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      Menopausal hormone therapy and women’s health: An umbrella review

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          Abstract

          Background

          There remains uncertainty about the impact of menopausal hormone therapy (MHT) on women’s health. A systematic, comprehensive assessment of the effects on multiple outcomes is lacking. We conducted an umbrella review to comprehensively summarize evidence on the benefits and harms of MHT across diverse health outcomes.

          Methods and findings

          We searched MEDLINE, EMBASE, and 10 other databases from inception to November 26, 2017, updated on December 17, 2020, to identify systematic reviews or meta-analyses of randomized controlled trials (RCTs) and observational studies investigating effects of MHT, including estrogen-alone therapy (ET) and estrogen plus progestin therapy (EPT), in perimenopausal or postmenopausal women in all countries and settings. All health outcomes in previous systematic reviews were included, including menopausal symptoms, surrogate endpoints, biomarkers, various morbidity outcomes, and mortality. Two investigators independently extracted data and assessed methodological quality of systematic reviews using the updated 16-item AMSTAR 2 instrument. Random-effects robust variance estimation was used to combine effect estimates, and 95% prediction intervals (PIs) were calculated whenever possible. We used the term MHT to encompass ET and EPT, and results are presented for MHT for each outcome, unless otherwise indicated. Sixty systematic reviews were included, involving 102 meta-analyses of RCTs and 38 of observational studies, with 102 unique outcomes. The overall quality of included systematic reviews was moderate to poor. In meta-analyses of RCTs, MHT was beneficial for vasomotor symptoms (frequency: 9 trials, 1,104 women, risk ratio [RR] 0.43, 95% CI 0.33 to 0.57, p < 0.001; severity: 7 trials, 503 women, RR 0.29, 95% CI 0.17 to 0.50, p = 0.002) and all fracture (30 trials, 43,188 women, RR 0.72, 95% CI 0.62 to 0.84, p = 0.002, 95% PI 0.58 to 0.87), as well as vaginal atrophy (intravaginal ET), sexual function, vertebral and nonvertebral fracture, diabetes mellitus, cardiovascular mortality (ET), and colorectal cancer (EPT), but harmful for stroke (17 trials, 37,272 women, RR 1.17, 95% CI 1.05 to 1.29, p = 0.027) and venous thromboembolism (23 trials, 42,292 women, RR 1.60, 95% CI 0.99 to 2.58, p = 0.052, 95% PI 1.03 to 2.99), as well as cardiovascular disease incidence and recurrence, cerebrovascular disease, nonfatal stroke, deep vein thrombosis, gallbladder disease requiring surgery, and lung cancer mortality (EPT). In meta-analyses of observational studies, MHT was associated with decreased risks of cataract, glioma, and esophageal, gastric, and colorectal cancer, but increased risks of pulmonary embolism, cholelithiasis, asthma, meningioma, and thyroid, breast, and ovarian cancer. ET and EPT had opposite effects for endometrial cancer, endometrial hyperplasia, and Alzheimer disease. The major limitations include the inability to address the varying effects of MHT by type, dose, formulation, duration of use, route of administration, and age of initiation and to take into account the quality of individual studies included in the systematic reviews. The study protocol is publicly available on PROSPERO (CRD42017083412).

          Conclusions

          MHT has a complex balance of benefits and harms on multiple health outcomes. Some effects differ qualitatively between ET and EPT. The quality of available evidence is only moderate to poor.

          Abstract

          In an umbrella review, Guo-Qiang Zhang and colleagues comprehensively summarize evidence on the benefits and harms of menopausal hormone therapy across diverse health outcomes.

          Author summary

          Why was this study done?
          • By 2050, it is estimated that worldwide more than 1.6 billion women will have reached menopause or be postmenopausal, up from 1 billion in 2020.

          • Up to 75% of menopausal women are affected by bothersome menopausal symptoms, such as hot flashes and night sweats.

          • Menopausal hormone therapy (MHT) is the most effective treatment for alleviating menopausal symptoms, but its effects on numerous health outcomes remain uncertain.

          What did the researchers do and find?
          • We included 60 published systematic reviews of MHT use in menopausal women, involving 102 meta-analyses of randomized controlled trials and 38 of observational studies, and synthesized the evidence on 102 health outcomes.

          • Overall, MHT had a complex balance of benefits and harms; for example, beyond alleviation of menopausal symptoms, it was associated with decreased risks of bone fracture, diabetes mellitus, and esophageal, gastric, and colorectal cancer, but increased risks of stroke, venous thromboembolism, gallbladder disease, and breast and ovarian cancer.

