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在马达加斯加队列中进行中程全基因组测序揭示了身体成分的关联。

Mid-pass whole-genome sequencing in a Malagasy cohort uncovers body composition associations.

机构信息

Variant Bio, Inc., Seattle, WA 98109, USA.

University of Antananarivo, Faculty of Sciences, Mention Anthropobiologie et Développement Durable, Antananarivo 101, Madagascar.

出版信息

HGG Adv. 2024 Oct 10;5(4):100343. doi: 10.1016/j.xhgg.2024.100343. Epub 2024 Aug 22.

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 potentially impacts our understanding of human health and disease.

摘要

大多数人类基因组研究都是在欧洲血统的队列中进行的,这降低了发现潜在新颖且具有全球影响力的发现的可能性。在这里,我们展示了来自马达加斯加岛三个地点的 264 名自我报告的马达加斯加个体的中程全基因组测序数据和全基因组关联研究。我们描述了该马达加斯加队列中的遗传变异,深入了解了整个岛屿上遗传变异的共享和独特模式。我们观察到了位置的表型变异,并发现高血压的发生率很高,特别是在南部高地采样点,以及西海岸采样点的自我报告疟疾患病率相对其他采样点较高。在过滤到 214 名最小相关个体的子集后,我们发现了与身体成分特征相关的多个遗传关联,包括许多仅在非洲人群或来自 1000 基因组计划的具有混合非洲血统的人群中观察到的变体。这项研究强调了在基因组研究中纳入不同人群的重要性,即使是在小队列规模的情况下,也有可能获得新的见解。该项目是在马达加斯加当地利益相关者的合作和咨询下进行的,是优先考虑社区参与并可能影响我们对人类健康和疾病的理解的基因组研究的一个例子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01da/11415767/1ac2b6a4f098/gr1.jpg

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