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

IF 2.9 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-05-16 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0309268
Morine Akoth, John Odhiambo, Bernard Omolo
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引用次数: 0

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 map existing studies in genome-wide association on malaria in SSA, with a review period between 1st January 2000 and 31st December 2024. The searches were made with the last search done in January 2025. The extracted data were analyzed using R software and SRplot. Relevant studies were identified through electronic searching of Google Scholar, Pubmed, Scopus, and Web of Science databases. Two independent reviewers followed the inclusion-exclusion criteria to extract relevant studies. Data from the studies were collected and synthesized using Excel and Zotero software.

Results: We identified 89 studies for inclusion. Most of these studies (n = 42, [Formula: see text]) used a case-control study design, while the rest used cross-sectional, cohort, longitudinal, family-based, and experimental study designs. These studies were conducted between 2000 and 2024, with a noticeable increase in publications from 2012. Most studies were carried out in Kenya (n = 23), Gambia (n = 18), Cameroon (n = 15), and Tanzania (n = 9), 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. 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.

撒哈拉以南非洲疟疾全基因组关联研究:范围综述。
背景:疟疾仍然是撒哈拉以南非洲(SSA)的主要死亡原因之一。本综述对SSA疟疾全基因组关联研究(GWAS)现有研究的证据进行了梳理。方法:以2000年1月1日至2024年12月31日为回顾期,对SSA地区疟疾全基因组关联的现有研究进行综述。最后一次搜索是在2025年1月进行的。提取的数据采用R软件和SRplot进行分析。通过b谷歌Scholar、Pubmed、Scopus和Web of Science数据库的电子检索,确定相关研究。两名独立审稿人按照纳入-排除标准提取相关研究。使用Excel和Zotero软件对研究数据进行收集和综合。结果:我们确定了89项研究纳入。大多数研究(n = 42,[公式:见文本])采用病例对照研究设计,其余研究采用横断面、队列、纵向、基于家庭和实验研究设计。这些研究是在2000年至2024年间进行的,从2012年开始,出版物明显增加。大多数研究在肯尼亚(n = 23)、冈比亚(n = 18)、喀麦隆(n = 15)和坦桑尼亚(n = 9)开展,主要探索与疟疾易感性、耐药性和严重程度相关的遗传变异。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、耐药性和严重程度的遗传变异。关于疟疾的GWAS在SSA很少,基于模型的研究更少。因此,迫切需要开展SSA地区疟疾全基因组研究。
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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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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