Adrenergic Signaling Polymorphisms and Their Impact on Cardiovascular Disease

被引:74
作者
Dorn, Gerald W., II [1 ]
机构
[1] Washington Univ, Sch Med, Dept Internal Med, Ctr Pharmacogenom, St Louis, MO 63110 USA
关键词
BETA(2)-ADRENERGIC RECEPTOR GENE; GENOME-WIDE ASSOCIATION; VASCULAR SMOOTH-MUSCLE; SINGLE-NUCLEOTIDE POLYMORPHISMS; VENTRICULAR EJECTION FRACTION; CARDIAC MYOCYTE APOPTOSIS; CONGESTIVE-HEART-FAILURE; BLOOD-PRESSURE RESPONSE; BETA-BLOCKER-THERAPY; G-PROTEIN;
D O I
10.1152/physrev.00001.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Dorn GW II. Adrenergic Signaling Polymorphisms and Their Impact on Cardiovascular Disease. Physiol Rev 90: 1013-1062, 2010; doi:10.1152/physrev.00001.2010.-This review examines the impact of recent discoveries defining personal genetics of adrenergic signaling polymorphisms on scientific discovery and medical practice related to cardiovascular diseases. The adrenergic system is the major regulator of minute-by-minute cardiovascular function. Inhibition of adrenergic signaling with pharmacological beta-adrenergic receptor antagonists (beta-blockers) is first-line therapy for heart failure and hypertension. Advances in pharmacology, molecular biology, and genetics of adrenergic signaling pathways have brought us to the point where personal genetic differences in adrenergic signaling factors are being assessed as determinants of risk or progression of cardiovascular disease. For a few polymorphisms, functional data generated in cell-based systems, genetic mouse models, and pharmacological provocation of human subjects are concordant with population studies that suggest altered risk of cardiovascular disease or therapeutic response to beta-blockers. For the majority of adrenergic pathway polymorphisms however, published data conflict, and the clinical relevance of individual genotyping remains uncertain. Here, the current state of laboratory and clinical evidence that adrenergic pathway polymorphisms can affect cardiovascular pathophysiology is comprehensively reviewed and compared, with a goal of placing these data in the broad context of potential clinical applicability.
引用
收藏
页码:1013 / 1062
页数:50
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