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

HRT age at menopause cardiovascular disease hazard ratio natural menopause pooled analysis surgical menopause

Journal

Human reproduction (Oxford, England)
ISSN: 1460-2350
Titre abrégé: Hum Reprod
Pays: England
ID NLM: 8701199

Informations de publication

Date de publication:
01 08 2020
Historique:
received: 16 01 2020
revised: 22 04 2020
pubmed: 21 6 2020
medline: 28 4 2021
entrez: 21 6 2020
Statut: ppublish

Résumé

How does the risk of cardiovascular disease (CVD) vary with type and age of menopause? 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. 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. 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. Postmenopausal 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. 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. 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. In 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. 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.

Identifiants

pubmed: 32563191
pii: 5860261
doi: 10.1093/humrep/deaa124
pmc: PMC8453420
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1933-1943

Subventions

Organisme : Medical Research Council
ID : K013351
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RG/16/11/32334
Pays : United Kingdom
Organisme : NIA NIH HHS
ID : R01 AG017644
Pays : United States
Organisme : Medical Research Council
ID : MC UU 12019/1
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RG/13/2/30098
Pays : United Kingdom

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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Auteurs

Dongshan Zhu (D)

The University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.

Hsin-Fang Chung (HF)

The University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.

Annette J Dobson (AJ)

The University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.

Nirmala Pandeya (N)

The University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.
Department of Population Health, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Eric J Brunner (EJ)

Department of Epidemiology and Public Health, University College London, London, UK.

Diana Kuh (D)

Medical Research Council Unit for Lifelong Health and Ageing at UCL, London, UK.

Darren C Greenwood (DC)

Nutritional Epidemiology Group, School of Food Science and Nutrition, University of Leeds, Leeds, UK.

Rebecca Hardy (R)

CLOSER, UCL Institute of Education, London, UK.

Janet E Cade (JE)

Nutritional Epidemiology Group, School of Food Science and Nutrition, University of Leeds, Leeds, UK.

Graham G Giles (GG)

Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Victoria, Australia.
Centre for Epidemiology and Biostatistics, School of Population and Global Health, The University of Melbourne, Melbourne, Victoria, Australia.
Precision Medicine, School of Clinical Sciences at Monash Health, Monash University, Melbourne, Victoria, Australia.

Fiona Bruinsma (F)

Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Victoria, Australia.

Panayotes Demakakos (P)

Department of Epidemiology and Public Health, University College London, London, UK.

Mette Kildevæld Simonsen (MK)

UcDiakonissen and Parker Institute, Frederiksberg, Denmark.

Sven Sandin (S)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Elisabete Weiderpass (E)

International Agency for Research on Cancer, World Health Organisation, Lyon, France.

Gita D Mishra (GD)

The University of Queensland, Epidemiology and Biostatistics Division, School of Public Health, Brisbane, Queensland, Australia.

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