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Safety and efficacy of long-term combination therapy with bezafibrate and ezetimibe in patients with dyslipidemia in the prospective, observational J-COMPATIBLE study

机译:一项前瞻性观察性J-相容性研究表明,苯扎贝特和依折麦布长期联合治疗血脂异常的安全性和有效性

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Background There are numerous reports describing the efficacy of fenofibrate in combination with ezetimibe for treating dyslipidemia. In contrast, a study combining bezafibrate and ezetimibe has not yet been conducted. In this study, we examined the safety, including the risk of gallstone formation, and the efficacy of long-term combination therapy with bezafibrate and ezetimibe for treating dyslipidemia. Methods Dyslipidemic patients treated with 400?mg/day bezafibrate in combination with 10?mg/day ezetimibe for the first time were eligible. We selected 157 institutions in Japan and conducted a 12-month prospective observational study, with patients enrolled on the day they started combination therapy. Safety of the combination was examined in terms of the type, onset, and severity of adverse drug reactions (ADRs). Efficacy was evaluated in terms of the changes in low-density lipoprotein-cholesterol (LDL-C), high-density lipoprotein-cholesterol (HDL-C), triglyceride (TG), and non-HDL cholesterol (non-HDL-C) levels from the start of combination therapy (baseline) to the last observation carried forward (LOCF). Lipid levels were assessed at 1, 3, 6, and 12?months after starting combination therapy. Results We enrolled 665 patients in this observational study. Safety was evaluated in 659, and ADRs occurred in 42 patients (6.4%). The most frequent ADRs were blood creatine phosphokinase increase (1.5%) and myalgia (0.8%). Asymptomatic gallstones were observed in four patients (0.6%). Effectiveness was evaluated in 622 patients. LDL-C, HDL-C, TG, and non-HDL-C levels improved significantly from baseline to LOCF by ?17.4%, 8.8%, –40.5%, and ?21.6%, respectively (all, p? Conclusions Bezafibrate in combination with ezetimibe is safe and effective, and is potentially useful for comprehensive management of dyslipidemia.
机译:背景技术有大量报道描述非诺贝特联合依折麦布治疗血脂异常的疗效。相反,尚未进行将苯扎贝特和依泽替米贝联合使用的研究。在这项研究中,我们检查了安全性,包括胆结石形成的风险,以及苯扎贝特和依折麦布长期联合治疗血脂异常的疗效。方法首次将400 mg /天的苯扎贝特联合10 mg /天的依泽替米贝治疗的血脂异常患者纳入研究。我们选择了日本的157家机构,并进行了为期12个月的前瞻性观察性研究,患者在开始联合治疗的当天就入选。根据药物不良反应(ADR)的类型,发作和严重程度检查了该组合的安全性。根据低密度脂蛋白胆固醇(LDL-C),高密度脂蛋白胆固醇(HDL-C),甘油三酸酯(TG)和非HDL胆固醇(non-HDL-C)的变化评估疗效从开始联合治疗(基线)到最后进行的观察值(LOCF)的水平。在开始联合治疗后的1、3、6和12个月时评估血脂水平。结果我们在这项观察性研究中招募了665名患者。在659位患者中评估了安全性,在42位患者中发生了ADR(6.4%)。最常见的ADR是血肌酸磷酸激酶升高(1.5%)和肌痛(0.8%)。在四名患者(0.6%)中观察到无症状的胆结石。评价了622例患者的有效性。从基线到LOCF,LDL-C,HDL-C,TG和非HDL-C的水平分别显着提高了[17.4%],[8.8%],[[40.5%]和​​[21.6%]。依泽替米贝联合用药安全有效,对血脂异常的综合管理有潜在的帮助。

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