Genome-wide association studies on malaria in Sub-Saharan Africa: a scoping review

M. Akoth, J. Odhiambo, B. Omolo
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Abstract

Background: Malaria remains one of the leading causes of death in Sub-Saharan Africa (SSA). The scoping review mapped evidence in research on existing studies on malaria genome-wide association studies (GWAS) in SSA. Methods: A scoping review was conducted to investigate the extent of malaria studies in SSA under GWAS. The review followed the methodology for scoping reviews developed by Arksey and OMalley, including identification of research problems, searching for relevant studies, selecting studies, charting data, collating, summarizing, and reporting the findings. Data from relevant studies were collected and synthesized using Excel and Zotero software. The data collected included information on the author, the years of study, the countries of study, the research areas of interest, and the study designs used. Results: Of an initial pool of over 2000 articles retrieved from four databases, namely Google Scholar, PubMed, Scopus, and Web of Science, 569 were retained. After applying the inclusion-exclusion criteria, 99 articles were found to be relevant. Most of these studies (n=25, 60%) used a case-control study design, while the rest used cross-sectional, cohort, longitudinal, family-based, and retrospective designs. These studies were conducted between 2000 and 2023, with a significant increase observed in 2011. Most studies were carried out in Kenya (n = 25), Gambia (n = 17), Cameroon (n = 15), Ghana (n = 12), and Tanzania (n=11), primarily exploring genetic variants associated with malaria susceptibility, resistance, and severity. Conclusion: Many case-control studies in Kenya and Gambia reported genetic variants in malaria susceptibility, resistance, and severity. Few articles were systematic reviews and scoping reviews. GWAS on malaria is scarce in SSA and even fewer studies are model-based. Consequently, there is a pressing need for more genome-wide research on malaria in SSA.
关于撒哈拉以南非洲疟疾的全基因组关联研究:范围审查
背景:疟疾仍然是撒哈拉以南非洲地区(SSA)的主要死因之一。此次范围界定审查对撒哈拉以南非洲现有的疟疾全基因组关联研究(GWAS)的研究证据进行了摸底。方法:进行了一次范围界定审查,以调查撒哈拉以南非洲地区在全基因组关联研究 (GWAS) 项下开展的疟疾研究的范围。综述遵循 Arksey 和 OMalley 制定的范围综述方法,包括确定研究问题、搜索相关研究、选择研究、绘制数据图表、整理、总结和报告研究结果。我们使用 Excel 和 Zotero 软件收集并综合了相关研究的数据。收集的数据包括作者信息、研究年限、研究国家、感兴趣的研究领域以及使用的研究设计。结果:从 Google Scholar、PubMed、Scopus 和 Web of Science 四个数据库中检索到 2000 多篇文章,其中 569 篇被保留下来。在应用了纳入-排除标准后,发现有 99 篇文章是相关的。其中大部分研究(25 篇,占 60%)采用病例对照研究设计,其余研究采用横断面研究、队列研究、纵向研究、基于家庭的研究和回顾性研究设计。这些研究是在 2000 年至 2023 年间进行的,2011 年的研究显著增加。大多数研究在肯尼亚(25 例)、冈比亚(17 例)、喀麦隆(15 例)、加纳(12 例)和坦桑尼亚(11 例)进行,主要探讨与疟疾易感性、抗药性和严重性相关的基因变异。结论肯尼亚和冈比亚的许多病例对照研究报告了疟疾易感性、抗药性和严重程度的遗传变异。很少有文章是系统综述和范围综述。在撒哈拉以南非洲地区,有关疟疾的全球基因组研究很少,基于模型的研究更少。因此,急需对撒哈拉以南非洲地区的疟疾进行更多的全基因组研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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