Is lower and lower better and better? A re-evaluation of the evidence from the Cholesterol Treatment Trialists' Collaboration meta-analysis for low-density lipoprotein Lowering

被引:46
作者
Sniderman, Allan [1 ]
Thanassoulis, George [2 ]
Couture, Patrick [3 ]
Williams, Ken [4 ,5 ]
Alam, Ahsan [6 ]
Furberg, Curt D. [7 ]
机构
[1] McGill Univ, Ctr Hlth, Royal Victoria Hosp, Mike Rosenbloom Lab Cardiovascular Res, Montreal, PQ H3A 1A1, Canada
[2] McGill Univ, Ctr Hlth, Royal Victoria Hosp, Dept Med,Cardiol Div, Montreal, PQ, Canada
[3] Univ Laval, Med Ctr, Lipid Res Ctr, Quebec City, PQ, Canada
[4] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA
[5] KenAnCo Biostat, San Antonio, TX 78229 USA
[6] McGill Univ, Royal Victoria Hosp, Ctr Hlth, Dept Med,Nephrol Div, Montreal, PQ H3A 1A1, Canada
[7] Wake Forest Sch Med, Div Publ Hlth Sci, Winston Salem, NC USA
关键词
Cardiovascular disease; Guidelines; Low-density lipoprotein cholesterol; Prevention; Therapy; HIGH-DOSE ATORVASTATIN; APOLIPOPROTEIN-B; SECONDARY PREVENTION; STATIN THERAPY; RISK; SIMVASTATIN; MANAGEMENT; REDUCTION; TARGETS; EVENTS;
D O I
10.1016/j.jacl.2012.05.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Researchers from the Cholesterol Treatment Trialists' (CTT) Collaboration have argued for maximal lowering of low-density lipoprotein cholesterol (LDL-C) by the use of pharmacologic agents, with the strongest evidence coming from the five comparison statin studies in their second meta-analysis. The CTT meta-analysis has many strengths but also a number of limitations, which have not been discussed and which, given the clinical implications, require consideration. Among these are: (1) the impact and validity of including revascularizations within a composite primary end point; (2) the inclusion of the A-Z study, whose design does not allow for valid comparisons of two statin regimens; (3) the fact that baseline LDL-C levels in the comparison studies were not low enough to test whether statin therapy reduces risk significantly in groups with an initial low LDL-C; and, most important, (4) authors of the five studies compared doses at the extremes of stain regimens. However, the clinical choice is not between the lowest and the greatest dose of a statin stain regimens, for example, between 10 and 80 mg atorvastatin, but, more realistically, between intermediate and high dose, that is, between 40 and 80 mg atorvastatin. On the basis of the CTT meta-analysis, we calculate that any potential gain from increasing the close from 40 to 80 mg atorvastatin would be very small, at best a further 2% further reduction in clinical events. The increase in dose, unfortunately, would likely be associated with increased side effects and decreased compliance. Accordingly, whether net benefit would be demonstrable cannot be assumed. It follows that definitive evidence supporting maximal lowering of LDL-C or maximal close of statins is still lacking and guidelines, if they are to be evidence-based, should acknowledge this uncertainty. (C) 2012 National Lipid Association. All rights reserved.
引用
收藏
页码:303 / 309
页数:7
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