Evidence map›Paper›PMID 36266699›Full record

ArticleJournal of translational medicine2022

Causality of genetically determined metabolites on anxiety disorders: a two-sample Mendelian randomization study.

Gui Xiao, Qingnan He, Li Liu, Tingting Zhang, Mengjia Zhou, Xingxing Li, Yijun Chen, Yanyi Chen, Chunxiang Qin

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Article in Journal of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 6 pooled it
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

97 citing papers in PubMed, 6 syntheses or guidelines pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Gui XiaoDepartment of Health Management, The Third Xiangya Hospital, Central South University, Changsha, China.
Qingnan HeThe Third Xiangya Hospital, Central South University, Changsha, China.
Li LiuDepartment of Health Management, The Third Xiangya Hospital, Central South University, Changsha, China.
Tingting ZhangDepartment of Health Management, The Third Xiangya Hospital, Central South University, Changsha, China.
Mengjia ZhouDepartment of Health Management, The Third Xiangya Hospital, Central South University, Changsha, China.
Xingxing LiDepartment of Health Management, The Third Xiangya Hospital, Central South University, Changsha, China.
Yijun ChenXiangya Medicine School, Central South University, Changsha, China.
Yanyi ChenXiangya Medicine School, Central South University, Changsha, China.
Chunxiang QinDepartment of Health Management, The Third Xiangya Hospital, Central South University, Changsha, China. Chunxiangqin@csu.edu.cn.ORCID 0000-0002-4889-1696

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough anxiety disorders are one of the most prevalent mental disorders, their underlying biological mechanisms have not yet been fully elucidated. In recent years, genetically determined metabolites (GDMs) have been used to reveal the biological mechanisms of mental disorders. However, this strategy has not been applied to anxiety disorders. Herein, we explored the causality of GDMs on anxiety disorders through Mendelian randomization study, with the overarching goal of unraveling the biological mechanisms.

methodsA two-sample Mendelian randomization (MR) analysis was implemented to assess the causality of GDMs on anxiety disorders. A genome-wide association study (GWAS) of 486 metabolites was used as the exposure, whereas four different GWAS datasets of anxiety disorders were the outcomes. Notably, all datasets were acquired from publicly available databases. A genetic instrumental variable (IV) was used to explore the causality between the metabolite and anxiety disorders for each metabolite. The MR Steiger filtering method was implemented to examine the causality between metabolites and anxiety disorders. The standard inverse variance weighted (IVW) method was first used for the causality analysis, followed by three additional MR methods (the MR-Egger, weighted median, and MR-PRESSO (pleiotropy residual sum and outlier) methods) for sensitivity analyses in MR analysis. MR-Egger intercept, and Cochran's Q statistical analysis were used to evaluate possible heterogeneity and pleiotropy. Bonferroni correction was used to determine the causative association features (P < 1.03 × 10

resultsIn MR analysis, 85 significant causative relationship GDMs were identified. Among them, 11 metabolites were overlapped in the four different datasets of anxiety disorders. Bonferroni correction showing1-linoleoylglycerophosphoethanolamine (OR

conclusionThis study provides new insights into the causal effects of GDMs on anxiety disorders by integrating genomics and metabolomics. The metabolites that drive anxiety disorders may be suited to serve as biomarkers and also will help to unravel the biological mechanisms of anxiety disorders.

Indexed as

Genome-Wide Association StudyMendelian Randomization AnalysisAnxiety DisordersBile Acids and SaltsHumansIsoleucineLeucinePolymorphism, Single NucleotideValineBile Acids and SaltsIsoleucineLeucineValine1-linoleoylglycerophosphoethanolamineAnxiety disordersGenetically determined metabolitesMendelian randomizationSerum metabolite

Identifiers

PMID36266699
PMCPMC9583573

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.