Huttunen J K, Frick M H, Heinonen O P, Heinsalmi P, Manninen V, Mänttäri M, Romo M
First Department of Medicine, University of Helsinki, Finland.
Drugs. 1988;36 Suppl 3:32-6. doi: 10.2165/00003495-198800363-00009.
The Helsinki Heart Study tested the effect of modifying plasma low density lipoprotein (LDL)- and high density lipoprotein (HDL)-cholesterol on the primary prevention of coronary heart disease in middle-aged men with non-HDL-cholesterol greater than or equal to 5.2 mmol/L (200 mg/dl). One group (2046 men) received 600mg of gemfibrozil twice daily, and the other (2035 men) received placebo. Averaged over the 5-year trial period, gemfibrozil induced mean decreases of 11% in LDL-cholesterol and 35% in triglycerides and a mean increase of 11% in HDL-cholesterol compared with placebo. These changes were accompanied by a 34% reduction (number of end-points; 56 vs 84) in the incidence of coronary heart disease. The reduction was largest in subjects with type IIB hyperlipoproteinaemia and smallest in subjects with type IIA hyperlipoproteinaemia. The changes in serum HDL- and LDL-cholesterol during the trial were associated (p less than 0.02 and p less than 0.05, respectively) with the risk of coronary heart disease in the gemfibrozil group, but not in the placebo group.
赫尔辛基心脏研究检测了调节血浆低密度脂蛋白(LDL)和高密度脂蛋白(HDL)胆固醇对非HDL胆固醇大于或等于5.2 mmol/L(200 mg/dl)的中年男性冠心病一级预防的效果。一组(2046名男性)每天两次服用600毫克吉非贝齐,另一组(2035名男性)服用安慰剂。在5年的试验期内,与安慰剂相比,吉非贝齐使LDL胆固醇平均降低11%,甘油三酯平均降低35%,HDL胆固醇平均升高11%。这些变化伴随着冠心病发病率降低34%(终点事件数量;56例对84例)。这种降低在IIB型高脂蛋白血症患者中最大,在IIA型高脂蛋白血症患者中最小。在试验期间,吉非贝齐组血清HDL和LDL胆固醇的变化分别与冠心病风险相关(p<0.02和p<0.05),但在安慰剂组中则不然。