Bando Hidenori, Taneda Shinji, Manda Naoki
Manda Memorial Hospital, Sapporo City, Hokkaido, Japan.
JMA J. 2021 Apr 15;4(2):135-140. doi: 10.31662/jmaj.2020-0104. Epub 2021 Mar 26.
Pemafibrate is a potent selective peroxisome proliferator-activated receptor α (PPARα) modulator that may be safer than conventional PPARα agonists in the treatment of dyslipidemia. This study was designed to investigate the efficacy of low-dose pemafibrate (0.1 mg/day) therapy for hypertriglyceridemia in 31 patients with type 2 diabetes and high triglyceride (TG) levels at the Manda Memorial Hospital.
TG, remnant lipoprotein cholesterol (RLP-C), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), apolipoprotein (Apo) AI, Apo AII, Apo B, Apo CII, Apo CIII, and Apo E levels were evaluated. Liver, kidney, and muscle toxicity tests were also performed. Pemafibrate (0.1 mg) was administered once daily.
This treatment significantly decreased TG, RLP-C, Apo CII, Apo CIII, and Apo E levels while significantly increasing HDL-C, Apo AI, and Apo AII levels. No significant changes were observed in LDL-C and Apo B levels. There were no significant liver-, kidney-, or muscle-related adverse events.
The results of this study show that low-dose pemafibrate administration improves the lipid profile in Japanese patients with hypertriglyceridemia and type 2 diabetes.
佩马贝特是一种强效的选择性过氧化物酶体增殖物激活受体α(PPARα)调节剂,在治疗血脂异常方面可能比传统的PPARα激动剂更安全。本研究旨在调查在曼达纪念医院对31例2型糖尿病且甘油三酯(TG)水平高的患者采用低剂量佩马贝特(0.1毫克/天)治疗高甘油三酯血症的疗效。
评估了TG、残留脂蛋白胆固醇(RLP-C)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、载脂蛋白(Apo)AI、Apo AII、Apo B、Apo CII、Apo CIII和Apo E水平。还进行了肝、肾和肌肉毒性测试。佩马贝特(0.1毫克)每日给药一次。
该治疗显著降低了TG、RLP-C、Apo CII、Apo CIII和Apo E水平,同时显著提高了HDL-C、Apo AI和Apo AII水平。LDL-C和Apo B水平未观察到显著变化。未出现与肝、肾或肌肉相关的显著不良事件。
本研究结果表明,低剂量佩马贝特给药可改善日本高甘油三酯血症和2型糖尿病患者的血脂谱。