Evidence map›Paper›PMID 32563191›Full record

ArticleHuman reproduction (Oxford, England)2020

Type of menopause, age of menopause and variations in the risk of incident cardiovascular disease: pooled analysis of individual data from 10 international studies.

Dongshan Zhu, Hsin-Fang Chung, Annette J Dobson, Nirmala Pandeya, Eric J Brunner, Diana Kuh, Darren C Greenwood, Rebecca Hardy, Janet E Cade, Graham G Giles and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Human reproduction (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 4 pooled it
9.8field-weighted citation impact, top 1% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

61 citing papers in PubMed, 4 syntheses or guidelines pooled it, 123 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Neurologic Complications of Pregnancy and Menopause.Continuum (Minneapolis, Minn.) · 2026
    Review
  18. Article
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

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

16 authors at 8 institutions in 6 countries.

Dongshan ZhuThe University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.
Hsin-Fang ChungThe University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.
Annette J DobsonThe University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.
Nirmala PandeyaThe University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.
Eric J BrunnerDepartment of Epidemiology and Public Health, University College London, London, UK.
Diana KuhMedical Research Council Unit for Lifelong Health and Ageing at UCL, London, UK.
Darren C GreenwoodNutritional Epidemiology Group, School of Food Science and Nutrition, University of Leeds, Leeds, UK.
Rebecca HardyCLOSER, UCL Institute of Education, London, UK.
Janet E CadeNutritional Epidemiology Group, School of Food Science and Nutrition, University of Leeds, Leeds, UK.
Graham G GilesCancer Epidemiology Division, Cancer Council Victoria, Melbourne, Victoria, Australia.
Fiona BruinsmaCancer Epidemiology Division, Cancer Council Victoria, Melbourne, Victoria, Australia.
Panayotes DemakakosDepartment of Epidemiology and Public Health, University College London, London, UK.
Mette Kildevæld SimonsenUcDiakonissen and Parker Institute, Frederiksberg, Denmark.
Sven SandinDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Elisabete WeiderpassInternational Agency for Research on Cancer, World Health Organisation, Lyon, France.
Gita D MishraThe University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.
University of Queensland · AUUniversity College London · GBCancer Council Victoria · AUUniversity of Leeds · GBCentre International de Recherche sur le Cancer · FRFrederiksberg Hospital · DKIcahn School of Medicine at Mount Sinai · USMRC Unit for Lifelong Health and Ageing · GB

Funding

Project-001R01AG017644 · NIA · UNIVERSITY OF LONDON INST OF NEUROLOGY · PI Andrew Steptoe · 2000 to 2026
$56.2M
British Heart Foundation RG/13/2/30098British Heart Foundation RG/16/11/32334Medical Research Council K013351Medical Research Council MC UU 12019/1NIA NIH HHS R01 AG017644World Health Organization 001
6 · The paper itself

Abstract

study questionHow does the risk of cardiovascular disease (CVD) vary with type and age of menopause? SUMMARY ANSWER: Earlier surgical menopause (e.g. <45 years) poses additional increased risk of incident CVD events, compared to women with natural menopause at the same age, and HRT use reduced the risk of CVD in women with early surgical menopause. WHAT IS KNOWN ALREADY: Earlier age at menopause has been linked to an increased risk of CVD mortality and all-cause mortality, but the extent that this risk of CVD varies by type of menopause and the role of postmenopausal HRT use in reducing this risk is unclear. STUDY DESIGN, SIZE, DURATION: Pooled individual-level data of 203 767 postmenopausal women from 10 observational studies that contribute to the International collaboration for a Life course Approach to reproductive health and Chronic disease Events (InterLACE) consortium were included in the analysis. PARTICIPANTS/MATERIALS, SETTING,

methodsPostmenopausal women who had reported menopause (type and age of menopause) and information on non-fatal CVD events were included. Type of menopause (natural menopause and surgical menopause) and age at menopause (categorised as <35, 35-39, 40-44, 45-49, 50-54 and ≥55 years) were exposures of interest. Natural menopause was defined as absence of menstruation over a period of 12 months (no hysterectomy and/or oophorectomy) and surgical menopause as removal of both ovaries. The study outcome was the first non-fatal CVD (defined as either incident coronary heart disease (CHD) or stroke) event ascertained from hospital medical records or self-reported. We used Cox proportional hazards models to estimate hazard ratios (HRs) and 95% CI for non-fatal CVD events associated with natural menopause and surgical menopause. MAIN RESULTS AND THE ROLE OF CHANCE: Compared with natural menopause, surgical menopause was associated with over 20% higher risk of CVD (HR 1.22, 95% CI 1.16-1.28). After the stratified analysis by age at menopause, a graded relationship for incident CVD was observed with lower age at menopause in both types of natural and surgical menopause. There was also a significant interaction between type of menopause and age at menopause (P < 0.001). Compared with natural menopause at 50-54 years, women with surgical menopause before 35 (2.55, 2.22-2.94) and 35-39 years (1.91, 1.71-2.14) had higher risk of CVD than those with natural menopause (1.59, 1.23-2.05 and 1.51, 1.33-1.72, respectively). Women who experienced surgical menopause at earlier age (<50 years) and took HRT had lower risk of incident CHD than those who were not users of HRT. LIMITATIONS, REASONS FOR CAUTION: Self-reported data on type and age of menopause, no information on indication for the surgery (e.g. endometriosis and fibroids) and the exclusion of fatal CVD events may bias our results. WIDER IMPLICATIONS OF THE

findingsIn clinical practice, women who experienced natural menopause or had surgical menopause at an earlier age need close monitoring and engagement for preventive health measures and early diagnosis of CVD. Our findings also suggested that timing of menopause should be considered as an important factor in risk assessment of CVD for women. The findings on CVD lend some support to the position that elective bilateral oophorectomy (surgical menopause) at hysterectomy for benign diseases should be discouraged based on an increased risk of CVD. STUDY FUNDING/COMPETING INTEREST(S): InterLACE project is funded by the Australian National Health and Medical Research Council project grant (APP1027196). GDM is supported by Australian National Health and Medical Research Council Principal Research Fellowship (APP1121844). There are no competing interests.

Indexed as

Cardiovascular DiseasesMenopause, PrematureAustraliaFemaleHumansMenopauseMiddle AgedRisk AssessmentRisk Factorsage at menopausecardiovascular diseasehazard ratioHRTnatural menopausepooled analysissurgical menopause

Identifiers

PMID32563191
PMCPMC8453420
OpenAlexW3035902913

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.