Journal of Diabetes Science and Technology

Last updated

Abstracting and indexing

The journal is abstracted and indexed in Index Medicus/MEDLINE/PubMed [1] and Scopus. [2]

Special sections

Volume 1 (2007)

Issue 1 - Journal of Diabetes Science and Technology and the Diabetes Technology Community [3]

Issue 3 - Mathematical Models of the Metabolic System in Health and in Diabetes [4]

Issue 4 - Optical Non-Invasive Glucose Monitoring [5]

Issue 5 - Sensors & Algorithms for Continuous Glucose Monitoring [6]

Issue 6 - Artificial Pancreas: Closed-Loop Control of Glucose Variability in Diabetes [7]

Volume 2 (2008)

Issue 1 - Technology for Diabetes Care and Evaluation in the Veterans Health Administration [8]

Issue 2 - Automated Inpatient Blood Sampling for Glucose Measurement [9]

Issue 3 - Computerized Algorithms [10]

Issue 4 - No-Coding Strategies for Glucose Monitors [11]

Issue 5 - Biocompatibility of Implanted Diabetes Devices: Part 1 [12]

Issue 6 - Technology for Hospital Management of Diabetes [13]

Volume 3 (2009)

Issue 2 - Non-Invasive Technologies for Glucose Monitoring [14]

Issue 3 - Laboratory Advances in Hemoglobin A1c Measurement [15]

Issue 4 - Clinical Advances in Hemoglobin A1c Measurement [16]

Issue 5 - Artificial Pancreas Systems [17]

Issue 6 - Challenges in Glycemic Control in Perioperative and Critically Ill Patients [18]

Volume 4 (2010)

Issue 1 - Alarms for Continuous Glucose Monitors [19]

Issue 2 - Blood Spot Testing Symposium [20]

Issue 3 - Insulin Pens [21]

Issue 4 - Foot Technology [22]

Issue 5 - Interstitial Fluid Physiology as it Relates to Glucose Monitoring Technologies [23]

Issue 6 - Glucagon: Physiology and Pharmacotherapy [24]

Volume 5 (2011)

Issue 1 - Mobile Technology [25]

Issue 2 - Virtual Reality Technologies for Research and Education in Obesity and Diabetes - Sponsored by the National Institutes of Health [26]

Issue 3 - Interstitial Fluid Physiology as It Relates to Glucose Monitoring Technologies [27]

Issue 4 - Diabetes and the Environment [28]

Issue 5 - Glucose Electrochemistry [29]

Issue 6 - Artificial Pancreas [30]

Volume 6 (2012)

Issue 1 - Management of Hyperglycemia in the Pediatric ICU [31]

Issue 2 - Human Factors for Diabetes Devices [32]

Issue 3 - Diabetes Mellitus in Veterinary Medicine [33]

Issue 4 - Ultra-Fast Insulins [34]

Issue 5 - Diabetes Technologies and Hospital Care [35]

Issue 6 - Fluorescence Glucose Sensing, Part I [36]

Volume 7 (2013)

Issue 2 - Legal Issues in Diabetes Technologies [37]

Issue 3 - Mobile Health and Diabetes [38]

Volume 8 (2014)

Issue 1 - Biosimilar Insulin [39]

Issue 2 - Telemedicine for Diabetes [40]

Issue 3 - Novel Methods for Delivering Insulin [41]

Issue 4 - Hospital Diabetes Software Part 1 [42]

Issue 5 - Hospital Diabetes Software, Part 2 [43]

Issue 6 - Hospital Diabetes Hardware [44]

Volume 9 (2015)

Issue 1 - Glucagon Therapy [45]

Issue 2 - Glycated Proteins [46]

Issue 3 - Image-Based Dietary Assessment [47]

Issue 4 - Intravenous Glucose Monitoring [48]

Issue 5 - Implanted Glucose Sensors [49]

Issue 6 - AP Using Non-Glucose Data in the Control Algorithm [50]

Related Research Articles

<span class="mw-page-title-main">Hypoglycemia</span> Health condition

Hypoglycemia, also called low blood sugar, is a fall in blood sugar to levels below normal, typically below 70 mg/dL (3.9 mmol/L). Whipple's triad is used to properly identify hypoglycemic episodes. It is defined as blood glucose below 70 mg/dL (3.9 mmol/L), symptoms associated with hypoglycemia, and resolution of symptoms when blood sugar returns to normal. Hypoglycemia may result in headache, tiredness, clumsiness, trouble talking, confusion, fast heart rate, sweating, shakiness, nervousness, hunger, loss of consciousness, seizures, or death. Symptoms typically come on quickly.

