Galetta F, Sampietro T, Basta G, Giannasi G, Bionda A
Istituto di Clinica Medica II, Università degli Studi, Pisa.
Minerva Med. 1995 Jul-Aug;86(7-8):299-303.
The efficacy of Simvastatin to reduce plasma cholesterol is well documented. Other molecule within the lipo-lipoprotein family, such as, particularly, lipoprotein (a) -Lp(a)-, have been recently found to have a predictive and/or causative role in atherosclerosis. Based on the above consideration, we studied 20 patients (7 females and 13 males), mean age 52.4 +/- 14.2 years, affected by primary hypercholesterolemia to evaluate the effect of simvastatin on Lp(a), in addition to the classic lipidic parameters. Five weeks after suspension of lipid-lowering drugs and on a normal caloric-fat diet, were given 20 mg simvastatin/day for 12 months. Clinical and laboratory parameters, cholesterol (CH), triglycerides (TG), high density and low density lipoprotein cholesterol (HDL-CH and LDH-CH) measured enzymatically, apoproteins A1, B measured radial immunodiffusion technique and Lp(a) measured as apoprotein(a) with immunoradiometric assay and were evaluated before therapy and after 12 months of therapy. Simvastatin determined a significant reduction in total cholesterol and cholesterol-LDL (CH 327.7 +/- 44.4 vs 255.5 +/- 37.3, p < 0.0001; LDL-CH 257.1 +/- 60.9 vs 183.8 +/- 46.9, p < 0.0001) and a significant increase in HDL-CH (36.7 +/- 5.9 vs 40.2 +/- 5.7, p < 0.005); no variation was observed in triglycerides (TG) levels. Simvastatin therapy further determined a significant increase in Lp(a) plasma levels (43.8 +/- 25.6 vs 50.5 +/- 28.0, p < 0.02). The our data, in agreement with those documenting the beneficial effect of Simvastatin in greatly decreasing CH and LDL-CH, but point out the need for further studies concerning the long-ter effect of simvastatin on Lp(a), in order to fully establish its role in the secondary prevention of atherosclerosis.
辛伐他汀降低血浆胆固醇的疗效已有充分记录。脂蛋白家族中的其他分子,尤其是脂蛋白(a)[Lp(a)],最近被发现在动脉粥样硬化中具有预测和/或致病作用。基于上述考虑,我们研究了20例原发性高胆固醇血症患者(7名女性和13名男性),平均年龄52.4±14.2岁,以评估辛伐他汀除对经典脂质参数的影响外,对Lp(a)的作用。在停用降脂药物并采用正常热量脂肪饮食5周后,给予患者每天20mg辛伐他汀,持续12个月。在治疗前和治疗12个月后,对临床和实验室参数进行评估,包括酶法测定的胆固醇(CH)、甘油三酯(TG)、高密度和低密度脂蛋白胆固醇(HDL-CH和LDL-CH),放射免疫扩散技术测定的载脂蛋白A1、B,免疫放射分析法定量测定的Lp(a)。辛伐他汀使总胆固醇和低密度脂蛋白胆固醇显著降低(CH:327.7±44.4对255.5±37.3,p<0.0001;LDL-CH:257.1±60.9对183.8±46.9,p<0.0001),高密度脂蛋白胆固醇显著升高(36.7±5.9对40.2±5.7,p<0.005);甘油三酯(TG)水平未观察到变化。辛伐他汀治疗还使血浆Lp(a)水平显著升高(43.8±25.6对50.5±28.0,p<0.02)。我们的数据与那些记录辛伐他汀在大幅降低CH和LDL-CH方面有益作用的数据一致,但指出需要进一步研究辛伐他汀对Lp(a)的长期影响,以便全面确定其在动脉粥样硬化二级预防中的作用。