![]() | This article is an autobiography or has been extensively edited by the subject or by someone connected to the subject.(May 2018) |
Robert Roberts | |
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Born | 9 July 1940 Grole, Newfoundland, Canada |
Education | |
Medical career | |
Profession | physician, academic and medical researcher |
Field | |
Institutions | |
Research | molecular cardiology |
Website | https://drrobertroberts.wordpress.com/ |
Robert Roberts (born 9 July 1940 [1] in Grole, Newfoundland, Canada), is a cardiologist, geneticist, academic, and medical researcher.
Roberts completed his undergraduate at Memorial University of Newfoundland. He attended medical school at Dalhousie University and training in cardiology at University of Toronto in Canada. With a scholarship from the Canadian Heart Foundation he relocated to the U.S. to complete a research fellowship at the University of California-San Diego under the mentorship of Eugene Braunwald and Burton Sobel where he contributed to the clinical trial development of TPA, a first-line treatment for heart attacks. He then became Director of the Coronary Care Unit Barnes Hospital at Washington University in St. Louis (1972–1982) and was recruited by Michael DeBakey and Anthony Gotto to serve as Chief of Cardiology at Baylor College of Medicine in Houston, Texas (1982–2004), which he held for over two decades being one of the longest serving chiefs of cardiology in the US. In 2004, he returned to Canada to become C.E.O., President and Chief Scientific Officer of the University of Ottawa Heart Institute. (2004–2014).
Roberts is currently the chief executive officer of RDS Inc., executive director of the Heart and Vascular Institute and Director of Cardiovascular Genetics and Genomics at Dignity Health at St Joseph's Hospital & Medical Center, Chair of the International Society of Cardiovascular Translational Research at the University of Arizona College of Medicine, and a Professor of Medicine at the University of Arizona College of Medicine. [2]
He served as co-editor of Hurst's The Heart for 25 years, which is the leading practitioner textbook for cardiologists while also being a member of numerous editorial boards for several journals including the current Editor-in-Chief of Current Opinion in Cardiology. [3] For his research contributions, he has received many awards including the Distinguished Scientist of American College of Cardiology and election to the Academy of Scientists of the Royal Society of Canada. As of January 1, 2021, he has over 46,000 citations and a h-index of 105 on Google Scholar.
He was Director of the Coronary Care Unit at Barnes Hospital at Washington University in St. Louis from 1972 to 1982. He served as Chief of Cardiology at Baylor College of Medicine in Houston, Texas from 1982 to 2004, followed by President of the University of Ottawa Heart Institute, Ottawa, Canada, from 2004 to 2014.
Roberts conducted early research in the field of molecular cardiology on the genetic causes of heart disease. [4] [5]
His research is noted for developing the first quantitative assay for MBCK, which was the standard for diagnosing heart attacks in patients for more than three decades and continues to be used in many countries. [6] Most of his research career was devoted to genetics and molecular biology of cardiovascular disorders which led him to several important discoveries, including the mapping of the first gene for atrial fibrillation (1997), the first gene for Wolff-Parkinson-White Syndrome (2001) and many others. His 1998 study on arrhythmogenic right ventricular dysplasia (ARVD) among the population of Grand Falls, Newfoundland and Labrador, Canada, led to the infamous Texas Vampires incident and resulted in a five-year suspension from clinical research by Baylor's Institutional Review Board. [7]
His research is noted for developing the first quantitative assay for MBCK, which was the standard for diagnosing heart attacks in patients for more than three decades. [8] Most of his research career was devoted to genetics and molecular biology of cardiovascular disorders [9] [10] which led him to several important discoveries, including the first gene for atrial fibrillation in 1997, the first gene for Wolff–Parkinson–White syndrome and many others. In 2007, he discovered the first gene for heart attacks (9p21) and since as part of an International Consortium has identified over 100 genetic factors that cause an elevated risk for heart disease in addition to the already commonly associated environmental factors such as cholesterol and smoking. [11] [12] [13] [14]
In 1998, Robert Roberts led a group of researchers from Baylor College of Medicine to conduct a study on arrhythmogenic right ventricular dysplasia (ARVD) among Grand Falls, Newfoundland and Labrador, Canada populations. The group arrived at Grand Falls to collect blood samples from community members to test for biomarkers indicating genetic predispositions of this condition. [15] The study was extremely problematic due to procedures used by Roberts to procure the samples causing significant concerns about the informed consent process of the study. Evidence from an investigation initiated by Baylor's Institutional Review Board found that the consent process was largely skipped or done through medical intimidation by Roberts and his team. Participants also were not given results of the study despite many feeling that they might have died had they not taken part. [16]
Following an internal investigation of this incident by Baylor's Institutional Review Board, Roberts was among three Baylor physicians suspended from clinical research for five years. The study also initiated a special subcommittee investigation of procedural and ethical aspects of the study led by Baylor's IRB and Ottawa Heart Institute which found protocol concerns "of a serious nature". [15]
Roberts has authored over 900 publications in leading scientific journals and received several awards in recognition of his scientific contributions including the Distinguished Scientist Award from the American College of Cardiology (1998), McLaughlin Medal from the Royal Society of Canada (2008), Award of Meritorious Achievement from AHA (2001), Best of What's New by Popular Science (1994), and was elected to Fellow of the Academy of Science of the Royal Society of Canada (2013). [17]
Cardiology is the study of the heart. Cardiology is a branch of medicine that deals with disorders of the heart and the cardiovascular system. The field includes medical diagnosis and treatment of congenital heart defects, coronary artery disease, heart failure, valvular heart disease, and electrophysiology. Physicians who specialize in this field of medicine are called cardiologists, a specialty of internal medicine. Pediatric cardiologists are pediatricians who specialize in cardiology. Physicians who specialize in cardiac surgery are called cardiothoracic surgeons or cardiac surgeons, a specialty of general surgery.