          • The available clinical data in support of MHT reducing the risk of coronary heart disease and all-cause mortality in women aged <60 years or within 10 years from menopause (known as the “timing hypothesis”) were only suggestive.

          • The overall quality of included systematic reviews was moderate to poor.

          What do these findings mean?
          • This overview of the evidence landscape could help guideline developers and decision-makers better appreciate the trade-offs between the benefits and harms associated with MHT use in menopausal women.

          • More data are needed to evaluate the timing hypothesis for coronary heart disease and all-cause mortality.

          • Clinicians should evaluate the scientific strength of systematic reviews prior to considering applying their results in clinical practice.

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          Most cited references142

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          Bias in meta-analysis detected by a simple, graphical test

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            Quantifying heterogeneity in a meta-analysis.

            The extent of heterogeneity in a meta-analysis partly determines the difficulty in drawing overall conclusions. This extent may be measured by estimating a between-study variance, but interpretation is then specific to a particular treatment effect metric. A test for the existence of heterogeneity exists, but depends on the number of studies in the meta-analysis. We develop measures of the impact of heterogeneity on a meta-analysis, from mathematical criteria, that are independent of the number of studies and the treatment effect metric. We derive and propose three suitable statistics: H is the square root of the chi2 heterogeneity statistic divided by its degrees of freedom; R is the ratio of the standard error of the underlying mean from a random effects meta-analysis to the standard error of a fixed effect meta-analytic estimate, and I2 is a transformation of (H) that describes the proportion of total variation in study estimates that is due to heterogeneity. We discuss interpretation, interval estimates and other properties of these measures and examine them in five example data sets showing different amounts of heterogeneity. We conclude that H and I2, which can usually be calculated for published meta-analyses, are particularly useful summaries of the impact of heterogeneity. One or both should be presented in published meta-analyses in preference to the test for heterogeneity. Copyright 2002 John Wiley & Sons, Ltd.
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              AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both

              The number of published systematic reviews of studies of healthcare interventions has increased rapidly and these are used extensively for clinical and policy decisions. Systematic reviews are subject to a range of biases and increasingly include non-randomised studies of interventions. It is important that users can distinguish high quality reviews. Many instruments have been designed to evaluate different aspects of reviews, but there are few comprehensive critical appraisal instruments. AMSTAR was developed to evaluate systematic reviews of randomised trials. In this paper, we report on the updating of AMSTAR and its adaptation to enable more detailed assessment of systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both. With moves to base more decisions on real world observational evidence we believe that AMSTAR 2 will assist decision makers in the identification of high quality systematic reviews, including those based on non-randomised studies of healthcare interventions.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: InvestigationRole: MethodologyRole: Project administrationRole: SoftwareRole: ValidationRole: VisualizationRole: Writing – original draftRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: InvestigationRole: ValidationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: InvestigationRole: ValidationRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: MethodologyRole: SoftwareRole: ValidationRole: VisualizationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: InvestigationRole: ValidationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: InvestigationRole: ValidationRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: Formal analysisRole: Funding acquisitionRole: InvestigationRole: SupervisionRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: SupervisionRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: SupervisionRole: VisualizationRole: Writing – review & editing
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: Project administrationRole: ResourcesRole: SupervisionRole: ValidationRole: VisualizationRole: Writing – original draftRole: Writing – review & editing
                Role: Academic Editor
                Journal
                PLoS Med
                PLoS Med
                plos
                PLoS Medicine
                Public Library of Science (San Francisco, CA USA )
                1549-1277
                1549-1676
                2 August 2021
                August 2021
                : 18
                : 8
                : e1003731
                Affiliations
                [1 ] Krefting Research Centre, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
                [2 ] Department of Geriatrics, First Affiliated Hospital of Chongqing Medical University, Chongqing, China
                [3 ] Department of Gastroenterology, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing, China
                [4 ] Quantitative Sciences Unit, Stanford University, Palo Alto, California, United States of America
                [5 ] Unit of Reproductive Endocrinology, 1st Department of Obstetrics and Gynecology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece
                [6 ] Division of Population Medicine, School of Medicine, Cardiff University, Cardiff, United Kingdom
                [7 ] UMR1086 INSERM–Unité de Recherche Interdisciplinaire pour la Prévention et le Traitement des Cancers (ANTICIPE), Centre de Lutte Contre le Cancer François Baclesse, Caen, France
                [8 ] Department of Intensive Care Unit, Chongqing General Hospital, University of Chinese Academy of Sciences, Chongqing, China
                [9 ] MRC and Asthma UK Centre in Allergic Mechanisms of Asthma, King’s College London, Guy’s Hospital, London, United Kingdom
                [10 ] Section of Reproductive and Maternal Medicine, Glasgow Royal Infirmary, School of Medicine, University of Glasgow, Glasgow, United Kingdom
                [11 ] MRC Centre for Reproductive Health, Queen’s Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom
                [12 ] Asthma UK Centre for Applied Research, Centre for Medical Informatics, Usher Institute, University of Edinburgh, Edinburgh, United Kingdom
                [13 ] Department of Respiratory Medicine, Seinäjoki Central Hospital, Seinäjoki, Finland
                [14 ] Faculty of Medicine and Health Technology, University of Tampere, Tampere, Finland
                [15 ] School of Nursing, Midwifery and Paramedic Practice, Robert Gordon University, Aberdeen, United Kingdom
                [16 ] Wallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, Gothenburg, Sweden
                University of Manchester, UNITED KINGDOM
                Author notes

