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利用哮喘遗传风险评分揭示多基因多效性。

Revealing polygenic pleiotropy using genetic risk scores for asthma.

机构信息

Department of Human Genetics, University of Chicago, Chicago, IL, USA.

Biological Sciences Collegiate Division, University of Chicago, Chicago, IL, USA.

出版信息

HGG Adv. 2023 Aug 17;4(4):100233. doi: 10.1016/j.xhgg.2023.100233. eCollection 2023 Oct 12.

Abstract

In this study we examined how genetic risk for asthma associates with different features of the disease and with other medical conditions and traits. Using summary statistics from two multi-ancestry genome-wide association studies of asthma, we modeled polygenic risk scores (PRSs) and validated their predictive performance in the UK Biobank. We then performed phenome-wide association studies of the asthma PRSs with 371 heritable traits in the UK Biobank. We identified 228 total significant associations across a variety of organ systems, including associations that varied by PRS model, sex, age of asthma onset, ancestry, and human leukocyte antigen region alleles. Our results highlight pervasive pleiotropy between asthma and numerous other traits and conditions and elucidate pathways that contribute to asthma and its comorbidities.

摘要

在这项研究中,我们研究了哮喘的遗传风险如何与疾病的不同特征以及其他医疗状况和特征相关。我们使用来自两项哮喘多血统全基因组关联研究的汇总统计数据,对多基因风险评分(PRS)进行建模,并在英国生物库中验证其预测性能。然后,我们对英国生物库中与 371 种可遗传特征相关的哮喘 PRS 进行了全表型关联研究。我们在各种器官系统中发现了 228 个总显著关联,包括与 PRS 模型、性别、哮喘发病年龄、祖源和人类白细胞抗原区域等位基因不同的关联。我们的研究结果强调了哮喘与许多其他特征和状况之间普遍存在的多效性,并阐明了导致哮喘及其合并症的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cca/10474095/dd11c4e72ac0/gr1.jpg

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