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为评价普罗布考调脂作用,将72例原发性高脂血症者随机分为2组,每组36例,P组服普罗布考(Probucol)1.0g/d;F组服非诺贝特(Fenofibrate)0.3g/d,疗程均为3个月。治疗结束时P组和F组服药前后比较,血清总蛋固醇(TC)降低371%和273%,低密度脂蛋白胆固醇(LDLC)降低394%和326%,甘油三酯降低175%和486%,高密度脂蛋白胆固醇(HDLC)P组降低280%,F组升高197%,F组降低脂蛋白(a)193%。结果表明,P组调脂作用TC,LDLC优于F组,TG及HDLC逊于F组。两组副反应情况类似,但P组程度较轻
In order to evaluate the effect of probucol on lipid-lowering, 72 patients with primary hyperlipidemia were randomly divided into two groups, 36 cases in each group, P group received Probucol 1.0g / d, F group Fenofibrate 0.3g / d, treatment are 3 months. At the end of treatment, serum total cholesterol (TC) decreased 371% and 273%, LDLC decreased 394% and 32, respectively 6%, triglycerides decreased by 175% and 486%, HDLC decreased by 280% in P group, 197% in F group, decreased lipoprotein in group F (A) 193%. The results showed that the lipid-lowering effect of P group TC, LDL C better than the F group, TG and HDL C inferior to the F group. The side effects were similar in both groups, but the P group was less severe