Cardiomyopathy is a group of primary diseases of the heart muscle. Early on there may be few or no symptoms. As the disease worsens, shortness of breath, feeling tired, and swelling of the legs may occur, due to the onset of heart failure. An irregular heart beat and fainting may occur. Those affected are at an increased risk of sudden cardiac death.
Arrhythmogenic cardiomyopathy (ACM), arrhythmogenic right ventricular dysplasia (ARVD), or arrhythmogenic right ventricular cardiomyopathy (ARVC), most commonly is an inherited heart disease.
Short QT syndrome (SQT) is a very rare genetic disease of the electrical system of the heart, and is associated with an increased risk of abnormal heart rhythms and sudden cardiac death. The syndrome gets its name from a characteristic feature seen on an electrocardiogram (ECG) – a shortening of the QT interval. It is caused by mutations in genes encoding ion channels that shorten the cardiac action potential, and appears to be inherited in an autosomal dominant pattern. The condition is diagnosed using a 12-lead ECG. Short QT syndrome can be treated using an implantable cardioverter-defibrillator or medications including quinidine. Short QT syndrome was first described in 2000, and the first genetic mutation associated with the condition was identified in 2004.
The University of Ottawa Heart Institute (UOHI) (French: Institut de cardiologie de l'Université d'Ottawa ) is Canada's largest cardiovascular health centre. It is located in Ottawa, Ontario, Canada. It began as a department in The Ottawa Hospital, and since has evolved into Canada's only complete cardiac centre, encompassing prevention, diagnosis, treatment, rehabilitation, research, and education.
Plakoglobin, also known as junction plakoglobin or gamma-catenin, is a protein that in humans is encoded by the JUP gene. Plakoglobin is a member of the catenin protein family and homologous to β-catenin. Plakoglobin is a cytoplasmic component of desmosomes and adherens junctions structures located within intercalated discs of cardiac muscle that function to anchor sarcomeres and join adjacent cells in cardiac muscle. Mutations in plakoglobin are associated with arrhythmogenic right ventricular dysplasia.
Ryanodine receptor 2 (RYR2) is one of a class of ryanodine receptors and a protein found primarily in cardiac muscle. In humans, it is encoded by the RYR2 gene. In the process of cardiac calcium-induced calcium release, RYR2 is the major mediator for sarcoplasmic release of stored calcium ions.
The following outline is provided as an overview of and topical guide to cardiology, the branch of medicine dealing with disorders of the human heart. The field includes medical diagnosis and treatment of congenital heart defects, coronary artery disease, heart failure, valvular heart disease and electrophysiology. Physicians who specialize in cardiology are called cardiologists.
Desmocollin-2 is a protein that in humans is encoded by the DSC2 gene. Desmocollin-2 is a cadherin-type protein that functions to link adjacent cells together in specialized regions known as desmosomes. Desmocollin-2 is widely expressed, and is the only desmocollin isoform expressed in cardiac muscle, where it localizes to intercalated discs. Mutations in DSC2 have been causally linked to arrhythmogenic right ventricular cardiomyopathy.
Plakophilin-2 is a protein that in humans is encoded by the PKP2 gene. Plakophilin 2 is expressed in skin and cardiac muscle, where it functions to link cadherins to intermediate filaments in the cytoskeleton. In cardiac muscle, plakophilin-2 is found in desmosome structures located within intercalated discs. Mutations in PKP2 have been shown to be causal in arrhythmogenic right ventricular cardiomyopathy.
