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Clinical Applications of a Novel Selective PPARα Modulator Pemafibrate in Dyslipidemia and Metabolic Diseases

机译:新型选择性PPARα调节剂Pemafibrate在血脂异常和代谢性疾病中的临床应用

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摘要

Fasting and postprandial hypertriglyceridemia is a risk factor for atherosclerotic cardiovascular diseases (ASCVD). Fibrates have been used to treat dyslipidemia, particularly hypertriglyceridemia, and low HDL-cholesterol (HDL-C). However, conventional fibrates have low selectivity for peroxisome proliferator-activated receptor (PPAR)α. Fibrates' clinical use causes side effects such as worsening liver function and elevating the creatinine level. Large-scale clinical trials of fibrates have shown negative results for prevention of ASCVD. To overcome these issues, the concept of the selective PPARα modulator (SPPARMα), with a superior balance of efficacy and safety, has been proposed. A SPPARMα, pemafibrate (K-877), was synthesized by Kowa Company, Ltd. for better efficacy and safety. Clinical trials conducted in Japan confirmed the superior effects of pemafibrate on triglyceride reduction and HDL-C elevation.Conventional fibrates showed elevated liver function test values and worsened kidney function test values, while pemafibrate demonstrated improved liver function test values and was less likely to increase serum creatinine or decrease the estimated glomerular filtration rate. There were extremely few drug interactions even when it was used concomitantly with various statins. Furthermore, unlike many of the conventional fibrates that are renal excretory-type drugs, pemafibrate is excreted into the bile, so it can be safely used even in patients with impaired renal function and there is no increase in its blood concentration.This novel SPPARMα, pemafibrate, has superior benefit-risk balance compared to conventional fibrates and can be used for patients for whom it was difficult to use existing fibrates, including those who are taking statins and those with renal dysfunction. A large-scale trial PROMINENT using pemafibrate for patients with type 2 diabetes is in progress. In the current review, the latest data on pemafibrate will be summarized.
机译:空腹和餐后高甘油三酯血症是动脉粥样硬化性心血管疾病(ASCVD)的危险因素。贝特类药物已被用于治疗血脂异常,尤其是高甘油三酯血症和低HDL-胆固醇(HDL-C)。但是,常规贝特类药物对过氧化物酶体增殖物激活受体(PPAR)α的选择性低。贝特类药物的临床使用会引起副作用,例如肝功能恶化和肌酐水平升高。贝特类药物的大规模临床试验已显示出预防ASCVD的阴性结果。为了克服这些问题,已经提出了在功效和安全性之间具有优异平衡的选择性PPARα调节剂(SPPARMα)的概念。为了提高药效和安全性,Kowa Company,Ltd.合成了SPPARMα(多马贝酸盐(K-877))。在日本进行的临床试验证实了贝马贝特对降低甘油三酸酯和HDL-C升高具有优越的作用;常规贝马特表明肝功能测试值升高而肾功能测试值变差;而贝马贝特则显示肝功能测试值提高,并且血清增加的可能性较小肌酐或降低估计的肾小球滤过率。即使与各种他汀类药物同时使用,药物之间的相互作用也极少。此外,与许多传统的贝特类药物(肾排泄型药物)不同,pemafibrate可以排入胆汁,因此即使在肾功能不佳的患者中也可以安全使用,并且血药浓度不会增加。与常规贝特类相比,pema贝特类具有更好的受益风险平衡,可用于难以使用现有贝特类的患者,包括正在服用他汀类药物和肾功能不全的患者。正在进行一项针对2型糖尿病患者的使用Pemafibrate的大规模试验PROMINENT。在当前的审查中,将总结有关匹马贝特的最新数据。

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