7561): 214. doi:10.1136/bmj.333.7561.214. PMC   1523500 . PMID   16873835.
  139. "Waitrose position on Hydrogenated Vegetable Oils / Transfats" (Press release). 22 Jun 2010. Waitrose eliminated the use of hydrogenated vegetable oils in all own label products by the end of 2006.
  140. "Retailers to stop trans-fat use". BBC. 31 January 2007. Retrieved 31 January 2007.
  141. Food Standards Agency (13 December 2007). Board recommends voluntary approach for trans fats Archived 2012-04-12 at the Wayback Machine .
  142. Food Standards Agency (13 December 2007).FSA Board to advise the Department of Health to maintain successful voluntary approach for trans fats in food Archived 2011-12-06 at the Wayback Machine .
  143. Mozaffarian D, Stampfer MJ (April 2010). "Removing industrial trans fat from foods". BMJ. 340: c1826. doi:10.1136/bmj.c1826. PMID   20395265. S2CID   25364298.
  144. National Institute for Health and Clinical Excellence (June 2010), "Recommendations", NICE public health guidance 25: Prevention of cardiovascular disease, Manchester, UK, p. 31, archived from the original on 11 December 2014, retrieved 17 June 2015{{citation}}: CS1 maint: location missing publisher (link)
  145. Lincoln, Paul, NICE CVD guidance expert testimony paper 9, pp. 2, 7, archived from the original on 17 June 2015, retrieved 17 June 2015
  146. Maeve, McClenaghan. "Analysis: Unhealthy friendships with Department of Health". Bureau of Investigative Journalism. Archived from the original on 17 October 2015. Retrieved 4 January 2013.
  147. Hogg, Clare Dwyer (10 September 2011). "Dying for a burger? Why are trans fats still legal in the UK?". The Independent. Retrieved 31 December 2012.
  148. "Revealing Trans Fats". Federal Citizen Information Center. U.S. Food and Drug Administration. 2010-03-11. Archived from the original on 2010-03-11. Retrieved 2023-02-07.
  149. 301. Mono- and diglycerides (WHO Food Additives Series 5). Joint FAO/WHO Expert Committee on Food Additives. FAO Nutrition Meetings Report Series. Geneva. 1974. Retrieved 2023-02-07.
  150. Misko, George (1 October 2003). "FDA requires trans fatty acid labeling for foods and dietary supplements". Allbusiness.com. Archived from the original on 29 March 2008. Retrieved 14 July 2011.
  151. Food and Drug Administration (11 July 2003). "FDA food labeling: trans fatty acids in nutrition labeling; consumer research to consider nutrient content and health claims and possible footnote or disclosure statements". p. 41059. Archived from the original on 19 December 2006. Retrieved 18 January 2007.
  152. 1 2 American Public Health Association. "Restricting trans fatty acids in the food supply". Archived from the original on 6 May 2008. Retrieved 28 February 2008.
  153. "AMA supports trans-fat bans". Reuters. 11 November 2008. Archived from the original on 12 May 2012. Retrieved 14 July 2011.
  154. 1 2 Dennis, Brady (2 June 2017). "Fred Kummerow, U. of I. professor who fought against trans fats, dies at 102". Chicago Tribune. Retrieved 2023-02-07.
  155. Watson, Elaine (13 August 2013). "Researcher files lawsuit vs FDA after it ignored his petition calling for ban on artificial trans fats". Food Navigator USA.
  156. Lopez, Ricardo (7 November 2013). "Citing health risks, FDA moves to virtually eliminate trans fat". Los Angeles Times.
  157. "FDA targets trans fat in processed foods". US Food and Drug Administration. 7 November 2013. Retrieved 7 November 2013.
  158. Christensen, Jen (16 June 2015). "FDA orders food manufacturers to stop using trans fat within three years". CNN. Retrieved 16 June 2015.
  159. Dennis, Brady (16 June 2015). "FDA moves to ban trans fat from U.S. food supply". The Washington Post.
  160. 1 2 Hafner, Katie (2017-06-01). "Fred A. Kummerow, an Early Opponent of Trans Fats, Dies at 102". The New York Times. ISSN   0362-4331 . Retrieved 2023-02-07.
  161. "Final Determination Regarding Partially Hydrogenated Oils". 17 June 2015.
