A comparison of pravastatin and gemfibrozil in the treatment of dyslipoproteinemia in patients with non-insulin-dependent diabetes mellitus

被引:16
|
作者
Schweitzer, M
Tessier, D
Vlahos, WD
Leiter, L
Collet, JP
McQueen, MJ
Harvey, L
Alaupovic, P
机构
[1] Sir Mortimer B Davis Jewish Hosp, Montreal, PQ H3T 1E2, Canada
[2] Univ Sherbrooke, Ctr Hosp, Sherbrooke, PQ, Canada
[3] St Pauls Hosp, Dept Endocrinol & Metab, Vancouver, BC V6Z 1Y6, Canada
[4] St Michaels Hosp, Dept Endocrinol & Metab, Hamilton, ON, Canada
[5] Sir Mortimer B Davis Jewish Hosp, Randomized Clin Trial Unit, Montreal, PQ, Canada
[6] McGill Univ, Dept Epidemiol & Biostat, Montreal, PQ, Canada
[7] Hamilton Gen Hosp, Dept Lab Med, Hamilton, ON, Canada
[8] Bristol Myers Squibb Co, Div Cardiol, Kingston, ON, Canada
[9] Oklahoma Med Res Fdn, Lipid & Lipoprotein Lab, Oklahoma City, OK 73104 USA
关键词
pravastatin; gemfibrozil; hydrox methylglutaryl CoA reductase inhibitor; fibrate; lipoprotein particles; cholesterol; triglycerides;
D O I
10.1016/S0021-9150(01)00700-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effects of pravastatin (pravachol) compared with gemfibrozil on cholesterol-rich and trigy1ceride- rich lipoproteins were evaluated in this multi-centered trial. Following an 8-12 week prerandomization phase, 136 patients with NIDDM and hypercholesterolemia were randomized to receive either pravastatin 40 mg or gemifibrozil 1200 mg daily for 16 weeks. The reduction of total cholesterol (TC), betaquant LDL and LDL cholesterol (LDL-C) was significantly greater in patients treated with pravastatin than with gemfibrozil. However, gemofibrozil treatment resulted in a significantly greater reduction of triglyceride (TG) levels than did treatment with pravastatin. Pravastatin reduced the concentration of apoB (- 19.3%, P < 0.001) and cholesterol-rich Lp-B (Lp-B + Lp-B; E) particles (- 19%, P < 0.001) to a significantly greater extent (P < - 0.001) than gemfibrozil (- 4.1 and - 1%, respectively). Both gemfibrozil and pravastatin reduced the concentrations of triglyceride-rich Lp-Bc (- 12.2 and - 13.3%, respectively) and Lp-A-II;B;C;D;E ( - 19 and - 12.7%, respectively) particles and their characteristic apoC-III constituent (-10.0 and -7.0%, respectively). In contrast, gemfibozil has a greater lowering effect compared with pravastatin on TG levels 29.6 vs. - 6.3%, respectively). Both pravastatin and gemfibrozil significantly increased the levels of apoA-I and, with both drugs, the elevated concentrations of apoA-I were due to significantly increased levels of Lp-A-I:A-II particles. By decreasing both cholesterol-rich Lp-B and triglyceride-rich Lp-Bc particles and increasing HDL-C and Lp-A-LA-II particles in addition to proven efficacy in decreasing coronary events in NIDDNI patients, pravastatin appears to be an appropriate choice for monotherapy in a broad range of diabetic patients with Type IIA and Type IIB hyperlipoproteinemias. These results also showed that direct measurement of lipoprotein family of particles provides important information not only about the composition but also the type and number of apoA- and apoB-containing lipoprotein particles. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:201 / 210
页数:10
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