Cardiovascular Disease
Top Cited Papers
- 3 July 2003
- journal article
- review article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 349 (1) , 60-72
- https://doi.org/10.1056/nejmra035098
Abstract
Cardiovascular disease, including stroke, is the leading cause of illness and death in the United States. There are an estimated 62 million people with cardiovascular disease and 50 million people with hypertension in this country.1 In 2000, approximately 946,000 deaths were attributable to cardiovascular disease, accounting for 39 percent of all deaths in the United States.2 Epidemiologic studies and randomized clinical trials have provided compelling evidence that coronary heart disease is largely preventable.3 However, there is also reason to believe that there is a heritable component to the disease. In this review, I highlight what we know now about genetic factors in cardiovascular disease. As future genomic discoveries are translated to the care of patients with cardiovascular disease, it is likely that what we can do will change.Keywords
This publication has 88 references indexed in Scilit:
- Major Outcomes in High-Risk Hypertensive Patients Randomized to Angiotensin-Converting Enzyme Inhibitor or Calcium Channel Blocker vs Diuretic: The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT)JAMA, 2002
- The Effect of Common Polymorphisms of the β2-Adrenergic Receptor on Agonist-Mediated Vascular DesensitizationNew England Journal of Medicine, 2001
- Human Hypertension Caused by Mutations in WNK KinasesScience, 2001
- Transcriptome Analysis Reveals a Role of Interferon-γ in Human Neointima FormationMolecular Cell, 2001
- β 2 -Adrenoceptor Polymorphism Determines Vascular Reactivity in HumansHypertension, 2000
- AT 1 Receptor A/C 1166 Polymorphism Contributes to Cardiac Hypertrophy in Subjects With Hypertrophic CardiomyopathyHypertension, 1998
- The Influence of the Angiotensin I Converting Enzyme Genotype in Familial Hypertrophic Cardiomyopathy Varies with the Disease Gene MutationJournal of Molecular and Cellular Cardiology, 1997
- Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporterNature Genetics, 1996
- Congenitally defective aldosterone biosynthesis in humans: The involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patientsBiochemical and Biophysical Research Communications, 1992
- A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutationPublished by Elsevier ,1990