  162. Christensen, Jen. "FDA orders food manufacturers to stop using trans fat within three years". CNN.
  163. "Final Determination Regarding Partially Hydrogenated Oils". Federal Register. 2015-06-17. Retrieved 2021-06-08.
  164. Dennis, Brady (16 June 2015). "The 100-year-old scientist who pushed the FDA to ban artificial trans fat". The Washington Post.
  165. Edney, Anna; Giammona, Craig (16 June 2015). "U.S. Bans Trans Fat". Bloomberg L.P.
  166. Dewey, Caitlin (18 June 2018). "Analysis | Artificial trans fats, widely linked to heart disease, are officially banned". Washington Post. ISSN   0190-8286 . Retrieved 18 June 2018.
  167. Vega-López S, Ausman LM, Jalbert SM, Erkkilä AT, Lichtenstein AH (July 2006). "Palm and partially hydrogenated soybean oils adversely alter lipoprotein profiles compared with soybean and canola oils in moderately hyperlipidemic subjects". The American Journal of Clinical Nutrition. 84 (1): 54–62. doi: 10.1093/ajcn/84.1.54 . PMID   16825681.
  168. "Palm oil not a healthy substitute for trans fats, study finds". ScienceDaily. 11 May 2009. Retrieved 12 May 2010.
  169. "Crisco 0 grams trans fat per serving all-vegetable shortening". Archived from the original on 15 October 2006. Retrieved 18 January 2007.
  170. " "Crisco Frequently Asked Questions". Archived from the original on 27 September 2007.
  171. "List of Canadian industry actions to reduce transfats". Food & Consumer Products of Canada (FCPC). Archived from the original on 27 September 2007. Retrieved 13 September 2007.
  172. "Welcome to TransFatSolutions.com powered by Bunge". Transfatsolutions.com. Retrieved 14 July 2011.
  173. "Loders builds on trans fat alternatives". Foodnavigator.com. 5 February 2004. Retrieved 7 December 2010.
  174. Fletcher, Anthony (10 November 2005). "Loders Croklaan targets trans fat free demand". Food Navigator.
  175. Urban, Lorien E. (2014). "Temporal Trends in Fast-Food Restaurant Energy, Sodium, Saturated Fat, and Trans Fat Content, United States, 1996–2013". Preventing Chronic Disease. 11: E229. doi:10.5888/pcd11.140202. ISSN   1545-1151. PMC   4283359 . PMID   25551184.
  176. "Trans Fat Food Industry Response". News-Medical.net. 24 March 2010.
  177. "KFC Sued for Fouling Chicken with Partially Hydrogenated Oil: Lawsuit Aimed at Eliminating, or Disclosing Use of Artery-Clogging Frying Oil" (Press release). Center for Science in the Public Interest. 12 June 2006. Retrieved 18 January 2007.
  178. "Class action complaint" (PDF). 12 June 2006. Retrieved 18 January 2007.
  179. Burros, Marian (14 June 2006). "KFC Is Sued Over the Use of Trans Fats in Its Cooking". The New York Times. Retrieved 18 January 2007.
  180. "KFC announces switch to zero trans fat cooking oil following two-year test for same great taste" (Press release). KFC. 30 October 2006. Archived from the original on 19 January 2007. Retrieved 18 January 2007.
  181. "KFC Canada phasing in zero grams trans fat menu in all 786 restaurants nationally early in the new year" (Press release). KFC Canada. 30 October 2006. Archived from the original on 18 February 2007. Retrieved 18 January 2007.
  182. "Wendy's Significantly Cuts Trans Fats – Switch to New Cooking Oil Under Way" (Press release). Wendy's. 8 June 2006. Archived from the original on 9 November 2006. Retrieved 11 April 2013.
  183. "McDonald's finally picks trans-fat-free oil". NBC News. 30 January 2007.[ dead link ]
  184. "Chick-fil-A Removes Trans Fats from Menu" (Press release). NBC News. 10 October 2008.
  185. Sainz, Adrian (6 July 2006). "Burger King to Use Trans-Fat-Free Oil" (Press release). Associated Press. Archived from the original on 29 September 2007. Retrieved 6 July 2007.
  186. Nutrition Information Archived 21 July 2015 at the Wayback Machine . Ihop.com (2015). Retrieved 22 August 2015.

Further reading