Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
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DOI:
10.1186/s13059-022-02837-1
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发表时间:
2022-12-27
期刊:
影响因子:
12.3
通讯作者:
--
中科院分区:
生物学1区
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已知近1000个基因座中的遗传变异有助于调节血脂水平。然而,这些关联背后的生物学途径往往是未知的,这限制了对这些发现的理解,并阻碍了下游的转化工作,如药物靶点的发现。为了扩大我们对控制血脂水平的潜在生物学途径和机制的理解,我们利用一项大型的多祖先血脂meta分析(N = 1,654,960),利用六种基因预测方法对2286种血脂相关的假定因果基因进行了优先排序。使用全现象关联(PheWAS)扫描,我们确定了遗传预测的脂质水平与其他疾病和病症的关系。我们确认了已知的多效性与心血管表型的关联,并确定了新的关联,特别是与胆石症的风险。我们对脂质水平进行了性别分层的GWAS荟萃分析,结果显示3-5%的常染色体脂质相关基因座表现出性别偏倚效应。最后,我们报告了在X染色体上发现的21个新的脂质位点。许多性别偏倚的常染色体和X染色体脂质位点显示出与性激素的多效性关联,强调了激素调节在脂质代谢中的作用。综上所述,我们的研究结果为相关变异导致血脂水平改变和潜在心血管疾病风险的生物学机制提供了见解。在线版本包含补充资料,下载地址:10.1186/s13059-022-02837-1。
Genetic variants within nearly 1000 loci are known to contribute to modulation of blood lipid levels. However, the biological pathways underlying these associations are frequently unknown, limiting understanding of these findings and hindering downstream translational efforts such as drug target discovery. To expand our understanding of the underlying biological pathways and mechanisms controlling blood lipid levels, we leverage a large multi-ancestry meta-analysis (N = 1,654,960) of blood lipids to prioritize putative causal genes for 2286 lipid associations using six gene prediction approaches. Using phenome-wide association (PheWAS) scans, we identify relationships of genetically predicted lipid levels to other diseases and conditions. We confirm known pleiotropic associations with cardiovascular phenotypes and determine novel associations, notably with cholelithiasis risk. We perform sex-stratified GWAS meta-analysis of lipid levels and show that 3–5% of autosomal lipid-associated loci demonstrate sex-biased effects. Finally, we report 21 novel lipid loci identified on the X chromosome. Many of the sex-biased autosomal and X chromosome lipid loci show pleiotropic associations with sex hormones, emphasizing the role of hormone regulation in lipid metabolism. Taken together, our findings provide insights into the biological mechanisms through which associated variants lead to altered lipid levels and potentially cardiovascular disease risk. The online version contains supplementary material available at 10.1186/s13059-022-02837-1.
DOI: 10.1038/s41588-021-00852-9
发表时间: 2021-06
期刊: Nature genetics
影响因子: 30.8
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影响因子: 13.5
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通讯作者: Willer CJ
DOI: 10.2147/vhrm.s209830
发表时间: 2019-01-01
影响因子: 2.9
作者:
Artha, I. Made Junior Rina;Bhargah, Agha;Rina, I. Ketut
通讯作者: Rina, I. Ketut
DOI: 10.1038/s41588-021-00912-0
发表时间: 2021-09-01
期刊: NATURE GENETICS
影响因子: 30.8
作者:
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通讯作者: Tenesa, Albert