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Causal associations between risk factors and common diseases inferred from GWAS summary data.

作者信息

Zhu Zhihong, Zheng Zhili, Zhang Futao, Wu Yang, Trzaskowski Maciej, Maier Robert, Robinson Matthew R, McGrath John J, Visscher Peter M, Wray Naomi R, Yang Jian

机构信息

Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.

The Eye Hospital, School of Ophthalmology & Optometry, Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China.

出版信息

Nat Commun. 2018 Jan 15;9(1):224. doi: 10.1038/s41467-017-02317-2.


DOI:10.1038/s41467-017-02317-2
PMID:29335400
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5768719/
Abstract

Health risk factors such as body mass index (BMI) and serum cholesterol are associated with many common diseases. It often remains unclear whether the risk factors are cause or consequence of disease, or whether the associations are the result of confounding. We develop and apply a method (called GSMR) that performs a multi-SNP Mendelian randomization analysis using summary-level data from genome-wide association studies to test the causal associations of BMI, waist-to-hip ratio, serum cholesterols, blood pressures, height, and years of schooling (EduYears) with common diseases (sample sizes of up to 405,072). We identify a number of causal associations including a protective effect of LDL-cholesterol against type-2 diabetes (T2D) that might explain the side effects of statins on T2D, a protective effect of EduYears against Alzheimer's disease, and bidirectional associations with opposite effects (e.g., higher BMI increases the risk of T2D but the effect of T2D on BMI is negative).

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/072ffba30f21/41467_2017_2317_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/c0c1c3e418bf/41467_2017_2317_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/b969095d8f49/41467_2017_2317_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/aad13bee467b/41467_2017_2317_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/535dfd7cd626/41467_2017_2317_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/fddd615abeab/41467_2017_2317_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/072ffba30f21/41467_2017_2317_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/c0c1c3e418bf/41467_2017_2317_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/b969095d8f49/41467_2017_2317_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/aad13bee467b/41467_2017_2317_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/535dfd7cd626/41467_2017_2317_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/fddd615abeab/41467_2017_2317_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/5768719/072ffba30f21/41467_2017_2317_Fig6_HTML.jpg

相似文献

[1]
Causal associations between risk factors and common diseases inferred from GWAS summary data.

Nat Commun. 2018-1-15

[2]
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[3]
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[6]
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[7]
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Mol Genet Genomics. 2025-8-31

[2]
Trans-eQTLs Can Be Used to Identify Tissue-Specific Gene Regulatory Networks.

Curr Issues Mol Biol. 2025-7-29

[3]
Dissecting causal relationships between cortical morphology and neuropsychiatric disorders: a bidirectional Mendelian randomization study.

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[4]
Shared genetic susceptibility between idiopathic inflammatory myopathies and common B cell lymphoma subtypes found primarily in the human leucocyte antigen region.

RMD Open. 2025-8-25

[5]
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking.

Nat Commun. 2025-8-23

[6]
The proteogenomic landscape of the human kidney and implications for cardio-kidney-metabolic health.

Nat Med. 2025-8-12

[7]
Iron Homeostasis as a Mediator Linking Central Obesity with MASLD and Primary Liver Cancer: A Two-Step Mendelian Randomization Study.

Biomedicines. 2025-7-4

[8]
Placental Gene Expression Associated With Early Childhood Growth Trajectories and Obesity Risk.

Obesity (Silver Spring). 2025-7-25

[9]
Using Mendelian randomization analyses in osteoarthritis: state of art and future perspectives.

Ann Med. 2025-12

[10]
Causal effects of antibody-mediated immune responses on myocarditis: A two-sample Mendelian randomization study.

Medicine (Baltimore). 2025-7-18

本文引用的文献

[1]
Mendelian Randomization Implicates High-Density Lipoprotein Cholesterol-Associated Mechanisms in Etiology of Age-Related Macular Degeneration.

Ophthalmology. 2017-8

[2]
Epidemiology of age-related macular degeneration (AMD): associations with cardiovascular disease phenotypes and lipid factors.

Eye Vis (Lond). 2016-12-22

[3]
Sensitivity Analyses for Robust Causal Inference from Mendelian Randomization Analyses with Multiple Genetic Variants.

Epidemiology. 2017-1

[4]
A plethora of pleiotropy across complex traits.

Nat Genet. 2016-6-28

[5]
Genome-wide association study identifies 74 loci associated with educational attainment.

Nature. 2016-5-26

[6]
Detection and interpretation of shared genetic influences on 42 human traits.

Nat Genet. 2016-7

[7]
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets.

Nat Genet. 2016-3-28

[8]
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.

Nat Genet. 2016-2

[9]
Combining information on multiple instrumental variables in Mendelian randomization: comparison of allele score and summarized data methods.

Stat Med. 2016-5-20

[10]
An atlas of genetic correlations across human diseases and traits.

Nat Genet. 2015-11

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