Evidence map›Paper›PMID 41458058›Full record

ArticleGlobal heart2025

Association of Female Reproductive Factors with Incident Cardiometabolic Disease: Finding from a European Population-Based Study.

Changxi Wang, Zhijie Lin, Fan Chen, Xiaoqian Zhu, Weize Lin, Ziqing Ruan, Jiabin Tu, Kaiyang Lin, Yansong Guo

Abstract read
In one paragraph

Article in Global heart, 2025. 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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0cells of the map it votes in
0citing 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.

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

The trial behind it

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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

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

9 authors.

Changxi Wang *Department of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Zhijie Lin *Department of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.ORCID 0009-0002-1849-3926
Fan Chen *Department of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Xiaoqian ZhuDepartment of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Weize LinDepartment of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Ziqing RuanDepartment of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Jiabin TuDepartment of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Kaiyang LinDepartment of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Yansong GuoDepartment of Cardiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.ORCID 0000-0001-6607-6938

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cardiometabolic diseases (CMD), including ischemic heart disease, stroke, and type 2 diabetes, have caused an enormous global healthcare burden. Beyond traditional risk factors, female reproductive factors may also be associated with CMD. However, comprehensive evaluations of female reproductive factors related CMD is limited. Methods: A total of 189,411 women with no prior CMD from the UK Biobank cohort from 2007 to 2010 were included and followed until December 2022. Associations between reproductive factors and CMD were analyzed using Cox proportional hazards models with adjustment for potential confounders based on the directed acyclic graph (DAG). Results: During a median follow-up of 13.2 years, 17,251 incident CMD events occurred. Compared to menarche at age 12-13 years, <12 years and >13 years had a higher risk of CMD (HR <12 year (y) vs 12-13 y: 1.04 [95% CI, 1.01-1.08]; >13 y vs 12-13 y: 1.08 [1.04-1.13]). Earlier age at menopause was related to a higher risk of CMD (HR <46 y vs 50-51 y: 1.22 [1.15-1.29]; 46-49 y vs 50-51 y: 1.08 [1.03-1.14]), and a short reproductive lifespan (HR <33 y vs 36-38 y: 1.19 [1.13-1.25]; 33-35 y vs 36-38 y: 1.08 [1.03-1.14]). Younger age at first live birth (HR <22 y vs 24-26 y: 1.18 [1.12-1.24]; 22-23 y vs 24-26 y: 1.06 [1.00-1.12]) and last live birth (HR <26 y vs 29-30 y: 1.12 [1.06-1.18]) were associated with higher risk. Women with three or four children (HR 3-4 children: 1.21 [1.15-1.28]) and those with more than four children (HR >4 children: 1.27 [1.07-1.52]) were associated with higher risk of CMD. Recurrent pregnancy loss was associated with a 39% and 14% higher risk of CMD, respectively. Conclusion: Female reproductive factors are associated with CMD, independent of traditional risk factors. These reproductive factors could inform clinical screening and improve cardiometabolic risk assessment in women.

Indexed as

Cardiovascular DiseasesReproductive HistoryAdolescentAdultChildEuropeFemaleFollow-Up StudiesHumansIncidenceMenarcheMenopauseMiddle AgedRisk AssessmentRisk FactorsYoung Adultcardiometabolic diseasefemale reproductive factorsmetabolic healthreproductive health

Identifiers

PMID41458058
PMCPMC12742377

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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.