Beyond LDL-cholesterol reduction: the way ahead in managing dyslipidaemia

被引:12
作者
Chapman, J [1 ]
机构
[1] Hop Pitie, Natl Inst Hlth & Med Res, F-75651 Paris, France
关键词
HDL-cholesterol; atherosclerosis; cardiovascular risk; dyslipidaemia;
D O I
10.1093/eurheartj/sui044
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Observational cohort studies and analysis of the populations of intervention trials at baseline reveal a strong inverse association between circulating levels of high-density lipoprotein (HDL)-cholesterol at baseline and the risk of a fatal or non-fatal cardiovascular event. Intervention with a statin is as effective, in absolute terms, in reducing the risk of coronary events in patients across a wide range of dyslipidaemic phenotypes, including those with low HDL-cholesterol. However, statins exert little effect on the levels of HDL-cholesterol, and treatment with a statin does not eliminate the excess risk associated with low HDL-cholesterol. Additional therapy is clearly required to address this residual risk. The success of clinical evaluations of agents that increase HDL-cholesterol, such as nicotinic acid or fibrate drugs, in reducing the incidence of cardiovascular events points to a way forward. Evidence from outcome studies already points to superior cardiovascular risk reductions in patients receiving a statin plus nicotinic acid, and intensive multi-drug regimens based on such combinations probably represent the way to achieve cardiovascular risk reductions greater than those possible with a statin alone. Accurate and well-validated assays for measuring HDL-cholesterol and more precise definition of optimal levels of HDL-cholesterol in patients with different levels of cardiovascular risk are required. These advances will facilitate the future drafting of guidelines that include correction of low HDL-cholesterol alongside reduction of low-density lipoprotein cholesterol within clinical algorithms for reducing cardiovascular risk.
引用
收藏
页码:F56 / F62
页数:7
相关论文
共 56 条
[21]   Clinical review 124 - Diabetic dyslipidemia: Causes and consequences [J].
Goldberg, IJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (03) :965-971
[22]   Isolated low HDL cholesterol as a risk factor for coronary heart disease mortality - A 21-year follow-up of 8000 men [J].
Goldbourt, U ;
Yaari, S ;
Medalie, JH .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (01) :107-113
[23]   HIGH-DENSITY LIPOPROTEIN AS A PROTECTIVE FACTOR AGAINST CORONARY HEART-DISEASE - FRAMINGHAM STUDY [J].
GORDON, T ;
CASTELLI, WP ;
HJORTLAND, MC ;
KANNEL, WB ;
DAWBER, TR .
AMERICAN JOURNAL OF MEDICINE, 1977, 62 (05) :707-714
[24]   Assessing low levels of high-density lipoprotein cholesterol as a risk factor in coronary heart disease - A working group report and update [J].
Gotto, AM ;
Brinton, EA .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (05) :717-724
[25]   Action of atorvastatin in combined hyperlipidemia - Preferential reduction of cholesteryl ester transfer from HDL to VLDL1 particles [J].
Guerin, M ;
Lassel, TS ;
Le Goff, W ;
Farnier, M ;
Chapman, MJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (01) :189-197
[26]   Dose-dependent action of atorvastatin in type IIB hyperlipidemia: preferential and progressive reduction of atherogenic apoB-containing lipoprotein subclasses (VLDL-2, IDL, small dense LDL) and stimulation of cellular cholesterol efflux [J].
Guerin, M ;
Egger, P ;
Soudant, C ;
Le Goff, W ;
van Tol, A ;
Dupuis, R ;
Chapman, MJ .
ATHEROSCLEROSIS, 2002, 163 (02) :287-296
[27]   Extended-released niacin for modifying the lipoprotein profile [J].
Guyton, JR .
EXPERT OPINION ON PHARMACOTHERAPY, 2004, 5 (06) :1385-1398
[28]   Treatment of hyperlipidemia with combined niacin-statin regimens [J].
Guyton, JR ;
Capuzzi, DM .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 82 (12A) :82U-84U
[29]  
Haffner Steven M, 2004, Diabetes Care, V27 Suppl 1, pS68
[30]   Metabolic syndrome is associated with elevated oxidative stress and dysfunctional dense high-density lipoprotein particles displaying impaired antioxidative activity [J].
Hansel, B ;
Giral, P ;
Nobecourt, E ;
Chantepie, S ;
Bruckert, E ;
Chapman, MJ ;
Kontush, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (10) :4963-4971