Seki Mai, Nakano Toshiaki, Tanaka Shigeru, Matsukuma Yuta, Funakoshi Kouta, Ohkuma Toshiaki, Kitazono Takanari
Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.
Center for Cohort Studies, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.
Clin Exp Nephrol. 2023 Apr;27(4):358-364. doi: 10.1007/s10157-023-02322-4. Epub 2023 Feb 4.
Hypertriglyceridemia is increasingly considered a residual risk of cardiovascular disease in patients with chronic kidney disease (CKD). Pemafibrate-a novel selective peroxisome proliferator-activated receptor alpha modulator and a new treatment for hypertriglyceridemia in CKD patients-is reported to have fewer side effects in CKD patients than other fibrates. Appropriate control of hypertriglyceridemia can be expected to improve renal prognosis. However, data on the renal protective effect of pemafibrate are limited. This study aims to evaluate the effectiveness of pemafibrate on urinary protein excretion in CKD patients.
The Pemafibrate, open-label, Randomized cOntrolled study to evaluate the renal protective eFfect In hyperTriglyceridemia patients with Chronic Kidney Disease (PROFIT-CKD) study is an investigator-initiated, multi-center, open-label, parallel-group, randomized controlled trial. Participants are outpatients with hypertriglyceridemia aged 20 years and over, who have received the care of a nephrologist or a diabetologist for more than 3 months. Inclusion criteria include the following: proteinuria (urine protein/creatinine ratio of ≥ 0.15 g/gCr) within three months before allocation, and hypertriglyceridemia (triglycerides ≥ 150 mg/dL and < 1,000 mg/dL) at allocation. In the treatment group, pemafibrate is added to conventional treatment, while conventional treatment is continued with no additional treatment in the control group. Target patient enrollment is 140 patients. The primary endpoint is the change from baseline in the logarithmic urine protein/creatinine ratio at 12 months after study start.
This study will provide new findings on the renal protective effect of pemafibrate in CKD patients.
This clinical trial was registered at the University Hospital Medical Information Network (UMIN) Center (UMIN-CTR: UMIN000042284).
高甘油三酯血症日益被视为慢性肾脏病(CKD)患者心血管疾病的残余风险。 Pemafibrate(一种新型选择性过氧化物酶体增殖物激活受体α调节剂,也是CKD患者高甘油三酯血症的一种新疗法)据报道在CKD患者中比其他贝特类药物副作用更少。适当控制高甘油三酯血症有望改善肾脏预后。然而,关于pemafibrate肾脏保护作用的数据有限。本研究旨在评估pemafibrate对CKD患者尿蛋白排泄的有效性。
Pemafibrate开放标签、随机对照研究以评估慢性肾脏病高甘油三酯血症患者的肾脏保护作用(PROFIT-CKD)研究是一项由研究者发起的多中心、开放标签、平行组、随机对照试验。参与者为年龄20岁及以上的高甘油三酯血症门诊患者,他们接受肾病科医生或糖尿病科医生的治疗超过3个月。纳入标准包括以下内容:分配前三个月内蛋白尿(尿蛋白/肌酐比值≥0.15 g/gCr),以及分配时高甘油三酯血症(甘油三酯≥150 mg/dL且<1000 mg/dL)。在治疗组中,将pemafibrate添加到常规治疗中,而对照组继续进行常规治疗且不进行额外治疗。目标患者入组人数为140名患者。主要终点是研究开始后12个月时对数尿蛋白/肌酐比值相对于基线的变化。
本研究将提供关于pemafibrate对CKD患者肾脏保护作用的新发现。
本临床试验在大学医院医学信息网络(UMIN)中心注册(UMIN-CTR:UMIN000042284)。