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AIDS Res Hum Retroviruses. 2020 Oct;36(10):831-834. doi: 10.1089/AID.2019.0290. Epub 2020 Aug 27.
2
Greater decrease in bone mineral density with protease inhibitor regimens compared with nonnucleoside reverse transcriptase inhibitor regimens in HIV-1 infected naive patients.在初治的HIV-1感染患者中,与非核苷类逆转录酶抑制剂方案相比,蛋白酶抑制剂方案导致的骨矿物质密度下降幅度更大。
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本文引用的文献

1
Antiretroviral Therapy Containing HIV Protease Inhibitors Enhances Fracture Risk by Impairing Osteoblast Differentiation and Bone Quality.含有HIV蛋白酶抑制剂的抗逆转录病毒疗法通过损害成骨细胞分化和骨质量增加骨折风险。
J Infect Dis. 2017 Jun 15;215(12):1893-1897. doi: 10.1093/infdis/jix246.
2
The protease inhibitors and HIV-associated bone loss.蛋白酶抑制剂与HIV相关的骨质流失。
Curr Opin HIV AIDS. 2016 May;11(3):333-42. doi: 10.1097/COH.0000000000000260.
3
Body Composition Changes After Initiation of Raltegravir or Protease Inhibitors: ACTG A5260s.拉替拉韦或蛋白酶抑制剂起始治疗后的身体成分变化:ACTG A5260s研究
Clin Infect Dis. 2016 Apr 1;62(7):853-62. doi: 10.1093/cid/ciw017. Epub 2016 Jan 20.
4
Changes in Bone Mineral Density After Initiation of Antiretroviral Treatment With Tenofovir Disoproxil Fumarate/Emtricitabine Plus Atazanavir/Ritonavir, Darunavir/Ritonavir, or Raltegravir.使用富马酸替诺福韦二吡呋酯/恩曲他滨联合阿扎那韦/利托那韦、达芦那韦/利托那韦或拉替拉韦起始抗逆转录病毒治疗后骨矿物质密度的变化。
J Infect Dis. 2015 Oct 15;212(8):1241-9. doi: 10.1093/infdis/jiv194. Epub 2015 May 5.
5
Recommendations for evaluation and management of bone disease in HIV.关于HIV患者骨病评估与管理的建议。
Clin Infect Dis. 2015 Apr 15;60(8):1242-51. doi: 10.1093/cid/civ010. Epub 2015 Jan 21.
6
Osteoporosis and fractures in HIV/hepatitis C virus coinfection: a systematic review and meta-analysis.HIV/丙型肝炎病毒合并感染中的骨质疏松症和骨折:一项系统评价和荟萃分析。
AIDS. 2014 Sep 10;28(14):2119-31. doi: 10.1097/QAD.0000000000000363.
7
Body composition changes after switching from protease inhibitors to raltegravir: SPIRAL-LIP substudy.从蛋白酶抑制剂转换为拉替拉韦后身体成分的变化:SPIRAL-LIP 子研究。
AIDS. 2012 Feb 20;26(4):475-81. doi: 10.1097/QAD.0b013e32834f3507.
8
Simulated increases in body fat and errors in bone mineral density measurements by DXA and QCT.DXA 和 QCT 测量体脂肪增加和骨密度测量误差的模拟。
J Bone Miner Res. 2012 Jan;27(1):119-24. doi: 10.1002/jbmr.506.
9
Peripheral and central fat changes in subjects randomized to abacavir-lamivudine or tenofovir-emtricitabine with atazanavir-ritonavir or efavirenz: ACTG Study A5224s.接受阿巴卡韦-拉米夫定或替诺福韦-恩曲他滨联合阿扎那韦/利托那韦或依非韦伦治疗的受试者外周和中心脂肪变化:ACTG 研究 A5224s。
Clin Infect Dis. 2011 Jul 15;53(2):185-96. doi: 10.1093/cid/cir324.
10
Bone mineral density and fractures in antiretroviral-naive persons randomized to receive abacavir-lamivudine or tenofovir disoproxil fumarate-emtricitabine along with efavirenz or atazanavir-ritonavir: Aids Clinical Trials Group A5224s, a substudy of ACTG A5202.在接受依非韦伦或阿扎那韦-利托那韦联合治疗的抗逆转录病毒初治患者中,随机分配接受阿巴卡韦-拉米夫定或替诺福韦酯-富马酸二吡呋酯-恩曲他滨:艾滋病临床治疗试验组 A5224s,A5202 的子研究。
J Infect Dis. 2011 Jun 15;203(12):1791-801. doi: 10.1093/infdis/jir188.

短篇通讯:脂肪变化对起始抗逆转录病毒治疗时蛋白酶抑制剂对腰椎骨密度变化影响的作用。

Short Communication: Impact of Fat Changes on the Effect of Protease Inhibitors on Lumbar Spine Bone Mineral Density Changes with Antiretroviral Therapy Initiation.

机构信息

Division of Endocrinology, Diabetes, & Metabolism, Johns Hopkins University, Baltimore, Maryland, USA.

Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

出版信息

AIDS Res Hum Retroviruses. 2020 Oct;36(10):831-834. doi: 10.1089/AID.2019.0290. Epub 2020 Aug 27.

DOI:10.1089/AID.2019.0290
PMID:32623904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7548021/
Abstract

People living with HIV (PLWH) who are on protease inhibitor (PI)-containing regimens have been shown to have increases in visceral adipose tissue (VAT) and a greater decrease in spine bone mineral density (BMD) than those receiving non-PI regimens when initiating treatment. This increase in VAT has been hypothesized to falsely lower spine BMD measured via dual-energy X-ray absorptiometry, suggesting that the PI-associated BMD loss is an artefact rather than real. To test this, data collected from two completed 96-week clinical trials, AIDS Clinical Trial Group studies A5224s and A5260s, of antiretroviral therapy-naive PLWH initiating treatment with PI and non-PI-containing regimens were analyzed comparing VAT accumulation and spine BMD loss. Results showed no significant decrease in spine BMD in persons in the highest quartile (Q4) of VAT gain versus the rest of the study population (Q1-3) in either the PI and non-PI arms, suggesting that PI-associated BMD loss is not likely to be an artefact of overlying VAT.

摘要

接受含蛋白酶抑制剂 (PI) 治疗方案的艾滋病毒感染者 (PLWH) 与接受非 PI 治疗方案的患者相比,在开始治疗时,内脏脂肪组织 (VAT) 增加,脊柱骨密度 (BMD) 下降更多。这种 VAT 的增加被假设为通过双能 X 射线吸收法测量的脊柱 BMD 降低,这表明 PI 相关的 BMD 丢失是一种假象,而不是真实的。为了验证这一点,分析了来自两项已完成的 96 周临床试验(艾滋病临床试验组研究 A5224s 和 A5260s)的数据,这些研究是针对开始接受 PI 和非 PI 治疗方案的抗逆转录病毒治疗初治的 PLWH。结果显示,在 PI 和非 PI 组中,与研究人群的其余部分(Q1-3)相比,VAT 增加最高四分位 (Q4) 的人群的脊柱 BMD 无明显下降,这表明 PI 相关的 BMD 丢失不太可能是 VAT 覆盖的假象。