Suppr超能文献

利用大量异构数据评估撒哈拉以南非洲关键人群中艾滋病应对措施的潜在影响:博洛卡数据存储库倡议方案

Harnessing Big Heterogeneous Data to Evaluate the Potential Impact of HIV Responses Among Key Populations in Sub-Saharan Africa: Protocol for the Boloka Data Repository Initiative.

作者信息

Phaswana Mafuya Refilwe Nancy, Phalane Edith, Rao Amrita, Willis Kalai, Rucinski Katherine, Voet K Alida, Abdulrahman Amal, Siyamayambo Claris, Sebati Betty, Seloka Mohlago, Jaiteh Musa, Olifant Lerato Lucia, Journeay Katharine, Sisel Haley, Li Xiaoming, Olatosi Bankole, Hikmet Neset, Duhoon Prashant, Wolmarans Francois, Shiferaw Yegnanew A, Motsieloa Lifutso, Rampilo Mashudu, Baral Stefan

机构信息

South African Medical Research Council/University of Johannesburg Pan African Centre for Epidemics Research Extramural Unit, University of Johannesburg, Johannesburg, South Africa.

Department of Health Services Policy Management, Arnold School of Public Health, University of South Carolina, Columbia, SC, United States.

出版信息

JMIR Res Protoc. 2025 Jan 22;14:e63583. doi: 10.2196/63583.

Abstract

BACKGROUND

In South Africa, there is no centralized HIV surveillance system where key populations (KPs) data, including gay men and other men who have sex with men, female sex workers, transgender persons, people who use drugs, and incarcerated persons, are stored in South Africa despite being on higher risk of HIV acquisition and transmission than the general population. Data on KPs are being collected on a smaller scale by numerous stakeholders and managed in silos. There exists an opportunity to harness a variety of data, such as empirical, contextual, observational, and programmatic data, for evaluating the potential impact of HIV responses among KPs in South Africa.

OBJECTIVE

This study aimed to leverage and harness big heterogeneous data on HIV among KPs and harmonize and analyze it to inform a targeted HIV response for greater impact in Sub-Saharan Africa.

METHODS

The Boloka data repository initiative has 5 stages. There will be engagement of a wide range of stakeholders to facilitate the acquisition of data (stage 1). Through these engagements, different data types will be collated (stage 2). The data will be filtered and screened to enable high-quality analyses (stage 3). The collated data will be stored in the Boloka data repository (stage 4). The Boloka data repository will be made accessible to stakeholders and authorized users (stage 5).

RESULTS

The protocol was funded by the South African Medical Research Council following external peer reviews (December 2022). The study received initial ethics approval (May 2022), renewal (June 2023), and amendment (July 2024) from the University of Johannesburg (UJ) Research Ethics Committee. The research team has been recruited, onboarded, and received non-web-based internet ethics training (January 2023). A list of current and potential data partners has been compiled (January 2023 to date). Data sharing or user agreements have been signed with several data partners (August 2023 to date). Survey and routine data have been and are being secured (January 5, 2023). In (September 2024) we received Ghana Men Study data. The data transfer agreement between the Pan African Centre for Epidemics Research and the Perinatal HIV Research Unit was finalized (October 2024), and we are anticipating receiving data by (December 2024). In total, 7 abstracts are underway, with 1 abstract completed the analysis and expected to submit the full article to the peer-reviewed journal in early January 2024. As of March 2025, we expect to submit the remaining 6 full articles.

CONCLUSIONS

A truly "complete" data infrastructure that systematically and rigorously integrates diverse data for KPs will not only improve our understanding of local epidemics but will also improve HIV interventions and policies. Furthermore, it will inform future research directions and become an incredible institutional mechanism for epidemiological and public health training in South Africa and Sub-Saharan Africa.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/63583.

摘要

背景

在南非,尽管男同性恋者及其他与男性发生性行为的男性、女性性工作者、跨性别者、吸毒者和被监禁者等重点人群感染和传播艾滋病毒的风险高于普通人群,但南非却没有一个集中的艾滋病毒监测系统来存储这些人群的数据。众多利益相关者正在小规模收集重点人群的数据,并各自为政地进行管理。利用各种数据(如实证数据、背景数据、观察数据和项目数据)来评估南非针对重点人群的艾滋病毒应对措施的潜在影响,这一机会是存在的。

目的

本研究旨在利用重点人群中有关艾滋病毒的大量异构数据,对其进行整合与分析,为撒哈拉以南非洲地区更具影响力的针对性艾滋病毒应对措施提供依据。

方法

博洛卡数据存储库计划有5个阶段。将与广泛的利益相关者进行接触,以促进数据获取(第1阶段)。通过这些接触,将整理不同类型的数据(第2阶段)。对数据进行过滤和筛选,以实现高质量分析(第3阶段)。整理后的数据将存储在博洛卡数据存储库中(第4阶段)。博洛卡数据存储库将对利益相关者和授权用户开放(第5阶段)。

结果

该方案在外部同行评审后(2022年12月)由南非医学研究理事会资助。该研究获得了约翰内斯堡大学(UJ)研究伦理委员会的初始伦理批准(2022年5月)、延期批准(2023年6月)和修订批准(2024年7月)。研究团队已组建、入职并接受了非网络形式的互联网伦理培训(2023年1月)。已编制了当前和潜在数据合作伙伴的名单(2023年1月至今)。已与多个数据合作伙伴签署了数据共享或用户协议(2023年8月至今)。调查数据和常规数据已得到并正在得到妥善保管(2023年1月5日)。2024年9月,我们收到了加纳男性研究数据。泛非流行病研究中心与围产期艾滋病毒研究单位之间的数据转移协议已敲定(2024年10月),预计2024年12月前会收到数据。目前共有7篇摘要正在撰写,其中1篇摘要已完成分析,预计2024年1月初将全文提交给同行评审期刊。截至2025年3月,我们预计提交其余6篇全文。

结论

一个真正“完整”的数据基础设施,若能系统且严格地整合重点人群的各类数据,不仅会增进我们对当地疫情的了解,还将改善艾滋病毒干预措施和政策。此外,它将为未来的研究方向提供信息,并成为南非和撒哈拉以南非洲地区进行流行病学和公共卫生培训的绝佳机构机制。

国际注册报告识别码(IRRID):DERR1-10.2196/63583

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/396e/11799808/37b7a7f178c9/resprot_v14i1e63583_fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验