Evidence map›Paper›PMID 41462452›Full record

ArticleBMC medicine2025

Systolic and diastolic blood pressure, abdominal obesity, and alcohol consumption contribute to the risk of hypertrophic and dilated cardiomyopathies in European and East Asian populations.

Wenqiang Zhang, Lingli Qiu, Zhiwen Cao, Jinyan Xie, Jiejing Jin, Ruru Bai, Jiajia Xiang, Yeqing Zou, Xiaogang Peng, Rong Wan and 2 more

Abstract read
In one paragraph

Article in BMC medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Wenqiang ZhangJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China. zwqscu@126.com.
Lingli QiuDepartment of Epidemiology and Biostatistics, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, China.
Zhiwen CaoJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Jinyan XieJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Jiejing JinJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Ruru BaiJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Jiajia XiangJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Yeqing ZouJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Xiaogang PengJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Rong WanJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Yang ShenJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China. sain.yong@gmail.com.
Kui HongJiangxi Provincial Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.

Funding

Jiangxi Province Key Laboratory of Molecular Medicine No.2024SSY06231Jiangxi Provincial Natural Science Foundation 20223BBG71011Jiangxi Provincial Natural Science Foundation 20232BAB216014, 20242BAB25435Jiangxi Provincial Natural Science Foundation No. 20252BAC200135National Natural Science Foundation Incubation Project of the Second Affiliated Hospital of Nanchang University 2024YNFY12012National Natural Science Foundation of China 82360048Science and Technology Plan Project of Jiangxi Province Health Commission 202510042
6 · The paper itself

Abstract

backgroundPotentially modifiable cardiovascular risk factors, including hypertension, diabetes, obesity, alcohol consumption, and smoking initiation, are associated with hypertrophic (HCM) and dilated (DCM) cardiomyopathies, representing promising targets for interventions. However, the causality and cross-ancestry generalizability of these associations remain uncertain.

methodsCollecting summary-level data from genome-wide association studies for systolic (SBP) and diastolic (DBP) blood pressure, hypertension, type 2 diabetes, fasting glucose, glycated hemoglobin, body mass index (BMI), waist circumference (WC), alcohol consumption, smoking initiation, HCM, and DCM (sample size ranging from 38,288 to 1,812,017), we performed comprehensive two-sample univariable Mendelian randomization (MR) to evaluate the causal effect of each trait on HCM and DCM in both European and East Asian populations. We performed multivariable MR to investigate the independent effects of interrelated traits (SBP vs. DBP; BMI vs. WC).

resultsMR analyses identified reliable evidence of a causal effect of SBP on HCM (Europeans: odds ratio (OR) = 1.03, 95% confidence interval (CI) = 1.02-1.04; East Asians: OR = 1.06, 95% CI = 1.03-1.08). For DCM, reliable evidence of causal effects was identified for DBP (Europeans: OR = 1.04, 95% CI = 1.03-1.04; East Asians: OR = 1.07, 95% CI = 1.04-1.11), WC (Europeans: OR = 1.73, 95% CI = 1.58-1.89; East Asians: OR = 3.32, 95% CI = 1.22-9.03), and alcohol consumption (Europeans: OR = 1.50, 95% CI = 1.20-1.86; East Asians: OR = 1.32, 95% CI = 1.11-1.56). In Europeans, genetically predicted higher WC (OR = 1.75, 95% CI = 1.53-2.01) and smoking initiation (OR = 1.34, 95% CI = 1.16-1.56) specifically increased the risk of HCM and DCM, respectively, while genetically predicted higher alcohol consumption (OR = 1.68, 95% CI = 1.36-2.07) specifically increased the risk of HCM in East Asians.

conclusionsThis study provided reliable cross-ancestry genetic evidence supporting higher SBP as a causal risk factor for HCM and higher DBP, WC, and alcohol consumption as causal risk factors for DCM. These findings underscore the potential of precision prevention strategies targeting modifiable cardiovascular risk factors to reduce cardiomyopathy burden across populations.

Indexed as

Alcohol DrinkingBlood PressureCardiomyopathy, DilatedCardiomyopathy, HypertrophicObesity, AbdominalEast Asian PeopleEuropeFemaleGenome-Wide Association StudyHumansMaleMendelian Randomization AnalysisRisk FactorsWhite PeopleCausalityDilated cardiomyopathyHypertrophic cardiomyopathyMendelian randomizationModifiable cardiovascular risk factors

Identifiers

PMID41462452
PMCPMC12751570

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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.