TY - JOUR
T1 - Menopausal hormone therapy and mortality
T2 - A systematic review and meta-analysis
AU - Benkhadra, Khalid
AU - Mohammed, Khaled
AU - Al Nofal, Alaa
AU - Carranza Leon, Barbara G.
AU - Alahdab, Fares
AU - Faubion, Stephanie
AU - Montori, Victor M.
AU - Dabrh, Abd Moain Abu
AU - Hernández, Jorge Alberto Zúñiga
AU - Prokop, Larry J.
AU - Murad, Mohammad Hassan
N1 - Publisher Copyright:
Copyright © 2015 by the Endocrine Society.
PY - 2015/11
Y1 - 2015/11
N2 - Objectives: The objective was to assess the effect of menopausal hormonal therapy (MHT) on all-cause and cause-specific mortality. Methods: We conducted a comprehensive search of several databases (MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials and Database of Systematic Reviews, and Scopus) from inception until August 2013. We included randomized controlled trials (RCTs) of more than 6 months of duration comparing MHT with no treatment. Pairs of independent reviewers selected trials, assessed risk of bias and extracted data. We estimated risk ratios (RRs) and 95% confidence intervals (CIs) using the random-effects model. Results:Weincluded 43 RCTs at moderate risk of bias. Meta-analysis showed no effect on mortality (RR 0.99[95%CI, 0.94-1.05]), regardless ofMHTtype or history of preexisting heart disease.Noassociation was found between MHT and cardiac death (RR 1.04 [95% CI 0.87-1.23]) or stroke (RR 1.49 [95% CI 0.95-2.31]). Estrogen plus progesterone use was associated with a likely increase in breast cancer mortality (RR 1.96[95%CI 0.98-3.94]),whereasestrogen usewasnot.MHTusewasnot associated with mortality of other types of cancer. In 5 trials,MHTwaslikely started at a younger age: 2 RCTs withmean agelessthan60and3RCTswithMHTstarted lessthan10years aftermenopause.Meta-analysis of these 5 RCTs showed a reduction of mortality with MHT (RR 0.70 [95% CI 0.52-0.95]). Conclusion: The current evidence suggests that MHT does not affect the risk of death from all causes, cardiac death and death from stroke or cancer. These data may be used to support clinical and policy deliberations about the role of MHT in the care of symptomatic postmenopausal women.
AB - Objectives: The objective was to assess the effect of menopausal hormonal therapy (MHT) on all-cause and cause-specific mortality. Methods: We conducted a comprehensive search of several databases (MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials and Database of Systematic Reviews, and Scopus) from inception until August 2013. We included randomized controlled trials (RCTs) of more than 6 months of duration comparing MHT with no treatment. Pairs of independent reviewers selected trials, assessed risk of bias and extracted data. We estimated risk ratios (RRs) and 95% confidence intervals (CIs) using the random-effects model. Results:Weincluded 43 RCTs at moderate risk of bias. Meta-analysis showed no effect on mortality (RR 0.99[95%CI, 0.94-1.05]), regardless ofMHTtype or history of preexisting heart disease.Noassociation was found between MHT and cardiac death (RR 1.04 [95% CI 0.87-1.23]) or stroke (RR 1.49 [95% CI 0.95-2.31]). Estrogen plus progesterone use was associated with a likely increase in breast cancer mortality (RR 1.96[95%CI 0.98-3.94]),whereasestrogen usewasnot.MHTusewasnot associated with mortality of other types of cancer. In 5 trials,MHTwaslikely started at a younger age: 2 RCTs withmean agelessthan60and3RCTswithMHTstarted lessthan10years aftermenopause.Meta-analysis of these 5 RCTs showed a reduction of mortality with MHT (RR 0.70 [95% CI 0.52-0.95]). Conclusion: The current evidence suggests that MHT does not affect the risk of death from all causes, cardiac death and death from stroke or cancer. These data may be used to support clinical and policy deliberations about the role of MHT in the care of symptomatic postmenopausal women.
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U2 - 10.1210/jc.2015-2238
DO - 10.1210/jc.2015-2238
M3 - Review article
C2 - 26544652
AN - SCOPUS:84958632292
SN - 0021-972X
VL - 100
SP - 4021
EP - 4028
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 11
ER -