雷替格拉韦联合替诺福韦/恩曲他滨对非裔美国人开始HIV治疗的体型、骨密度和血脂的影响

Q2 Medicine HIV Clinical Trials Pub Date : 2015-10-01 Epub Date: 2015-08-07 DOI:10.1179/1945577115Y.0000000002
Laura Young, David A Wohl, William B Hyslop, Yueh Z Lee, Sonia Napravnik, Aimee Wilkin
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引用次数: 10

摘要

背景:雷替格拉韦(Raltegravir)联合替诺福韦/恩曲他滨(TDF/FTC)是一种推荐的初始抗逆转录病毒治疗方案。在美国,大部分被诊断为艾滋病毒感染并开始抗逆转录病毒治疗的人是非裔美国人(AA);然而,该方案对代谢参数的影响主要是在白人患者中研究的。方法:单臂,开放标签研究,未经治疗的AA hiv感染患者给予RAL联合TDF/FTC 104周。在第56周和第104周评估空腹血脂、胰岛素抵抗、内脏脂肪组织(VAT)、腹部皮下脂肪组织(SAT)、四肢和躯干脂肪以及骨矿物质密度(BMD)的变化。结果:纳入30名参与者(85%为男性)。中位入组特征包括年龄38岁,CD4 323个细胞/mm3, HIV RNA水平29,245拷贝/ml,体重指数28.1 kg/m2。在56周和104周时,观察到VAT、躯干脂肪、肢体脂肪和总脂肪显著增加。到第104周,骨密度下降1.5%。非高密度脂蛋白胆固醇、空腹甘油三酯或胰岛素抵抗没有显著变化。CD4细胞计数中位数增加318个细胞/mm3 (IQR 179, 403;结论:在这一AAs队列中,开始RAL与TDF/FTC与脂肪的显著普遍增加有关。血脂或胰岛素抵抗未见明显变化,骨密度略有下降。治疗耐受性良好且有效。这些结果与在不同种族人群中进行初始抗逆转录病毒治疗的研究结果一致,并为开始接受HIV感染治疗的AA患者的治疗选择提供了信息。
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Effects of raltegravir combined with tenofovir/emtricitabine on body shape, bone density, and lipids in African-Americans initiating HIV therapy.

Background: Raltegravir (RAL) plus tenofovir/emtricitabine (TDF/FTC) is a recommended initial antiretroviral regimen. A substantial proportion of persons diagnosed with HIV infection and starting antiretrovirals in the U.S. are African-American (AA); however, the effects of this regimen on metabolic parameters have largely been studied in white patients.

Methods: Single-arm, open-label study of untreated AA HIV-infected patients administered RAL with TDF/FTC for 104 weeks. Changes in fasting lipids, insulin resistance, visceral adipose tissue (VAT), abdominal subcutaneous adipose tissue (SAT), limb and trunk fat, and bone mineral density (BMD) were assessed at weeks 56 and 104.

Results: Thirty (85% men) participants were included. Median entry characteristics included age of 38 years, CD4 323 cells/mm3, HIV RNA level 29,245 copies/ml, and body mass index 28.1 kg/m2. At 56 and 104 weeks, significant increases in VAT, trunk fat, limb fat, and overall fat were observed. Bone mineral density decreased by 1.5% by week 104.There were no significant changes in non-HDL-cholesterol, fasting triglycerides, or insulin resistance. A median CD4 cell count increase of 318 cells/mm3 (IQR 179, 403; full range 40, 749) (P<0.001) was observed. Assuming missing=failure, 78 and 70% had HIV RNA levels<40 copies/ml at weeks 56 and 104, respectively. There were no treatment-related discontinuations and no new antiretroviral resistance mutations were detected.

Conclusions: In this cohort of AAs, initiation of RAL with TDF/FTC was associated with significant general increases in fat. Significant changes in lipids or insulin resistance were not observed and there was a small decline in BMD. Therapy was well tolerated and effective. These results are consistent with findings of studies of initial antiretroviral therapy in racially diverse cohorts and inform treatment selection for AA patients starting therapy for HIV infection.

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来源期刊
HIV Clinical Trials
HIV Clinical Trials 医学-传染病学
CiteScore
1.76
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: HIV Clinical Trials is devoted exclusively to presenting information on the latest developments in HIV/AIDS clinical research. This journal enables readers to obtain the most up-to-date, innovative research from around the world.
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