Pulse Brain · Growing Health Evidence Index
Tier 3 — Observational / field trialPeer-reviewed

Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration

Joana Revez, Tian Lin, Zhen Qiao, Angli Xue, Yan Holtz, Zhihong Zhu, Jian Zeng, Huanwei Wang, Julia Sidorenko, Kathryn E. Kemper, Anna A. E. Vinkhuyzen, Julanne Frater, Darryl W. Eyles, Thomas H.J. Burne, Brittany L. Mitchell, Nicholas G. Martin, Gu Zhu, Peter M. Visscher, Jian Yang, Naomi R. Wray, John J. McGrath

Nature Communications · 2020

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Summary

This large genome-wide association study in 417,580 Europeans identified 143 genetic loci influencing 25-hydroxyvitamin D concentration, implicating biological pathways including lipid metabolism, dermal properties, and vitamin D metabolite conjugation. Mendelian randomisation analysis found no robust evidence that vitamin D status causally influences common health phenotypes (BMI, psychiatric disorders), but instead detected that many phenotypes have causal effects on vitamin D concentrations, suggesting reverse causality in observational associations.

UK applicability

The findings are directly applicable to UK populations given the ancestry composition of the study sample. The results may inform interpretation of observational associations between vitamin D status and health outcomes in UK clinical and epidemiological contexts, suggesting that health conditions may influence vitamin D metabolism rather than vice versa.

Key measures

25-hydroxyvitamin D (25OHD) concentration; 143 independent loci in 112 1-Mb regions; causal effects estimated via Mendelian randomisation models

Outcomes reported

The study identified 143 independent genetic loci associated with 25-hydroxyvitamin D concentration in a large European population sample. Mendelian randomisation analysis examined the causal relationships between vitamin D status and various health phenotypes including BMI and psychiatric disorders.

Theme
Nutrition & health
Subject
Micronutrients & dietary adequacy
Study type
Research
Study design
Genome-wide association study with Mendelian randomisation analysis
Source type
Peer-reviewed study
Status
Published
Geography
Europe
System type
Human clinical
DOI
10.1038/s41467-020-15421-7
Catalogue ID
SNmohdwgm4-eeywsa

Topic tags

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