The role of fibrates in the prevention of cardiovascular disease-a pooled meta-analysis of long-term randomized placebo-controlled clinical trials

被引:94
作者
Saha, Sandeep Ajoy
Kizhakepunnur, Lenney G.
Bahekar, Amol
Arora, Rohit R.
机构
[1] Chicago Med Sch, Div Cardiol, Dept Med, N Chicago, IL 60064 USA
[2] N Chichgo VA Med Ctr, N Chicago, IL 60064 USA
关键词
D O I
10.1016/j.ahj.2007.07.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Fibrates are effective antilipidemic agents with peroxisome proliferator-activated receptor agonist activity, but clinical trial data on their role in cardiovascular prevention are conflicting. We conducted a systematic review and meta-analysis of randomized clinical trials to evaluate their role in prevention of cardiovascular events. Methods A total of 36 489 patients from 10 published randomized placebo-controlled trials were analyzed using the Mantel-Haenszel fixed-effects model. Odds ratios were computed for cardiovascular outcomes from data pooled from the selected trials, and statistical significance was tested using the z-test statistic (2-sided a error <.05). Results Fibrates significantly reduced plasma total cholesterol and triglyceride levels by about 8% and 30%, respectively, and raised high-density lipoprotein cholesterol levels by about 9% compared with placebo. The odds of all-cause mortality tended to be higher (P =.08), and the odds of noncardiovascular mortality were significantly higher (P =.004) with the use of fibrates. However, these significant differences did not persist after exclusion of trials using clofibrate as the study drug. Fibrates did not significantly reduce the odds of cardiovascular mortality (P =.68), fatal myocardial infarction (MI) (P =.76), or stroke (P =.56). On the other hand, fibrates significantly reduced the odds of nonfatal MI by about 22% (P <.00001). The odds of developing cancer were not significantly higher with the use of fibrates (P =.98), nor were the odds of cancer-related death (P =.17). Conclusions In conclusion, our meta-analysis revealed that the long-term use of fibrates significantly reduces the occurrence of nonfatal MI but has no significant effect on other adverse cardiovascular outcomes.
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页码:943 / 953
页数:11
相关论文
共 56 条
[11]   PPAR-α and PPAR-γ activators induce cholesterol removal from human macrophage foam cells through stimulation of the ABCA1 pathway [J].
Chinetti, G ;
Lestavel, S ;
Bocher, V ;
Remaley, AT ;
Neve, B ;
Torra, IP ;
Teissier, E ;
Minnich, A ;
Jaye, M ;
Duverger, N ;
Brewer, HB ;
Fruchart, JC ;
Clavey, V ;
Staels, B .
NATURE MEDICINE, 2001, 7 (01) :53-58
[12]   Primary prevention of cardiovascular disease with atorvastatin in type 2 diabetes in the Collaborative Atorvastatin Diabetes Study (CARDS): multicentre randomised placebo-controlled trial [J].
Colhoun, HM ;
Betteridge, DJ ;
Durrington, PN ;
Hitman, GA ;
Neil, HAW ;
Livingstone, SJ ;
Thomason, MJ ;
Mackness, MI ;
Charlton-Menys, V ;
Fuller, JH .
LANCET, 2004, 364 (9435) :685-696
[13]   Peroxisome proliferator-activated receptor activators inhibit thrombin-induced endothelin-1 production in human vascular endothelial cells by inhibiting the activator protein-1 signaling pathway [J].
Delerive, P ;
Martin-Nizard, F ;
Chinetti, G ;
Trottein, F ;
Fruchart, JC ;
Najib, J ;
Duriez, P ;
Staels, B .
CIRCULATION RESEARCH, 1999, 85 (05) :394-402
[14]   Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels - Results of AFCAPS/TexCAPS [J].
Downs, JR ;
Clearfield, M ;
Weis, S ;
Whitney, E ;
Shapiro, DR ;
Beere, PA ;
Langendorfer, A ;
Stein, EA ;
Kruyer, W ;
Gotto, AM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (20) :1615-1622
[15]   Cardiovascular outcomes in type 2 diabetes - A double-blind placebo-controlled study of bezafibrate: the St. Mary's, Ealing, Northwick Park Diabetes Cardiovascular Disease Prevention (SENDCAP) Study [J].
Elkeles, RS ;
Diamond, JR ;
Poulter, C ;
Dhanjil, S ;
Nicolaides, AN ;
Mahmood, S ;
Richmond, W ;
Mather, H ;
Sharp, P ;
Feher, MD .
DIABETES CARE, 1998, 21 (04) :641-648
[16]   Angiographic assessment of effects of bezafibrate on progression of coronary artery disease in young male postinfarction patients [J].
Ericsson, CG ;
Hamsten, A ;
Nilsson, J ;
Grip, L ;
Svane, B ;
deFaire, U .
LANCET, 1996, 347 (9005) :849-853
[17]  
Frick MH, 1997, CIRCULATION, V96, P2137
[18]   HELSINKI HEART-STUDY - PRIMARY-PREVENTION TRIAL WITH GEMFIBROZIL IN MIDDLE-AGED MEN WITH DYSLIPIDEMIA - SAFETY OF TREATMENT, CHANGES IN RISK-FACTORS, AND INCIDENCE OF CORONARY HEART-DISEASE [J].
FRICK, MH ;
ELO, O ;
HAAPA, K ;
HEINONEN, OP ;
HEINSALMI, P ;
HELO, P ;
HUTTUNEN, JK ;
KAITANIEMI, P ;
KOSKINEN, P ;
MANNINEN, V ;
MAENPAA, H ;
MALKONEN, M ;
MANTTARI, M ;
NOROLA, S ;
PASTERNACK, A ;
PIKKARAINEN, J ;
ROMO, M ;
SJOBLOM, T ;
NIKKILA, EA .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (20) :1237-1245
[19]   Peroxisome proliferator-activated receptor-alpha activators regulate genes governing lipoprotein metabolism, vascular inflammation and atherosclerosis [J].
Fruchart, JC ;
Duriez, P ;
Staels, B .
CURRENT OPINION IN LIPIDOLOGY, 1999, 10 (03) :245-257
[20]   Regulation of lipid and lipoprotein metabolism by PPAR activators [J].
Gervois, P ;
Torra, IP ;
Fruchart, JC ;
Staels, B .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2000, 38 (01) :3-11