Mid-pass Whole-genome Sequencing in a Malagasy Cohort Uncovers Body Composition Associations.

IF 3.3 Q2 GENETICS & HEREDITY HGG Advances Pub Date : 2024-08-20 DOI:10.1016/j.xhgg.2024.100343
Iman Hamid, Séverine Nantenaina Stéphie Raveloson, Germain Jules Spiral, Soanorolalao Ravelonjanahary, Brigitte Marie Raharivololona, José Mahenina Randria, Mosa Zafimaro, Tsiorimanitra Aimée Randriambola, Rota Mamimbahiny Andriantsoa, Tojo Julio Andriamahefa, Bodonomena Fitahiana Laza Rafidison, Mehreen Mughal, Anne-Katrin Emde, Melissa Hendershott, Sarah LeBaron von Baeyer, Kaja A Wasik, Jean Freddy Ranaivoarisoa, Laura Yerges-Armstrong, Stephane E Castel, Rindra Rakotoarivony
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Abstract

The majority of human genomic research studies have been conducted in European-ancestry cohorts, reducing the likelihood of detecting potentially novel and globally impactful findings. Here, we present mid-pass whole-genome sequencing data and a genome-wide association study in a cohort of 264 self-reported Malagasy individuals from three locations on the island of Madagascar. We describe genetic variation in this Malagasy cohort, providing insight into the shared and unique patterns of genetic variation across the island. We observe phenotypic variation by location, and find high rates of hypertension particularly in the Southern Highlands sampling site as well as elevated self-reported malaria prevalence in the West Coast site relative to other sites. After filtering to a subset of 214 minimally-related individuals, we find a number of genetic associations with body composition traits, including many variants that are only observed in African populations or populations with admixed African ancestry from the 1000 Genomes Project. This study highlights the importance of including diverse populations in genomic research for the potential to gain novel insights, even with small cohort sizes. This project was conducted in partnership and consultation with local stakeholders in Madagascar and serves as an example of genomic research that prioritizes community engagement and that has potential impacts on our understanding of human health and disease.

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马达加斯加队列中的中通全基因组测序发现了身体成分关联。
大多数人类基因组研究都是在欧洲巢居队列中进行的,这降低了发现潜在新发现和具有全球影响的发现的可能性。在这里,我们展示了来自马达加斯加岛三个地方的 264 名马达加斯加人的中段全基因组测序数据和一项全基因组关联研究。我们描述了马达加斯加队列中的遗传变异,为了解全岛共同和独特的遗传变异模式提供了见解。我们观察了不同地点的表型变异,发现南部高地采样点的高血压发病率较高,而西海岸采样点的自报疟疾发病率也高于其他采样点。在筛选出 214 个最小相关个体子集后,我们发现了许多与身体成分特征相关的遗传变异,其中包括许多仅在非洲人群或 "千人基因组计划 "中的非洲混血人群中观察到的变异。这项研究强调了将不同人群纳入基因组研究的重要性,因为即使队列规模较小,也有可能获得新的见解。该项目是与马达加斯加当地利益相关者合作和协商开展的,是基因组研究优先考虑社区参与的一个范例,对我们了解人类健康和疾病具有潜在的影响。
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来源期刊
HGG Advances
HGG Advances Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
4.30
自引率
4.50%
发文量
69
审稿时长
14 weeks
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