Relation of gemfibrozil treatment and lipid levels with major coronary events - VA-HIT: A randomized controlled trial

Citation
Sj. Robins et al., Relation of gemfibrozil treatment and lipid levels with major coronary events - VA-HIT: A randomized controlled trial, J AM MED A, 285(12), 2001, pp. 1585-1591
Citations number
46
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
ISSN journal
00987484 → ACNP
Volume
285
Issue
12
Year of publication
2001
Pages
1585 - 1591
Database
ISI
SICI code
0098-7484(20010328)285:12<1585:ROGTAL>2.0.ZU;2-O
Abstract
Context A low plasma level of high-density lipoprotein cholesterol (HDL-C) is a major risk factor for coronary heart disease (CHD). A secondary preven tion study, the Veterans Affairs High-Density Lipoprotein Intervention Tria l (VA-HIT), demonstrated that CHD events were significantly reduced during a median follow-up of 5.1 years by treating patients with the fibric acid d erivative gemfibrozil when the predominant lipid abnormality was low HDL-C. Objective To determine if the reduction in major CHD events with gemfibrozi l in VA-HIT could be attributed to changes in major plasma lipid levels. Design Multicenter, randomized, double-blind, placebo-controlled trial cond ucted from September 1991 to August 1998. Setting The Department of Veterans Affairs Cooperative Studies Program, in which 20 VA medical centers were participating sites. Participants A total of 2531 men with a history of CHD who had low HDL-C le vels (mean, 32 mg/dL [0.83 mmol/L] ) and low low-density lipoprotein choles terol (LDL-C) levels (mean, 111 mg/dL [2.88 mmol/L]). Intervention Participants were randomly assigned to receive gemfibrozil, 12 00 mg/d (n =1264), or matching placebo (n = 1267). Main Outcome Measure Relation of lipid levels at baseline and averaged duri ng the first 18 months of gemfibrozil treatment with the combined incidence of nonfatal myocardial infarction and CHD death. Results Concentrations of HDL-C were inversely related to CHD events. Multi variable Cox proportional hazards analysis showed that CHD events were redu ced by 11% with gemfibrozil for every 5-mg/dL (0.13-mmol/L) increase in HDL -C (P = .02). Events were reduced even further with gemfibrozil beyond that explained by increases in HDL-C values, particularly in the second through fourth quintiles of HDL-C values during treatment. During gemfibrozil trea tment, only the increase in HDL-C significantly predicted a lower risk of C HD events; by multivariable analysis, neither triglyceride nor LDL-C levels at baseline or during the trial predicted CHD events. Conclusions Concentrations of HDL-C achieved with gemfibrozil treatment pre dicted a significant reduction in CHD events in patients with low HDL-C lev els, However, the change in HDL-C levels only partially explained the benef icial effect of gemfibrozil.