<span class="mw-page-title-main">Insulin</span> Peptide hormone

Insulin is a peptide hormone produced by beta cells of the pancreatic islets encoded in humans by the INS gene. It is considered to be the main anabolic hormone of the body. It regulates the metabolism of carbohydrates, fats and protein by promoting the absorption of glucose from the blood into liver, fat and skeletal muscle cells. In these tissues the absorbed glucose is converted into either glycogen via glycogenesis or fats (triglycerides) via lipogenesis, or, in the case of the liver, into both. Glucose production and secretion by the liver is strongly inhibited by high concentrations of insulin in the blood. Circulating insulin also affects the synthesis of proteins in a wide variety of tissues. It is therefore an anabolic hormone, promoting the conversion of small molecules in the blood into large molecules inside the cells. Low insulin levels in the blood have the opposite effect by promoting widespread catabolism, especially of reserve body fat.

<span class="mw-page-title-main">Insulin pump</span> Medical device to administer insulin

An insulin pump is a medical device used for the administration of insulin in the treatment of diabetes mellitus, also known as continuous subcutaneous insulin therapy. The device configuration may vary depending on design. A traditional pump includes:

<span class="mw-page-title-main">Pancreas</span> Organ of the digestive system and endocrine system of vertebrates

The pancreas is an organ of the digestive system and endocrine system of vertebrates. In humans, it is located in the abdomen behind the stomach and functions as a gland. The pancreas is a mixed or heterocrine gland, i.e. it has both an endocrine and a digestive exocrine function. 99% of the pancreas is exocrine and 1% is endocrine. As an endocrine gland, it functions mostly to regulate blood sugar levels, secreting the hormones insulin, glucagon, somatostatin, and pancreatic polypeptide. As a part of the digestive system, it functions as an exocrine gland secreting pancreatic juice into the duodenum through the pancreatic duct. This juice contains bicarbonate, which neutralizes acid entering the duodenum from the stomach; and digestive enzymes, which break down carbohydrates, proteins, and fats in food entering the duodenum from the stomach.

Beta cells (β-cells) are a type of cell found in pancreatic islets that synthesize and secrete insulin and amylin. Beta cells make up 50–70% of the cells in human islets. In patients with Type 1 diabetes, beta-cell mass and function are diminished, leading to insufficient insulin secretion and hyperglycemia.

<span class="mw-page-title-main">Blood sugar level</span> Concentration of glucose present in the blood (Glycaemia)

Glycaemia, also known as blood sugar level, blood sugar concentration, or blood glucose level is the measure of glucose concentrated in the blood of humans and other animals. Approximately 4 grams of dissolved glucose, a simple sugar, is present in the blood plasma of a 70 kg (154 lb) human at all times. The body tightly regulates blood glucose levels as a part of metabolic homeostasis. Glucose is stored in skeletal muscle and liver cells in the form of glycogen; in fasting individuals, blood glucose is maintained at a constant level at the expense of glycogen stores in the liver and skeletal muscle.

<span class="mw-page-title-main">Alpha cell</span>

Alpha cells(α cells) are endocrine cells that are found in the Islets of Langerhans in the pancreas. Alpha cells secrete the peptide hormone glucagon in order to increase glucose levels in the blood stream.

JDRF is a nonprofit 501(c)(3) organization that funds type 1 diabetes (T1D) research, provides a broad array of community and activist services to the T1D population and actively advocates for regulation favorable to medical research and approval of new and improved treatment modalities. It was initially founded as the JDF, the Juvenile Diabetes Foundation. It later changed its name to the Juvenile Diabetes Research Foundation and is now known as JDRF.

