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J Am Coll Cardiol, 2007; 49:2003-2009, doi:10.1016/j.jacc.2007.01.083 (Published online 3 May 2007).
© 2007 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: CORONARY ARTERY DISEASE

Low-Density Lipoprotein-Dependent and -Independent Effects of Cholesterol-Lowering Therapies on C-Reactive Protein

A Meta-Analysis

Scott Kinlay, MBBS, PhD, FRACP, FACC*,1

Veteran’s Affairs Boston Healthcare System, West Roxbury Campus, Brigham and Women’s Hospital, and Harvard Medical School, Boston, Massachusetts.

Manuscript received January 19, 2006; revised manuscript received December 19, 2006, accepted January 3, 2007.

* Reprint requests and correspondence: Dr. Scott Kinlay, Cardiovascular Division, VA Boston Healthcare System, 1400 VFW Parkway, West Roxbury, Massachusetts 02132. (Email: skinlay{at}partners.org).

Objectives: This study sought to assess the contribution of low-density lipoprotein (LDL)–dependent and LDL–independent effects of LDL-lowering therapies to changes in C-reactive protein (CRP) in healthy or stable subjects.

Background: Correlations of change in LDL and CRP in individuals are lowered by their measurement variability. By using average changes in LDL and CRP in study groups, meta-analysis reduces this variability to better assess their correlation.

Methods: A systematic search for randomized placebo-controlled trials reporting change in LDL and CRP with LDL-lowering interventions retrieved 23 studies with 57 groups treated with a variety of statins, nonstatin drugs, or other regimens. Meta-analysis techniques assessed the relationships between average mean differences (placebo – treatment) in change in CRP and LDL.

Results: The overall reduction in CRP was 28% (95% confidence interval 26% to 30%). Significantly greater CRP reduction occurred in statin and statin-ezetimibe interventions, interventions using 80 mg/day of statins, and with greater LDL lowering. Meta-regression analysis showed a strong correlation between the change in LDL and CRP (r = 0.80, p < 0.001). Statin therapies had no significant effect on CRP after adjusting for the change in LDL. In a multivariate model applied to a range of LDL reduction typically seen with statins (20% to 60%), 89% to 98% of CRP change was related to LDL lowering and 2% to 11% was related to non-LDL effects of statins.

Conclusions: In clinical practice, most of the anti-inflammatory effect of LDL-lowering therapies is related to the magnitude of change in LDL. The potential non-LDL effects of statins on inflammation are much smaller in magnitude.

Abbreviations and Acronyms
  CRP = C-reactive protein
  LDL = low-density lipoprotein
  RCT = randomized controlled trial


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