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肥胖与 2 型糖尿病遗传不一致的全表型比较分析。

A phenome-wide comparative analysis of genetic discordance between obesity and type 2 diabetes.

机构信息

Genetic and Molecular Epidemiology Unit, Lund University Diabetes Centre, Department of Clinical Science, Lund University, Skåne University Hospital, Malmö, Sweden.

Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, UK.

出版信息

Nat Metab. 2023 Feb;5(2):237-247. doi: 10.1038/s42255-022-00731-5. Epub 2023 Jan 26.


DOI:10.1038/s42255-022-00731-5
PMID:36703017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9970876/
Abstract

Obesity and type 2 diabetes are causally related, yet there is considerable heterogeneity in the consequences of both conditions and the mechanisms of action are poorly defined. Here we show a genetic-driven approach defining two obesity profiles that convey highly concordant and discordant diabetogenic effects. We annotate and then compare association signals for these profiles across clinical and molecular phenotypic layers. Key differences are identified in a wide range of traits, including cardiovascular mortality, fat distribution, liver metabolism, blood pressure, specific lipid fractions and blood levels of proteins involved in extracellular matrix remodelling. We find marginal differences in abundance of Bacteroidetes and Firmicutes bacteria in the gut. Instrumental analyses reveal prominent causal roles for waist-to-hip ratio, blood pressure and cholesterol content of high-density lipoprotein particles in the development of diabetes in obesity. We prioritize 17 genes from the discordant signature that convey protection against type 2 diabetes in obesity, which may represent logical targets for precision medicine approaches.

摘要

肥胖症和 2 型糖尿病存在因果关系,但这两种病症的后果存在很大差异,其作用机制也尚未明确。在这里,我们通过遗传驱动的方法定义了两种肥胖表型,它们具有高度一致和不一致的致糖尿病作用。我们对这些表型进行注释,然后比较它们在临床和分子表型层面的关联信号。在包括心血管死亡率、脂肪分布、肝脏代谢、血压、特定脂质分数以及参与细胞外基质重塑的蛋白质的血液水平在内的广泛特征中,我们发现了关键的差异。我们还在肠道中发现了拟杆菌门和厚壁菌门细菌丰度的微小差异。工具分析表明,腰臀比、血压和高密度脂蛋白颗粒中的胆固醇含量在肥胖症中导致 2 型糖尿病的发展中起着重要的因果作用。我们从不一致的特征中确定了 17 个基因,这些基因在肥胖症中对 2 型糖尿病具有保护作用,它们可能是精准医学方法的合理目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/59c181218a22/42255_2022_731_Fig6_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/221f9f4db2f9/42255_2022_731_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/451485e7ef85/42255_2022_731_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/d38ba5fcfde3/42255_2022_731_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/13b2d56c9573/42255_2022_731_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/ccc5d13f2d57/42255_2022_731_Fig5_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/59c181218a22/42255_2022_731_Fig6_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/221f9f4db2f9/42255_2022_731_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/451485e7ef85/42255_2022_731_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/d38ba5fcfde3/42255_2022_731_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/13b2d56c9573/42255_2022_731_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/ccc5d13f2d57/42255_2022_731_Fig5_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e6/9970876/59c181218a22/42255_2022_731_Fig6_ESM.jpg

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本文引用的文献

[1]
Independent phenotypic plasticity axes define distinct obesity sub-types.

Nat Metab. 2022-9

[2]
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.

Nat Genet. 2021-9

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Cardiovasc Drugs Ther. 2021-12

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Nat Metab. 2021-2

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Nat Genet. 2021-2

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Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease.

Genome Med. 2021-1-13

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Nucleic Acids Res. 2021-1-8

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Am J Hum Genet. 2020-12-3

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Nucleic Acids Res. 2021-1-8

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