Landiolol (INN) is an ultra short-acting, β1-superselective intravenous adrenergic antagonist, which decreases the heart rate effectively with less negative effect on blood pressure or myocardial contractility. In comparison to other beta blockers, landiolol has the shortest elimination half-life, ultra-rapid onset of effect, and predictable effectiveness with inactive metabolites. The pure S-enantiomer structure of landiolol is believed to develop less hypotensive side effects in comparison to other β-blockers. This has a positive impact on the treatment of patients when reduction of heart rate without decrease in arterial blood pressure is desired. Landiolol was developed by modifying the chemical structure of esmolol to produce a compound with a higher rate of cardioselectivity and a greater potency without increasing its duration of action. It is sold as landiolol hydrochloride. Based on its positive benefit risk profile, landiolol has been granted the marketing authorization and introduced to the European markets under the brand names Rapibloc, Raploc, Runrapiq, Landibloc mid 2016. Landiolol is available in Japan under the brand names Onoact (50 mg) and Corbeta.
Michel Haïssaguerre is a French cardiologist and electrophysiologist. His investigations have been the basis for development of new markers and therapies for atrial and ventricular fibrillation.
Atrial fibrillation is an abnormal heart rhythm (arrhythmia) characterized by rapid and irregular beating of the atrial chambers of the heart. It often begins as short periods of abnormal beating, which become longer or continuous over time. It may also start as other forms of arrhythmia such as atrial flutter that then transform into AF.
Jonathan L. Halperin is an American cardiologist and the author of Bypass (ISBN 0-89586-509-2), among the most comprehensive works on the subject of coronary artery bypass surgery. In addition, he is the Robert and Harriet Heilbrunn Professor of Medicine at The Mount Sinai School of Medicine as well as Director of Clinical Cardiology in the Zena and Michael A. Wierner Cardiovascular Institute at The Mount Sinai Medical Center, both in New York City. Halperin was the principal cardiologist responsible for both the design and execution of the multi-center Stroke Prevention in Atrial Fibrillation (SPAF) clinical trials, funded by the National Institutes of Health, which helped develop antithrombotic strategies to prevent stroke, and he subsequently directed the SPORTIF clinical trials, which evaluated the first oral direct thrombin inhibitor for prevention of stroke in patients with atrial fibrillation.
Heart rhythm disturbances have been seen among astronauts. Most of these have been related to cardiovascular disease, but it is not clear whether this was due to pre-existing conditions or effects of space flight. It is hoped that advanced screening for coronary disease has greatly mitigated this risk. Other heart rhythm problems, such as atrial fibrillation, can develop over time, necessitating periodic screening of crewmembers’ heart rhythms. Beyond these terrestrial heart risks, some concern exists that prolonged exposure to microgravity may lead to heart rhythm disturbances. Although this has not been observed to date, further surveillance is warranted.
Frank I. Marcus was an American cardiologist and Emeritus Professor of Medicine at the University of Arizona Health Sciences Center, the author of more than 290 publications in peer-reviewed medical journals and of 90 book chapters. He was considered a world expert on arrhythmogenic right ventricular cardiomyopathy (ARVC) and was a member of the Editorial/Scientific Board of 14 Cardiovascular Journals as well as a reviewer for 26 other medical publications.
The Texas Vampires were a name given to a group of researchers from Baylor College of Medicine who in 1998 conducted a study on arrhythmogenic right ventricular dysplasia (ARVD) among the population of Grand Falls-Windsor, Newfoundland and Labrador, Canada. The study team was led by Dr. Robert Roberts (cardiologist), who was president and CEO of the University of Ottawa Heart Institute from 2004 to 2014.
Yaariv Khaykin is a Canadian cardiologist and a clinical researcher in the area of electrophysiology. He is the director of the Newmarket Electrophysiology Research Group at the Southlake Regional Health Centre. He has published research into complex ablation and pioneered cardiac ablation methods.
Tarlochan Singh Kler is an Indian interventional cardiologist, medical administrator, writer, Chairman at Fortis Heart and Vascular Institute, and. Born in Amargarh in the Indian state of Punjab, he graduated in medicine from Punjabi University in 1976, secured his MD in general medicine from Postgraduate Institute of Medical Education and Research (PGIMER) in 1980 and followed it up with the degree of DM in cardiology from the same institution in 1983. He succeeded Naresh Trehan as the executive director of Fortis Heart Institute and Research Centre before becoming its director. He has written several articles on interventional cardiology; Persistent left superior vena cava opening directly into right atrium and mistaken for coronary sinus during biventricular pacemaker implantation, Mammary coronary artery anastomosis without cardiopulmonary bypass through minithoracotomy: one year clinical experience, and Ventricular Fibrillation in the EP Lab. What is the Atrial Rhythm? are some of the notable ones. The Government of India awarded him the third highest civilian honour of the Padma Bhushan, in 2005, for his contributions to medicine.
Günter Breithardt is a German physician, cardiologist and emeritus university professor. He is known for his research in the field of rhythmology, especially the diagnosis and pharmacological and non-pharmacological therapy of cardiac arrhythmias and acute cardiac death, in particular the identification of arrhythmia-triggering gene mutations. For 21 years he headed the Medical Clinic and Polyclinic C at Münster University Hospital. A number of his academic students hold university management and chief physician positions.