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资源有限环境下抗逆转录病毒治疗推出后治疗初治 HIV 感染者的抗逆转录病毒耐药全球趋势:一项全球协作研究和荟萃回归分析。

Global trends in antiretroviral resistance in treatment-naive individuals with HIV after rollout of antiretroviral treatment in resource-limited settings: a global collaborative study and meta-regression analysis.

机构信息

Department of Infection, University College London, London, UK.

出版信息

Lancet. 2012 Oct 6;380(9849):1250-8. doi: 10.1016/S0140-6736(12)61038-1. Epub 2012 Jul 23.


DOI:10.1016/S0140-6736(12)61038-1
PMID:22828485
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3790969/
Abstract

BACKGROUND: The emergence and spread of high levels of HIV-1 drug resistance in resource-limited settings where combination antiretroviral treatment has been scaled up could compromise the effectiveness of national HIV treatment programmes. We aimed to estimate changes in the prevalence of HIV-1 drug resistance in treatment-naive individuals with HIV since initiation of rollout in resource-limited settings. METHODS: We did a systematic search for studies and conference abstracts published between January, 2001, and July, 2011, and included additional data from the WHO HIV drug resistance surveillance programme. We assessed the prevalence of drug-resistance mutations in untreated individuals with respect to time since rollout in a series of random-effects meta-regression models. FINDINGS: Study-level data were available for 26,102 patients from sub-Saharan Africa, Asia, and Latin America. We recorded no difference between chronic and recent infection on the prevalence of one or more drug-resistance mutations for any region. East Africa had the highest estimated rate of increase at 29% per year (95% CI 15 to 45; p=0·0001) since rollout, with an estimated prevalence of HIV-1 drug resistance at 8 years after rollout of 7·4% (4·3 to 12·7). We recorded an annual increase of 14% (0% to 29%; p=0·054) in southern Africa and a non-significant increase of 3% (-0·9 to 16; p=0·618) in west and central Africa. There was no change in resistance over time in Latin America, and because of much country-level heterogeneity the meta-regression analysis was not appropriate for Asia. With respect to class of antiretroviral, there were substantial increases in resistance to non-nucleoside reverse transcriptase inhibitors (NNRTI) in east Africa (36% per year [21 to 52]; p<0·0001) and southern Africa (23% per year [7 to 42]; p=0·0049). No increase was noted for the other drug classes in any region. INTERPRETATION: Our findings suggest a significant increase in prevalence of drug resistance over time since antiretroviral rollout in regions of sub-Saharan Africa; this rise is driven by NNRTI resistance in studies from east and southern Africa. The findings are of concern and draw attention to the need for enhanced surveillance and drug-resistance prevention efforts by national HIV treatment programmes. Nevertheless, estimated levels, although increasing, are not unexpected in view of the large expansion of antiretroviral treatment coverage seen in low-income and middle-income countries--no changes in antiretroviral treatment guidelines are warranted at the moment. FUNDING: Bill & Melinda Gates Foundation and the European Community's Seventh Framework Programme.

摘要

背景:在资源有限的环境中,艾滋病毒-1 高耐药水平的出现和传播,可能会削弱国家艾滋病毒治疗规划的有效性,而这些地方已经扩大了联合抗逆转录病毒治疗。我们旨在评估自资源有限环境中推出以来,新感染艾滋病毒的未经治疗个体中艾滋病毒-1 耐药性的流行率变化。

方法:我们进行了一项系统搜索,以检索 2001 年 1 月至 2011 年 7 月间发表的研究和会议摘要,并纳入了世卫组织艾滋病毒耐药性监测计划的额外数据。我们在一系列随机效应荟萃回归模型中,根据推出后的时间评估了未经治疗的个体中耐药突变的流行率。

结果:我们从撒哈拉以南非洲、亚洲和拉丁美洲获得了 26102 名患者的研究水平数据。我们发现,对于任何地区,慢性感染和近期感染之间在一个或多个耐药突变的流行率上没有差异。东非的估计增长率最高,为每年 29%(95%CI 15 至 45;p=0·0001),推出后 8 年的艾滋病毒-1 耐药率估计为 7.4%(4.3 至 12.7)。我们记录到南部非洲每年增加 14%(0%至 29%;p=0·054),而西部和中部非洲则没有显著增加 3%(-0·9 至 16;p=0·618)。拉丁美洲的耐药率没有随时间变化,由于各国之间存在很大的异质性,因此元回归分析不适用于亚洲。就抗逆转录病毒药物类别而言,东非(每年 36%[21 至 52];p<0·0001)和南部非洲(每年 23%[7 至 42];p=0·0049)的非核苷类逆转录酶抑制剂(NNRTI)耐药性显著增加。在任何地区,其他药物类别的耐药性均未增加。

解释:我们的研究结果表明,自抗逆转录病毒推出以来,撒哈拉以南非洲地区耐药率随时间显著上升;这种上升是由东非和南非的研究中的 NNRTI 耐药性驱动的。这一发现令人担忧,提醒人们需要加强国家艾滋病毒治疗规划的监测和耐药性预防工作。尽管如此,考虑到低收入和中等收入国家抗逆转录病毒治疗覆盖率的大幅扩大,预计水平虽然有所上升,但并非出乎意料——目前不需要改变抗逆转录病毒治疗指南。

资金来源:比尔及梅琳达·盖茨基金会和欧盟第七框架计划。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/19130e1f6cf9/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/86d7500395ff/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/b326137c6ce6/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/1acd15308d4d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/19130e1f6cf9/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/86d7500395ff/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/b326137c6ce6/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/1acd15308d4d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ab5/3790969/19130e1f6cf9/gr4.jpg

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