4.4 Review

Should both HDL-C and LDL-C be targets for lipid therapy? A review of current evidence

期刊

JOURNAL OF CLINICAL LIPIDOLOGY
卷 1, 期 1, 页码 88-94

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacl.2007.02.004

关键词

Atherosclerosis; Fenofibrate; HDL-cholesterol; Heart disease prevention; Niacin; Torcetrapib

资金

  1. NHLBI NIH HHS [U01 HL081616, P01 HL030086, R01 HL063895] Funding Source: Medline
  2. NIDDK NIH HHS [P30 DK017047, P30 DK035816] Funding Source: Medline
  3. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [P01HL030086, U01HL081616, R01HL063895] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK017047, P30DK035816] Funding Source: NIH RePORTER

向作者/读者索取更多资源

The current guidelines for treatment of high-risk of lipid disorders do not specify a therapeutic target level of high-density lipoprotein cholesterol (HDL-C) for prevention of vascular disease in high-risk populations. However, there is a substantial body of evidence from basic science and epidemiologic studies and from clinical trials, providing the strong, consistent message that raising HDL-C by therapeutic means will effectively and independently reduce cardiovascular risk. This review summarizes epidemiologic evidence and the results of a meta-analysis of 23 published, prospective, randomized, placebo-controlled clinical trials. It focuses on the effects of lipid therapies on coronary stenosis progression, as measured by quantitative arteriography and/or, on clinical cardiovascular endpoints. Among the seven drug/treatment classes into which individual study results were categorized and averaged, reduction in stenosis progression and reduction in clinical events are both very highly correlated with the composite lipid variable (%Delta HDL-C - %Delta low-density lipoprotein cholesterol [LDL-C]; where %Delta is percent change relative to the placebo group response). This holds true for all lipid drug classes or combinations of lipid drug therapy, with the exception of the unexpectedly anomalous effects of the torcetrapib-atorvastatin combination. There is a strong and consistent body of evidence that therapeutic HDL-C-raising is at least as effective as comparable percentages of LDL-C-lowering for reduction of atherosclerosis progression or clinical cardiovascular events over a broad range of risk levels. Adoption of this strategy into guidelines probably awaits results of at least one large controlled HDL-C-raising clinical trial, of which two are ongoing and one other is planned. (C) 2007 National Lipid Association. All fights reserved.

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