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Efficacy and Safety of Pitavastatin in Children and Adolescents with Familial Hypercholesterolemia in Japan and Europe

机译:匹伐他汀在日本和欧洲的家族性高胆固醇血症儿童和青少年中的疗效和安全性

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摘要

>Aim: Children with Familial Hypercholesterolemia (FH) are widely prescribed statins, and it has been suggested that the effects of statins differ among ethnicities. We compared the efficacy and safety of pitavastatin in children and adolescents with FH in clinical trials conducted in Japan and Europe.>Methods: Low-density lipoprotein cholesterol (LDL-C) reductions, adjusted for confounding factors, and safety were compared between the studies in Japan and Europe. In the Japanese study, 14 males with heterozygous FH, aged 11.8 ± 1.6 years, were randomized to 52-week double-blind treatment with 1 or 2 mg/day pitavastatin. In the European study, 106 children and adolescents with high risk hyperlipidemia (103 heterozygous FH), aged 10.6 ± 2.9 years, were randomized to 12-week double-blind treatment with 1, 2 or 4 mg/day pitavastatin or placebo; 84 of these patients and 29 new patients participated in a 52-week open-label extension study.>Results: Age, body weight and baseline LDL-C were identified as factors influencing LDL-C reduction. There were no significant differences in the adjusted mean percentage reduction in LDL-C in Japanese and European children by pitavastatin (24.5% and 23.6%, respectively at 1 mg/day and 33.5% and 30.8%, respectively at 2 mg/day). Pitavastatin was well tolerated without any difference in the frequency or nature of adverse events between the treatment groups, or between the studies.>Conclusion: There were no significant differences between the efficacy or safety of pitavastatin in Japanese and European children and adolescents with FH, suggesting no relevant ethnic differences in the safety or efficacy of pitavastatin.
机译:>目的:家族性高胆固醇血症(FH)的儿童是广泛使用的他汀类药物,并且有人建议他汀类药物的作用因种族而异。我们在日本和欧洲进行的临床试验中比较了匹伐他汀对FH儿童和青少年的疗效和安全性。>方法:针对混杂因素进行调整的低密度脂蛋白胆固醇(LDL-C)降低,以及在日本和欧洲的研究之间比较了安全性。在日本的研究中,将14名11.8±1.6岁的杂合子FH男性随机分为接受1或2 mg /天匹伐他汀治疗的52周双盲治疗。在欧洲的一项研究中,将106名年龄在10.6±2.9岁的高危高脂血症(103杂合子FH)的儿童和青少年随机分为12周的双盲治疗,每天服用1、2或4 mg匹伐他汀或安慰剂。其中84位患者和29位新患者参加了为期52周的开放标签扩展研究。>结果:年龄,体重和基线LDL-C被确定为影响LDL-C降低的因素。匹伐他汀对日本和欧洲儿童的LDL-C调整后平均降低百分比无显着差异(1 mg /天分别为24.5%和23.6%,2 mg /天分别为33.5%和30.8%)。匹伐他汀的耐受性良好,治疗组之间或研究之间不良事件的发生频率或性质没有任何差异。>结论:在日本和欧洲,匹伐他汀的疗效或安全性无显着差异患有FH的儿童和青少年,表明匹伐他汀的安全性或有效性无相关种族差异。

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