Cavalcanti Rodrigo B, Raboud Janet, Shen Sandy, Kain Kevin C, Cheung Angela, Walmsley Sharon
Department of Medicine and McLaughlin-Rotman Centre, University Health Network, Toronto, ON, M5T 2S8, Canada.
J Infect Dis. 2007 Jun 15;195(12):1754-61. doi: 10.1086/518005. Epub 2007 May 2.
Thiazolidinediones such as rosiglitazone may have benefit in ameliorating human immunodeficiency virus (HIV) lipoatrophy.
HIV-positive patients receiving stable, protease inhibitor-containing highly active antiretroviral therapy with HIV lipodystrophy were prospectively randomized to rosiglitazone (4 mg/day) or placebo. The primary end point was the 24-week percentage change in arm fat by dual-energy x-ray absorptiometry (DEXA). Clinical and anthropometric evaluations, fasting lipid parameters, oral glucose tolerance testing, CD36 expression, quality of life measures, and DEXA scanning were performed at baseline and week 24.
Seventy-eight of the 96 enrolled patients were evaluated. Median age was 46.8 years, 97.4% were male, and 54% were treated with thymidine analogues. Median baseline limb fat was 3.76 and 2.99 kg in the rosiglitazone and control groups, respectively. Median changes in arm, leg, trunk, and total body fat at 24 weeks were not significantly different between groups (7.1% vs. 5.0% [P=.94]; 0.1% vs. -2.4% [P=.90]; 1.2% vs. -1.4% [P=.81]; and 1.7% vs. 0.4% [P=.76]). There were no significant changes in secondary end points. There was no correlation between changes in body fat or treatment-arm and CD36 expression.
This randomized, placebo-controlled trial did not show benefit of 4 mg/day of rosiglitazone on lipoatrophy or metabolic parameters in patients with HIV lipodystrophy.
噻唑烷二酮类药物如罗格列酮可能有助于改善人类免疫缺陷病毒(HIV)相关脂肪萎缩。
将接受含蛋白酶抑制剂的稳定高效抗逆转录病毒治疗且伴有HIV脂肪代谢障碍的HIV阳性患者前瞻性随机分为罗格列酮组(4毫克/天)和安慰剂组。主要终点是通过双能X线吸收法(DEXA)测量的24周时手臂脂肪百分比变化。在基线和第24周进行临床和人体测量评估、空腹血脂参数、口服葡萄糖耐量试验、CD36表达、生活质量测量以及DEXA扫描。
96名入组患者中的78名接受了评估。中位年龄为46.8岁,97.4%为男性,54%接受胸腺嘧啶类似物治疗。罗格列酮组和对照组的中位基线肢体脂肪分别为3.76千克和2.99千克。24周时两组在手臂、腿部、躯干和全身脂肪的中位变化无显著差异(7.1%对5.0%[P = 0.94];0.1%对 -2.4%[P = 0.90];1.2%对 -1.4%[P = 0.81];1.7%对0.4%[P = 0.76])。次要终点无显著变化。体脂变化或治疗组与CD36表达之间无相关性。
这项随机、安慰剂对照试验未显示每天4毫克罗格列酮对HIV脂肪代谢障碍患者的脂肪萎缩或代谢参数有益处。