Falutz Julian, Allas Soraya, Kotler Donald, Thompson Melanie, Koutkia Polyxeni, Albu Jeanine, Trottier Benoit, Routy Jean-Pierre, Cote Pierre, Abribat Thierry, Grinspoon Steven
Montreal General Hospital Immuno-Deficiency Treatment Centre, McGill University Health Center, Montréal, Quebec, Canada.
AIDS. 2005 Aug 12;19(12):1279-87. doi: 10.1097/01.aids.0000180099.35146.30.
To investigate the effects of TH9507, a novel growth hormone releasing factor, on abdominal fat accumulation, metabolic and safety parameters in HIV-infected patients with central fat accumulation.
Randomized, double-blind, placebo-controlled trial enrolling 61 HIV-infected patients with increased waist circumference and waist-to-hip ratio. Participants were randomized to placebo or 1 or 2 mg TH9507 subcutaneously, once daily for 12 weeks. The primary outcome was change in abdominal fat, assessed by dual energy X-ray absorptiometry and cross-sectional computerized tomography scan. Secondary endpoints included change in insulin-like growth factor-I (IGF-I), metabolic, quality of life, and safety parameters.
TH9507 resulted in dose-related physiological increases in IGF-I (P < 0.01 for 1 mg (+48%) and 2 mg (+65%) versus placebo). Trunk fat decreased in the 2 mg group versus placebo (0.8, -4.6 and -9.2%; placebo, 1 and 2 mg, respectively, P = 0.014 for 2 mg versus placebo), without significant change in limb fat. Visceral fat (VAT) decreased most in the 2 mg group (-5.4, -3.6 and -15.7%; placebo, 1 and 2 mg, respectively) but this change was not significant versus placebo. Subcutaneous fat (SAT) was preserved and did not change between or within groups. Lean body mass and the ratio of VAT to SAT improved significantly in both treatment groups versus placebo. Triglyceride and the cholesterol to high-density lipoprotein ratio decreased significantly in the 2 mg group versus placebo. Treatment was generally well tolerated without changes in glucose.
TH9507 reduced truncal fat, improved the lipid profile and did not increase glucose levels in HIV-infected patients with central fat accumulation. TH9507 may be a beneficial treatment strategy in this population, but longer-term studies with more patients are needed to determine effects on VAT, treatment durability, and safety.
研究新型生长激素释放因子TH9507对伴有中心性脂肪堆积的HIV感染患者腹部脂肪堆积、代谢及安全性参数的影响。
一项随机、双盲、安慰剂对照试验,纳入61例腰围和腰臀比增加的HIV感染患者。参与者被随机分为安慰剂组或皮下注射1mg或2mg TH9507组,每日一次,共12周。主要结局是通过双能X线吸收法和横断面计算机断层扫描评估腹部脂肪的变化。次要终点包括胰岛素样生长因子-I(IGF-I)的变化、代谢、生活质量和安全性参数。
TH9507导致IGF-I出现剂量相关的生理性升高(1mg组升高48%,2mg组升高65%,与安慰剂组相比,P<0.01)。与安慰剂组相比,2mg组的躯干脂肪减少(分别为0.8%、-4.6%和-9.2%;安慰剂组、1mg组和2mg组),肢体脂肪无显著变化。2mg组的内脏脂肪(VAT)减少最多(分别为-5.4%、-3.6%和-15.7%;安慰剂组、1mg组和2mg组),但与安慰剂组相比,这一变化无统计学意义。皮下脂肪(SAT)得以保留,组间和组内均无变化。与安慰剂组相比,两个治疗组的瘦体重以及VAT与SAT的比值均显著改善。与安慰剂组相比,2mg组的甘油三酯以及胆固醇与高密度脂蛋白的比值显著降低。治疗耐受性总体良好,血糖无变化。
TH9507可减少伴有中心性脂肪堆积的HIV感染患者的躯干脂肪,改善血脂谱,且不升高血糖水平。TH9507可能是该人群的一种有益治疗策略,但需要更多患者参与的长期研究来确定其对VAT的影响、治疗持久性和安全性。