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乌干达开始抗逆转录病毒疗法的成年人中的 HIV 耐药性。

HIV drug resistance among adults initiating antiretroviral therapy in Uganda.

机构信息

Uganda Virus Research Institute (UVRI), Entebbe, Uganda.

Medical Research Council (MRC)/UVRI and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.

出版信息

J Antimicrob Chemother. 2021 Aug 12;76(9):2407-2414. doi: 10.1093/jac/dkab159.

Abstract

BACKGROUND

WHO revised their HIV drug resistance (HIVDR) monitoring strategy in 2014, enabling countries to generate nationally representative HIVDR prevalence estimates from surveys conducted using this methodology. In 2016, we adopted this strategy in Uganda and conducted an HIVDR survey among adults initiating or reinitiating ART.

METHODS

A cross-sectional survey of adults aged ≥18 years initiating or reinitiating ART was conducted at 23 sites using a two-stage cluster design sampling method. Participants provided written informed consent prior to enrolment. Whole blood collected in EDTA vacutainer tubes was used for preparation of dried blood spot (DBS) specimens or plasma. Samples were shipped from the sites to the Central Public Health Laboratory (CPHL) for temporary storage before transfer to the Uganda Virus Research Institute (UVRI) for genotyping. Prevalence of HIVDR among adults initiating or reinitiating ART was determined.

RESULTS

Specimens from 491 participants (median age 32 years and 61.5% female) were collected between August and December 2016. Specimens from 351 participants were successfully genotyped. Forty-nine had drug resistance mutations, yielding an overall weighted HIVDR prevalence of 18.2% with the highest noted for NNRTIs at 14.1%.

CONCLUSIONS

We observed a high HIVDR prevalence for NNRTIs among adults prior to initiating or reinitiating ART in Uganda. This is above WHO's recommended threshold of 10% when countries should consider changing from NNRTI- to dolutegravir-based first-line regimens. This recommendation was adopted in the revised Ugandan ART guidelines. Dolutegravir-containing ART regimens are preferred for first- and second-line ART regimens.

摘要

背景

世界卫生组织(WHO)于 2014 年修订了其艾滋病毒耐药性(HIVDR)监测策略,使各国能够使用该方法进行的调查来生成具有全国代表性的 HIVDR 流行率估计。2016 年,我们在乌干达采用了这一策略,并对开始或重新开始接受抗逆转录病毒治疗(ART)的成年人进行了 HIVDR 调查。

方法

采用两阶段整群抽样方法,在 23 个地点对年龄≥18 岁开始或重新开始接受 ART 的成年人进行横断面调查。参与者在入组前提供书面知情同意书。使用 EDTA 真空采血管采集的全血用于制备干血斑(DBS)标本或血浆。样本从现场运送到中央公共卫生实验室(CPHL)进行临时储存,然后转移到乌干达病毒研究所(UVRI)进行基因分型。确定开始或重新开始接受 ART 的成年人中 HIVDR 的流行率。

结果

2016 年 8 月至 12 月期间共采集了 491 名参与者(中位年龄 32 岁,61.5%为女性)的标本。351 名参与者的标本成功进行了基因分型。49 名参与者发生了耐药突变,总体加权 HIVDR 流行率为 18.2%,其中 NNRTIs 最高,为 14.1%。

结论

我们观察到乌干达开始或重新开始接受 ART 的成年人中 NNRTIs 的 HIVDR 流行率很高。这高于 WHO 建议的 10%阈值,当国家应考虑将 NNRTI 改为多替拉韦为基础的一线治疗方案时。这一建议已被修订后的乌干达抗逆转录病毒治疗指南采纳。多替拉韦包含的 ART 方案是首选的一线和二线 ART 方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cefc/8361362/2a663ee11172/dkab159f1.jpg

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