                I have read the journal’s policy and the authors of this manuscript have the following competing interests: HC reports no conflicts specifically related to menopausal hormone therapy, and in the more general area of women’s health the following are declared: Grant/Research Support in AUB treatment: Bayer AG; TAP Pharmaceuticals, Preglem/Gedeon-Richter: PEARL IV (with no personal remuneration); Speaker bureau on AUB Treatment: Bayer AG, Preglem/Gedeon-Richter, Myovant (with no personal remuneration); Consultancy/Advisory Board on AUB Treatment: Bayer AG, Preglem/Gedeon-Richter, Vifor Pharma, Myovant (with no personal remuneration); Royalties from UpToDate: for an article on abnormal uterine bleeding (personal remuneration received). AS is an Academic Editor on PLOS Medicine’s editorial board. CL has co-developed extracellular vesicle-associated patents for putative clinical utilization and owns equity in Exocure Bioscience Inc. HK reports personal fees and non-financial support from AstraZeneca, personal fees from Chiesi Pharma AB, personal fees and non-financial support from Boehringer-Ingelheim, personal fees from Novartis, personal fees from Mundipharma, personal fees and non-financial support from Orion Pharma, personal fees from SanofiGenzyme, personal fees from GlaxoSmithKline, outside the submitted work. All other authors have declared that no competing interests exist.

                Author information
                https://orcid.org/0000-0002-8785-8717
                https://orcid.org/0000-0001-6698-2607
                https://orcid.org/0000-0002-8949-4312
                https://orcid.org/0000-0002-6548-358X
                https://orcid.org/0000-0002-2337-7463
                https://orcid.org/0000-0003-2998-9185
                https://orcid.org/0000-0001-7022-3056
                https://orcid.org/0000-0003-1279-1746
                https://orcid.org/0000-0001-5258-0906
                https://orcid.org/0000-0002-5997-004X
                https://orcid.org/0000-0002-2876-6089
                Article
                PMEDICINE-D-21-00766
                10.1371/journal.pmed.1003731
                8366967
                34339416
                17f61220-5b88-4384-ba66-dd75467ce35c
                © 2021 Zhang et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 14 February 2021
                : 12 July 2021
                Page count
                Figures: 4, Tables: 2, Pages: 27
                Funding
                Funded by: VBG Group Herman Krefting Foundation on Asthma and Allergy
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100005761, Sahlgrenska Akademin;
                Award Recipient :
                Funded by: Franklin E. Fetzer Memorial Trust
                Award ID: R2020-16
                Award Recipient :
                Funded by: VBG Group Herman Krefting Foundation on Asthma and Allergy
                Award Recipient :
                Funded by: Knut and Alice Wallenberg Foundation
                Award Recipient :
                Funded by: Wallenberg Centre for Molecular and Translational Medicine
                Award Recipient :
                GQZ was supported by the VBG Group Herman Krefting Foundation on Asthma and Allergy, and Sahlgrenska Academy, University of Gothenburg, Sweden. MBM was supported in part by the Franklin E. Fetzer Memorial Trust (award R2020-16). BIN was supported by the VBG Group Herman Krefting Foundation on Asthma and Allergy, Knut and Alice Wallenberg Foundation, and the Wallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, Sweden. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
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                2021-08-16
                The statistical analysis protocol and R scripts are respectively available in S3 Text and S4 and S5 Texts. The datasets are publicly available at the Open Science Framework ( https://osf.io/dsy37/; DOI: 10.17605/OSF.IO/DSY37).

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