Evidence map›Paper›PMID 42026604›Full record

ArticleBMC medicine2026

Adulthood stressful life events as predictors of incident cardiovascular disease: insights from two prospective cohorts.

Shuang Wu, Siqi Lyu, Yimeng Wang, Hanyang Liang, Wei Xu, Juan Wang, Xinghui Shao, Han Zhang, Hongyu Liu, Bi Huang and 2 more

Abstract read
In one paragraph

Article in BMC medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Shuang Wu *National Center for Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Siqi Lyu *National Center for Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Yimeng WangNational Center for Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Hanyang LiangNational Center for Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Wei XuNational Center for Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Juan WangNational Center for Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Xinghui ShaoNational Center for Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Han ZhangNational Center for Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Hongyu LiuLiverpool Centre for Cardiovascular Science, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, William Henry Duncan Building, 6 West Derby Street, Liverpool, L7 8TX, UK.
Bi HuangDepartment of Cardiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, People's Republic of China.
Yang ChenLiverpool Centre for Cardiovascular Science, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, William Henry Duncan Building, 6 West Derby Street, Liverpool, L7 8TX, UK. yang.chen2@liverpool.ac.uk.
Gregory Y H LipLiverpool Centre for Cardiovascular Science, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, William Henry Duncan Building, 6 West Derby Street, Liverpool, L7 8TX, UK. gregory.lip@liverpool.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStressful life events (SLEs) in adulthood are potential risk factors for cardiovascular disease (CVD), yet evidence remains inconsistent. This study examined the association between adulthood SLEs and incident CVD and evaluated mediation by depression, physical inactivity, and smoking.

methodsWe analyzed harmonized data from two nationally representative aging cohorts: the US Health and Retirement Study and the English Longitudinal Study of Ageing. SLEs were assessed at baseline, and incident CVD was physician-diagnosed. We used Cox and restricted mean survival time (RMST) regression to estimate hazard ratios (HRs) and RMST differences, set at the time point when 90% of incident CVD events had accrued (7.8 years). Population attributable fractions (PAFs) based on RMST and mediation analyses via RMST pseudo-value regression quantified contributions of SLEs and behavioral pathways.

resultsAmong 18,898 participants without baseline cardiovascular disease (mean age 64.5 years; 39.8% male), 2,782 incident CVD cases were documented (incidence rate: 2.51 per 100 person-years). RMST analysis showed that any SLE exposure was related to significant reductions in event-free survival, including a 2.22-month decrease for CVD (95% CI: -2.90 to -1.53), a 1.57-month decrease for heart disease (95% CI: -2.16 to -0.99), and a 0.79-month decrease for stroke (95% CI: -1.16 to -0.41), with a clear dose-response relationship. Corresponding Cox proportional hazards models showed adjusted HRs of 1.20 (95% CI: 1.11–1.30) for CVD, 1.16 (95% CI: 1.07–1.27) for heart disease, and 1.26 (95% CI: 1.09–1.46) for stroke. Each additional SLE increased CVD, heart disease, and stroke risks by 11%, 10%, and 11%. PAFs attributable to SLEs exposure were 2.6% for CVD, 1.7% for heart disease, and 0.8% for stroke. Mediation analyses revealed that depression, physical inactivity, and current smoking accounted for 7.2%, 4.5%, and 4.5% of the total effect of SLEs on CVD, respectively.

conclusionsAdulthood SLEs are independently associated with increased CVD risk, with depression, physical inactivity, and smoking explaining a modest proportion of this association.

Indexed as

Cardiovascular DiseasesLife Change EventsStress, PsychologicalAgedDepressionFemaleHumansIncidenceLongitudinal StudiesMaleMiddle AgedProspective StudiesRisk FactorsSmokingUnited Statescardiovascular diseaseheart diseasemediation analysispopulation-attributable fractionstressful life eventsstroke

Identifiers

PMID42026604
PMCPMC13244983

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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.