The Evolution and Refinement of Traditional Risk Factors for Cardiovascular Disease

被引:66
作者
deGoma, Emil M. [1 ]
Knowles, Joshua W. [2 ]
Angeli, Fabio [3 ]
Budoff, Matthew J. [4 ]
Rader, Daniel J. [5 ]
机构
[1] Univ Penn, Div Cardiovasc Med, Philadelphia, PA 19104 USA
[2] Stanford Univ, Med Ctr, Div Cardiovasc Med, Palo Alto, CA 94304 USA
[3] Hosp Media Valle del Tevere, Sect Cardiac Rehabil, Perugia, Italy
[4] Los Angeles Biomed Res Inst, Div Cardiovasc Med, Los Angeles, CA USA
[5] Univ Penn, Div Translat Med & Human Genet, Philadelphia, PA 19104 USA
关键词
prevention; cholesterol; lipoproteins; blood pressure; cardiovascular risk; coronary artery calcium; carotid intima-media thickness; GENOME-WIDE ASSOCIATION; AMBULATORY BLOOD-PRESSURE; CORONARY-HEART-DISEASE; DENSITY-LIPOPROTEIN CHOLESTEROL; ANGIOTENSIN-CONVERTING-ENZYME; CENTRAL AORTIC PRESSURE; 10-YEAR FOLLOW-UP; APOLIPOPROTEIN-B; ARTERY-DISEASE; MASKED HYPERTENSION;
D O I
10.1097/CRD.0b013e318239b924
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Traditional risk factors for cardiovascular disease such as systemic hypertension and hypercholesterolemia, all described more than half a century ago, are relatively few in number. Efforts to expand the epidemiologic canon have met with limited success because of the high hurdle of causality. Fortunately, another solution to current deficiencies in risk assessment-in particular, the underestimation of risk both before and after initiation of pharmacotherapy-may exist. Parallel to the investigation of novel biomarkers, such as high-sensitivity C-reactive protein, ongoing research has yielded improved metrics of known causative conditions. This evolution of traditional risk factors, heralded by measures such as ambulatory blood pressure, central hemodynamics, low density lipoprotein particle concentration, genetic testing, and "vascular age," may better address the detection gap in cardiovascular disease.
引用
收藏
页码:118 / 129
页数:12
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