Evidence map›Paper›PMID 38451975›Full record

ArticlePloS one2024

The relationship between emotional disorders and heart rate variability: A Mendelian randomization study.

Xu Luo, Rui Wang, YunXiang Zhou, Wen Xie

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xu LuoCollege of Clinical Medicine, University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Rui WangCollege of Clinical Medicine, University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
YunXiang ZhouCollege of Clinical Medicine, University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Wen XieCollege of Clinical Medicine, University of Traditional Chinese Medicine, Chengdu, Sichuan, China.ORCID 0009-0003-6198-4293

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePrevious studies have shown that emotional disorders are negatively associated with heart rate variability (HRV), but the potential causal relationship between genetic susceptibility to emotional disorders and HRV remains unclear. We aimed to perform a Mendelian randomization (MR) study to investigate the potential association between emotional disorders and HRV.

methodsThe data used for this study were obtained from publicly available genome-wide association study datasets. Five models, including the inverse variance weighted model (IVW), the weighted median estimation model (WME), the weighted model-based method (WM), the simple model (SM) and the MR-Egger regression model (MER), were utilized for MR. The leave-one-out sensitivity test, MR pleiotropy residual sum and outlier test (MR-PRESSO) and Cochran's Q test were used to confirm heterogeneity and pleiotropy.

resultsMR analysis revealed that genetic susceptibility to broad depression was negatively correlated with HRV (pvRSA/HF) (OR = 0.380, 95% CI 0.146-0.992; p = 0.048). However, genetic susceptibility to irritability was positively correlated with HRV (pvRSA/HF, SDNN) (OR = 2.017, 95% CI 1.152-3.534, p = 0.008) (OR = 1.154, 95% CI 1.000-1.331, p = 0.044). Genetic susceptibility to anxiety was positively correlated with HRV (RMSSD) (OR = 2.106, 95% CI 1.032-4.299; p = 0.041). No significant directional pleiotropy or heterogeneity was detected. The accuracy and robustness of these findings were confirmed through a sensitivity analysis.

conclusionsOur MR study provides genetic support for the causal effects of broad depression, irritable mood, and anxiety on HRV.

Indexed as

Genome-Wide Association StudyMendelian Randomization AnalysisAnxietyGenetic Predisposition to DiseaseHeart RateHumans

Identifiers

PMID38451975
PMCPMC10919610

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