Histamine H 2 Receptor Antagonists and Heart Failure Risk in Postmenopausal Women: The Women’s Health Initiative

Author:

Larson Sophia R.1ORCID,Vasbinder Alexi L.2,Reding Kerryn W.3,Leary Peter J.4ORCID,Branch Kelley R.1ORCID,Shadyab Aladdin H.5,Johnson Karen C.6,Haring Bernhard7ORCID,Wallace Robert8,Manson JoAnn E.9ORCID,Anderson Garnet10,Cheng Richard K.1ORCID

Affiliation:

1. Division of Cardiology Department of Medicine University of Washington Seattle WA

2. Department of Health Informatics School of Nursing University of Washington Seattle WA

3. Department of Biobehavioral Nursing and Health Informatics School of Nursing University of Washington Seattle WA

4. Division of Pulmonology and Critical Care Medicine Department of Medicine University of Washington Seattle WA

5. Herbert Wertheim School of Public Health and Human Longevity Science University of California, San Diego La Jolla CA

6. Department of Preventive Medicine University of Tennessee Health Science Center Memphis TN

7. Department of Internal Medicine Saarland University Homburg Germany

8. Departments of Epidemiology and Medicine University of Iowa Iowa City IA

9. Department of Medicine Brigham and Women's Hospital Harvard Medical School Boston MA

10. Public Health Sciences Division Fred Hutchinson Cancer Research Center Seattle WA

Abstract

Background Prior studies suggested lower risk of heart failure (HF) in individuals taking H 2 receptor antagonists (H2RA) compared with H2RA nonusers in relatively small studies. We evaluated the association of H2RA use and incident HF in postmenopausal women in the large‐scale WHI (Women’s Health Initiative) study. Methods and Results This study included postmenopausal women from the WHI without a history of HF at baseline. HF was defined as first incident hospitalization for HF and physician adjudicated. Multivariable Cox proportional hazards regression models evaluated the association of H2RA use as a time‐varying exposure with HF risk, after adjustment for demographic, lifestyle, and medical history variables. Sensitivity analyses examined (1) risk of HF stratified by the ARIC (Atherosclerosis Risk in Communities) score, (2) propensity score matching on H2RA use, (3) use of proton pump inhibitors rather than H2RA nonuse as the referent, and (4) exclusion of those taking diuretics at baseline. The primary analysis included 158 854 women after exclusion criteria, of whom 9757 (6.1%) were H2RA users. During median 8.2 years of follow‐up, 376 H2RA users (4.9 events/1000 person‐years) and 3206 nonusers (2.7 events/1000 person‐years) developed incident HF. After multivariable adjustment, there was no association between H2RA use and HF in the primary analysis (hazard ratio, 1.07; 95% CI, 0.94–1.22; P =0.31) or in any of the sensitivity analyses. Conclusions Clinical H2RA use was not associated with incident HF among postmenopausal women. Future studies are needed to evaluate potential effect modification by sex, HF severity, or patterns of use on H2RA exposure and HF risk. Registration URL: https://www.clinicaltrials.gov ; Unique identifier: NCT00000611.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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