<span class="mw-page-title-main">Type 1 diabetes</span> Form of diabetes mellitus

Type 1 diabetes (T1D), formerly known as juvenile diabetes, is an autoimmune disease that originates when cells that make insulin are destroyed by the immune system. Insulin is a hormone required for the cells to use blood sugar for energy and it helps regulate glucose levels in the bloodstream. Before treatment this results in high blood sugar levels in the body. The common symptoms of this elevated blood sugar are frequent urination, increased thirst, increased hunger, weight loss, and other serious complications. Additional symptoms may include blurry vision, tiredness, and slow wound healing. Symptoms typically develop over a short period of time, often a matter of weeks.

The term diabetes includes several different metabolic disorders that all, if left untreated, result in abnormally high concentration of a sugar called glucose in the blood. Diabetes mellitus type 1 results when the pancreas no longer produces significant amounts of the hormone insulin, usually owing to the autoimmune destruction of the insulin-producing beta cells of the pancreas. Diabetes mellitus type 2, in contrast, is now thought to result from autoimmune attacks on the pancreas and/or insulin resistance. The pancreas of a person with type 2 diabetes may be producing normal or even abnormally large amounts of insulin. Other forms of diabetes mellitus, such as the various forms of maturity onset diabetes of the young, may represent some combination of insufficient insulin production and insulin resistance. Some degree of insulin resistance may also be present in a person with type 1 diabetes.

Pulsatile intravenous insulin therapy, sometimes called metabolic activation therapy or cellular activation therapy, describes in a literal sense the intravenous injection of insulin in pulses versus continuous infusions. Injection of insulin in pulses mimics the physiological secretions of insulin by the pancreas into the portal vein which then drains into the liver. In healthy, non-diabetic individuals, pancreatic secretions of insulin correspond to the intake of food. The pancreas will secrete variable amounts of insulin based upon the amount of food consumed among other factors. Continuous exposure to insulin and glucagon is known to decrease the hormones' metabolic effectiveness on glucose production in humans due to the body developing an increased tolerance to the hormones. Down-regulation at the cellular level may partially explain the decreased action of steady-state levels of insulin, while pulsatile hormone secretion may allow recovery of receptor affinity and numbers for insulin. Intermittent intravenous insulin administration with peaks of insulin concentrations may enhance suppression of gluconeogenesis and reduce hepatic glucose production.

Automated insulin delivery systems are automated systems designed to assist people with insulin-requiring diabetes, by automatically adjusting insulin delivery in response to blood glucose levels. Currently available systems can only deliver a single hormone—insulin. Other systems currently in development aim to improve on current systems by adding one or more additional hormones that can be delivered as needed, providing something closer to the endocrine functionality of the pancreas.

<span class="mw-page-title-main">Blood sugar regulation</span> Hormones regulating blood sugar levels

Blood sugar regulation is the process by which the levels of blood sugar, the common name for glucose dissolved in blood plasma, are maintained by the body within a narrow range.

<span class="mw-page-title-main">Insulin (medication)</span> Use of insulin protein and analogs as medical treatment

As a medication, insulin is any pharmaceutical preparation of the protein hormone insulin that is used to treat high blood glucose. Such conditions include type 1 diabetes, type 2 diabetes, gestational diabetes, and complications of diabetes such as diabetic ketoacidosis and hyperosmolar hyperglycemic states. Insulin is also used along with glucose to treat hyperkalemia. Typically it is given by injection under the skin, but some forms may also be used by injection into a vein or muscle. There are various types of insulin, suitable for various time spans. The types are often all called insulin in the broad sense, although in a more precise sense, insulin is identical to the naturally occurring molecule whereas insulin analogues have slightly different molecules that allow for modified time of action. It is on the World Health Organization's List of Essential Medicines. In 2020, regular human insulin was the 307th most commonly prescribed medication in the United States, with more than 1 million prescriptions.

<span class="mw-page-title-main">Minimed Paradigm</span> Insulin pumps

MiniMed Paradigm is a series of insulin pumps manufactured by Medtronic for patients with diabetes mellitus. The pump operates with a single AA battery and uses a piston-plunger pump to infuse a programmed amount of insulin into the patient through a length of tubing. The Paradigm uses a one-way wireless radio frequency link to receive blood sugar measurements from select glucose meters. The Paradigm RT series adds the ability to receive data from a mated continuous blood-glucose monitor. Although the pump can use these measurements to assist in calculating a dose of insulin, no actual change in insulin delivery occurs without manual user-intervention.

