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鉴定不同种族和民族人群中与 2 型糖尿病风险相关的蛋白质。

Identification of proteins associated with type 2 diabetes risk in diverse racial and ethnic populations.

机构信息

Cancer Epidemiology Division, Population Sciences in the Pacific Program, University of Hawai'i Cancer Center, University of Hawai'i at Mānoa, Honolulu, HI, USA.

Department of Quantitative Health Sciences, John A. Burns School of Medicine, University of Hawai'i at Mānoa, Honolulu, HI, USA.

出版信息

Diabetologia. 2024 Dec;67(12):2754-2770. doi: 10.1007/s00125-024-06277-3. Epub 2024 Sep 30.

Abstract

AIMS/HYPOTHESIS: Several studies have reported associations between specific proteins and type 2 diabetes risk in European populations. To better understand the role played by proteins in type 2 diabetes aetiology across diverse populations, we conducted a large proteome-wide association study using genetic instruments across four racial and ethnic groups: African; Asian; Hispanic/Latino; and European.

METHODS

Genome and plasma proteome data from the Multi-Ethnic Study of Atherosclerosis (MESA) study involving 182 African, 69 Asian, 284 Hispanic/Latino and 409 European individuals residing in the USA were used to establish protein prediction models by using potentially associated cis- and trans-SNPs. The models were applied to genome-wide association study summary statistics of 250,127 type 2 diabetes cases and 1,222,941 controls from different racial and ethnic populations.

RESULTS

We identified three, 44 and one protein associated with type 2 diabetes risk in Asian, European and Hispanic/Latino populations, respectively. Meta-analysis identified 40 proteins associated with type 2 diabetes risk across the populations, including well-established as well as novel proteins not yet implicated in type 2 diabetes development.

CONCLUSIONS/INTERPRETATION: Our study improves our understanding of the aetiology of type 2 diabetes in diverse populations.

DATA AVAILABILITY

The summary statistics of multi-ethnic type 2 diabetes GWAS of MVP, DIAMANTE, Biobank Japan and other studies are available from The database of Genotypes and Phenotypes (dbGaP) under accession number phs001672.v3.p1. MESA genetic, proteome and covariate data can be accessed through dbGaP under phs000209.v13.p3. All code is available on GitHub ( https://github.com/Arthur1021/MESA-1K-PWAS ).

摘要

目的/假设:几项研究报告了特定蛋白质与欧洲人群 2 型糖尿病风险之间的关联。为了更好地了解蛋白质在不同人群 2 型糖尿病发病机制中的作用,我们使用四个种族和族裔群体(非洲裔、亚洲裔、西班牙裔/拉丁裔和欧洲裔)的全基因组关联研究中的遗传工具进行了大规模的蛋白质组全基因组关联研究。

方法

使用美国多民族动脉粥样硬化研究(MESA)研究中的全基因组和血浆蛋白质组数据,涉及 182 名非洲人、69 名亚洲人、284 名西班牙裔/拉丁裔和 409 名欧洲人,通过使用潜在相关的顺式和反式单核苷酸多态性建立蛋白质预测模型。将这些模型应用于来自不同种族和族裔人群的 250127 例 2 型糖尿病病例和 1222941 例对照的全基因组关联研究汇总统计数据。

结果

我们分别在亚洲、欧洲和西班牙裔/拉丁裔人群中鉴定出三个、四个和一个与 2 型糖尿病风险相关的蛋白质。荟萃分析确定了 40 个与多种人群 2 型糖尿病风险相关的蛋白质,包括已确立的和尚未涉及 2 型糖尿病发病机制的新型蛋白质。

结论/解释:我们的研究提高了我们对不同人群 2 型糖尿病发病机制的理解。

数据可用性

MVP、DIAMANTE、日本生物银行和其他研究的多民族 2 型糖尿病 GWAS 的汇总统计数据可从基因型和表型数据库(dbGaP)中获得,访问号为 phs001672.v3.p1。MESA 遗传、蛋白质组和协变量数据可通过 dbGaP 访问,访问号为 phs000209.v13.p3。所有代码都可在 GitHub 上获得(https://github.com/Arthur1021/MESA-1K-PWAS)。

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