Infectious Diseases Institute, Makerere University, Kampala, Uganda.
Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.
PLoS One. 2022 Mar 2;17(3):e0264792. doi: 10.1371/journal.pone.0264792. eCollection 2022.
Poeple living with HIV have higher prevalence of diabetes mellitus and metabolic perturbations compared to non-HIV populations. Diabetes and metabolic syndrome co-morbidities add significant burden to HIV care. Currently, WHO recommends integrase strand transfer inhibitors (INSTIs) as the first or second line therapy in people with HIV due to overall good tolerability and safety profile. However, whether INSTI use increases the risk of incident diabetes (with or without metabolic syndrome) compared to other anti-retroviral therapies (ART) is controversial. In this systematic review and meta-analysis, we aim to examine this risk in HIV-positive populations receiving INSTIs compared to other ART regimens (not containing INSTIs).
The study will be reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) statement and the Meta-analysis Of Observational Studies in Epidemiology (MOOSE) guidelines. This protocol adheres to the Standard Protocol Items for reporting systematic reviews and meta-analyses checklist. Eligibility criteria will be original peer-reviewed published articles and conference abstracts with no language or geographical restriction; that report the ocurrence of diabetes mellitus as a discrete outcome or part of metabolic syndrome, in adult PLWHIV receiving INSTIs compared to other ART regimens. PubMed/ Medline, Web of Science, Embase and Cochrane Database of Systematic Reviews will be searched from 1st- January-2000 to 31st-January-2022. Per our a priori, screening, inclusion and data extraction will be conducted separately by two investigators, and a senior researcher will be consulted in case of disagreement. The quality of included studies will be assessed by the Newcastle-Ottawa Scale (NOS) for cohort and case-control studies and the revised Cochrane risk-of-bias tool (ROB2) for randomized controlled trials. The quantitative synthesis of the study outcomes will be explored in different subgroups and sensitivity analyses. Meta regression will also be performed to further test the predictors of the outcome.
Ethical approval is waived as the study is a review of published litterature. The analyses will be presented in conferences and published as a scientific article.
PROSPERO registration number is; CRD42021273040.
与非 HIV 人群相比,HIV 感染者中糖尿病和代谢紊乱的患病率更高。糖尿病和代谢综合征合并症给 HIV 护理带来了巨大负担。目前,世界卫生组织(WHO)建议将整合酶抑制剂(INSTIs)作为 HIV 感染者的一线或二线治疗药物,因为其总体耐受性和安全性良好。然而,与其他抗逆转录病毒疗法(ART)相比,INSTI 的使用是否会增加新发糖尿病(无论是否合并代谢综合征)的风险仍存在争议。在这项系统评价和荟萃分析中,我们旨在检查接受 INSTIs 的 HIV 阳性人群与接受其他不含 INSTIs 的 ART 方案相比,发生这种风险的情况。
该研究将按照系统评价和荟萃分析的首选报告项目(PRISMA)声明和观察性研究荟萃分析(MOOSE)指南进行报告。本方案遵循系统评价和荟萃分析标准报告项目清单。纳入标准为原始同行评议发表的文章和会议摘要,无语言或地理限制;报告糖尿病作为离散结局或代谢综合征的一部分,在接受 INSTIs 的成年 HIV 感染者中与其他 ART 方案相比。将从 2000 年 1 月 1 日至 2022 年 1 月 31 日在 PubMed/Medline、Web of Science、Embase 和 Cochrane 系统评价数据库中进行检索。根据我们的事先计划,两名研究人员将分别进行筛选、纳入和数据提取,如果意见不一致,将咨询一位资深研究人员。将使用纽卡斯尔-渥太华量表(NOS)对队列和病例对照研究以及修订后的 Cochrane 偏倚风险工具(ROB2)对随机对照试验进行纳入研究质量评估。将在不同亚组和敏感性分析中探索研究结果的定量综合。还将进行荟萃回归以进一步测试结局的预测因子。
由于本研究是对已发表文献的综述,因此豁免伦理批准。分析结果将在会议上进行汇报,并作为科学文章发表。
PROSPERO 注册号为:CRD42021273040。