Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Nephrology, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
J Cachexia Sarcopenia Muscle. 2024 Feb;15(1):401-411. doi: 10.1002/jcsm.13395. Epub 2024 Jan 4.
Chronic inflammation and insulin resistance are highly prevalent in patients on maintenance haemodialysis (MHD) and are strongly associated with protein energy wasting. We conducted a pilot, randomized, placebo-controlled trial of recombinant human interleukin-1 receptor antagonist (IL-1ra) and pioglitazone to explore the safety, feasibility and efficacy for insulin-mediated protein metabolism in patients undergoing MHD.
Twenty-four patients were randomized to receive IL-1ra, pioglitazone or placebo for 12 weeks. Changes in serum inflammatory markers and insulin-mediated protein synthesis, breakdown and net balance in the whole-body and skeletal muscle compartments were assessed using hyperinsulinaemic-hyperaminoacidemic clamp technique at baseline and Week 12.
Among 24 patients, median (interquartile range) age was 51 (40, 61), 79% were African American and 21% had diabetes mellitus. All patients initiated on intervention completed the study, and no serious adverse events were observed. There was a statistically significant decrease in serum high-sensitivity C-reactive protein in the pioglitazone group compared with placebo, but not in the IL-1ra group. No significant differences in the changes of whole-body or skeletal muscle protein synthesis, breakdown and net balance were found between the groups.
In this pilot study, there were no statistically significant effects of 12 weeks of IL-1ra or pioglitazone on protein metabolism in patients on MHD.
gov registration: NCT02278562.
慢性炎症和胰岛素抵抗在维持性血液透析(MHD)患者中非常普遍,并且与蛋白质能量消耗密切相关。我们进行了一项初步的、随机的、安慰剂对照试验,以研究重组人白细胞介素-1 受体拮抗剂(IL-1ra)和吡格列酮对 MHD 患者胰岛素介导的蛋白质代谢的安全性、可行性和疗效。
24 名患者被随机分为接受 IL-1ra、吡格列酮或安慰剂治疗 12 周。使用高胰岛素-高氨基酸钳夹技术在基线和第 12 周评估血清炎症标志物和胰岛素介导的全身和骨骼肌蛋白质合成、分解和净平衡的变化。
24 名患者中,中位数(四分位距)年龄为 51 岁(40 岁,61 岁),79%为非裔美国人,21%患有糖尿病。所有开始干预的患者均完成了研究,未观察到严重不良事件。与安慰剂组相比,吡格列酮组血清高敏 C 反应蛋白显著下降,但 IL-1ra 组无显著差异。各组间全身或骨骼肌蛋白质合成、分解和净平衡的变化无显著差异。
在这项初步研究中,12 周的 IL-1ra 或吡格列酮治疗对 MHD 患者的蛋白质代谢没有统计学显著影响。
gov 注册:NCT02278562。