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通过方差数量性状基因座对维生素D的基因-环境相互作用进行表征:一项基于英国生物银行的遗传流行病学研究。

Characterization of gene-environment interactions for vitamin D through variance quantitative trait loci: a UK Biobank-based genetic epidemiology study.

作者信息

Lu Tianyuan, Zhang Wenmin, Robinson-Cohen Cassianne, Engelman Corinne D, Lu Qiongshi, de Boer Ian H, Sun Lei, Paterson Andrew D

机构信息

Department of Population Health Sciences, University of Wisconsin-Madison, Madison, WI, United States; Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI, United States; Department of Statistical Sciences, University of Toronto, Toronto, ON, Canada.

Montreal Heart Institute, Montreal, QC, Canada.

出版信息

Am J Clin Nutr. 2025 Mar;121(3):731-740. doi: 10.1016/j.ajcnut.2025.01.021. Epub 2025 Jan 23.

Abstract

BACKGROUND

Understanding gene-environment interactions associated with vitamin D status may refine nutrition and public health strategies for vitamin D deficiency. Recent methodological advances have enabled the identification of variance quantitative trait loci (vQTLs) where gene-environment interactions are enriched.

OBJECTIVES

The study aims to identify vQTLs for serum 25-hydroxy vitamin D (25OHD) concentrations and characterize potential gene-environment interactions of vQTLs.

METHODS

We conducted vQTL discovery for 25OHD using a newly developed quantile integral linear model in the UK Biobank individuals of European (N = 313,514), African (N = 7800), East Asian (N = 2146), and South Asian (N = 8771) ancestries, respectively. We tested for interactions between the identified vQTL lead variants and 18 environmental, biological, or lifestyle factors, followed by multiple sensitivity analyses.

RESULTS

We identified 19 independent vQTL lead variants (P < 5 × 10) in the European ancestry population. No vQTLs were identified in the non-European ancestry populations, likely because of limited sample sizes. A total of 32 interactions were detected with a false discovery rate <0.05. Although known gene-season of measurement interactions were confirmed, additional interactions were identified involving modifiable risk factors, including time spent outdoors and body mass index. The magnitudes of these interactions were consistent within each locus upon adjusting for the season of measurement and other covariates. We also identified a gene-sex interaction at a vQTL that implicates DHCR7. Integrating transcript- and protein-level evidence, we found that the sex-differentiated genetic associations may act through sex-biased expression of DHCR7 isoforms in skin tissues because of alternative splicing.

CONCLUSIONS

Through the lens of vQTLs, we identified additional gene-environment interactions affecting vitamin D status in addition to the season of measurement. These findings may provide new insights into the etiology of vitamin D deficiency and encourage personalized prevention and management of associated diseases for at-risk individuals.

摘要

背景

了解与维生素D状态相关的基因-环境相互作用可能会优化针对维生素D缺乏的营养和公共卫生策略。最近的方法学进展使得能够识别基因-环境相互作用富集的变异数量性状位点(vQTL)。

目的

本研究旨在识别血清25-羟基维生素D(25OHD)浓度的vQTL,并表征vQTL潜在的基因-环境相互作用。

方法

我们分别在英国生物银行中欧洲血统(N = 313,514)、非洲血统(N = 7800)、东亚血统(N = 2146)和南亚血统(N = 8771)的个体中,使用新开发的分位数积分线性模型对25OHD进行vQTL发现。我们测试了所识别的vQTL主要变异与18种环境、生物学或生活方式因素之间的相互作用,随后进行了多次敏感性分析。

结果

我们在欧洲血统人群中识别出19个独立的vQTL主要变异(P < 5×10)。在非欧洲血统人群中未识别出vQTL,可能是由于样本量有限。共检测到32种相互作用,错误发现率<0.05。虽然确认了已知的基因-测量季节相互作用,但还识别出了涉及可改变风险因素的其他相互作用,包括户外时间和体重指数。在调整测量季节和其他协变量后,每个位点内这些相互作用的大小是一致的。我们还在一个涉及DHCR7的vQTL处识别出基因-性别相互作用。整合转录水平和蛋白质水平的证据,我们发现性别差异的遗传关联可能是由于皮肤组织中DHCR7异构体的可变剪接导致的性别偏向性表达而产生的。

结论

通过vQTL的视角,我们识别出除测量季节外影响维生素D状态的其他基因-环境相互作用。这些发现可能为维生素D缺乏的病因提供新的见解,并鼓励对高危个体进行相关疾病的个性化预防和管理。

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