Bigfoot Biomedical Inc. is a medical technology start-up headquartered in Milpitas, California, founded by a team of people with personal connections to type 1 and type 2 diabetes.

Boris Petrov Kovatchev is a professor at the University of Virginia where he is the founding Director of the UVA Center for Diabetes Technology, and a principal investigator of the JDRF Artificial Pancreas Project.

The Open Artificial Pancreas System (OpenAPS) project is a free and open-source project that aims to make basic artificial pancreas system (APS) technology available to everyone. The OpenAPS project was designed with the idea of quickly getting the APS technology to more people using a direct approach, rather than waiting for clinical trials to be completed and FDA approval to be granted as is traditional.

<span class="mw-page-title-main">Continuous glucose monitor</span> Blood glucose monitoring device

A continuous glucose monitor (CGM) is a device used for monitoring blood glucose on a continual basis by insulin-requiring people with diabetes, e.g. people with type I, type II diabetes or other types of diabetes. A continuous glucose monitor consists of three parts: a small electrode placed under the skin, a transmitter sending readings at regular intervals, and a separate receiver. Currently approved CGMs use an enzymatic technology which reacts with glucose molecules in the interstitial fluid generating an electric current. This electric current is then relayed from a transmitter attached to the sensor out to a reader which displays the data to the patient.

Gerold Grodsky (1927-2022) was an American professor of biochemistry, biophysics, and medicine at the University of California, San Francisco Diabetes Center, as well as a diabetes researcher. He is most known for his contributions to the modern artificial pancreas.

References

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  2. "Scopus Source List" (Microsoft Excel). Scopus. Elsevier . Retrieved 2014-12-10.
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  4. "Table of Contents — May 2007, 1 (3)". dst.sagepub.com. Retrieved 2016-03-28.
  5. "Table of Contents — July 2007, 1 (4)". dst.sagepub.com. Retrieved 2016-03-28.
  6. "Table of Contents — September 2007, 1 (5)". dst.sagepub.com. Retrieved 2016-03-28.
  7. "Table of Contents — November 2007, 1 (6)". dst.sagepub.com. Retrieved 2016-03-28.
  8. "Table of Contents — January 2008, 2 (1)". dst.sagepub.com. Retrieved 2016-03-28.
  9. "Table of Contents — March 2008, 2 (2)". dst.sagepub.com. Retrieved 2016-03-28.
  10. "Table of Contents — May 2008, 2 (3)". dst.sagepub.com. Retrieved 2016-03-28.
  11. "Table of Contents — July 2008, 2 (4)". dst.sagepub.com. Retrieved 2016-03-28.
  12. "Table of Contents — September 2008, 2 (5)". dst.sagepub.com. Retrieved 2016-03-28.
  13. "Table of Contents — November 2008, 2 (6)". dst.sagepub.com. Retrieved 2016-03-28.
  14. "Table of Contents — March 2009, 3 (2)". dst.sagepub.com. Retrieved 2016-03-28.
  15. "Table of Contents — May 2009, 3 (3)". dst.sagepub.com. Retrieved 2016-03-28.
  16. "Table of Contents — July 2009, 3 (4)". dst.sagepub.com. Retrieved 2016-03-28.
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  29. "Table of Contents — September 2011, 5 (5)". dst.sagepub.com. Retrieved 2016-03-28.
  30. "Table of Contents — November 2011, 5 (6)". dst.sagepub.com. Retrieved 2016-03-28.
  31. "Table of Contents — January 2012, 6 (1)". dst.sagepub.com. Retrieved 2016-03-28.
  32. "Table of Contents — March 2012, 6 (2)". dst.sagepub.com. Retrieved 2016-03-28.
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  39. "Table of Contents — January 2014, 8 (1)". dst.sagepub.com. Retrieved 2016-03-28.
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  45. "Table of Contents — January 2015, 9 (1)". dst.sagepub.com. Retrieved 2016-03-28.
  46. "Table of Contents — March 2015, 9 (2)". dst.sagepub.com. Retrieved 2016-03-28.
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