Sex-Specific Effects of Blood Pressure Lowering Pharmacotherapy for the Prevention of Cardiovascular Disease: An Individual Participant-Level Data Meta-Analysis

Author:

Bidel Zeinab123ORCID,Nazarzadeh Milad12ORCID,Canoy Dexter123ORCID,Copland Emma123ORCID,Gerdts Eva4ORCID,Woodward Mark56ORCID,Gupta Ajay K.7ORCID,Reid Christopher M.8ORCID,Cushman William C.9ORCID,Wachtell Kristian10ORCID,Teo Koon11,Davis Barry R.12ORCID,Chalmers John6ORCID,Pepine Carl J.13ORCID,Rahimi Kazem123ORCID,

Affiliation:

1. Deep Medicine, Oxford Martin School (Z.B., M.N., D.C., E.C., K.R.), University of Oxford, United Kingdom.

2. Nuffield Department of Women’s and Reproductive Health (Z.B., M.N., D.C., E.C., K.R.), University of Oxford, United Kingdom.

3. NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, United Kingdom (Z.B., D.C., E.C., K.R.).

4. Department of Clinical Science, Centre for Research on Cardiac Disease in Women, University of Bergen, Norway (E.G.).

5. The George Institute for Global Health, School of Public Health, Imperial College London, United Kingdom (M.W.).

6. The George Institute for Global Health, University of New South Wales, Sydney, Australia (M.W., J.C.).

7. William Harvey Research Institute, Queen Mary University of London, United Kingdom (A.K.G.).

8. School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia (C.M.R.).

9. Department of Preventive Medicine, The University of Tennessee Health Science Center, Memphis (W.C.C.).

10. Department of Cardiology, NewYork-Presbyterian/Weill Cornell Medical Center (K.W.).

11. Population Health Research Institute, Hamilton Health Sciences, McMaster University, Ontario, Canada (K.T.).

12. The University of Texas School of Public Health, Houston (B.R.D.).

13. College of Medicine, University of Florida, Gainesville (C.J.P.).

Abstract

BACKGROUND: Whether the relative effects of blood pressure (BP)–lowering treatment on cardiovascular outcomes differ by sex, particularly when BP is not substantially elevated, has been uncertain. METHODS: We conducted an individual participant-level data meta-analysis of randomized controlled trials of pharmacological BP lowering. We pooled the data and categorized participants by sex, systolic BP categories in 10-mm Hg increments from <120 to ≥170 mm Hg, and age categories spanning from <55 to ≥85 years. We used fixed-effect one-stage individual participant-level data meta-analyses and applied Cox proportional hazard models, stratified by trial, to analyze the data. RESULTS: We included data from 51 randomized controlled trials involving 358 636 (42% women) participants. Over 4.2 years of median follow-up, a 5-mm Hg reduction in systolic BP decreased the risk of major cardiovascular events both in women and men (hazard ratio [95% CI], 0.92 [0.89–0.95] for women and 0.90 [0.88–0.93] for men; P for interaction, 1). There was no evidence for heterogeneity of relative treatment effects by sex for the major cardiovascular disease, its components, or across the different baseline BP categories (all P for interaction, ≥0.57). The effects in women and men were consistent across age categories and the types of antihypertensive medications (all P for interaction, ≥0.14). CONCLUSIONS: The effects of BP reduction were similar in women and men across all BP and age categories at randomization and with no evidence to suggest that drug classes had differing effects by sex. This study does not substantiate sex-based differences in BP-lowering treatment.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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