Associations of Oral Contraceptive Use With Cardiovascular Disease and All‐Cause Death: Evidence From the UK Biobank Cohort Study

Author:

Dou Weijuan1234ORCID,Huang Yan1345,Liu Xuesong6,Huang Chensihan1,Huang Junlin1,Xu Bingyan1ORCID,Yang Linjie1,Liu Yating1,Lei Xuzhen1ORCID,Li Xu1,Huang Junfeng1ORCID,Lin Jiayang1ORCID,Liu Deying1,Zhang Peizhen1,Shao Jiaqing2,Liu Changqin7,Zhang Huijie1345ORCID

Affiliation:

1. Department of Endocrinology and Metabolism, Nanfang Hospital Southern Medical University Guangzhou China

2. Department of Endocrinology, Jinling Hospital Medical School of Nanjing University Nanjing China

3. Guangdong Provincial Key Laboratory of Cardiac Function and Microcirculation Guangzhou China

4. State Key Laboratory of Organ Failure Research, National Clinical Research Center for Kidney Disease Nanfang Hospital, Southern Medical University Guangzhou China

5. Department of Food Safety and Health Research Center, School of Public Health Southern Medical University Guangzhou Guangdong China

6. State Key Lab of Respiratory Diseases, Guangzhou Institute of Respiratory Health, Department of Critical Care Medicine The First Affiliated Hospital of Guangzhou Medical University Guangzhou China

7. Department of Endocrinology and Metabolism The First Affiliated Hospital of Xiamen University Xiamen China

Abstract

Background The associations of oral contraceptive (OC) use with cardiovascular disease (CVD) and all‐cause death remains unclear. We aimed to determine the associations of OC use with incident CVD and all‐cause death. Methods and Results This cohort study included 161 017 women who had no CVD at baseline and reported their OC use. We divided OC use into ever use and never use. Cox proportional hazard models were used to calculate hazard ratios and 95% CIs for cardiovascular outcomes and death. Overall, 131 131 (81.4%) of 161 017 participants reported OC use at baseline. The multivariable‐adjusted hazard ratios for OC ever users versus never users were 0.92 (95% CI, 0.86–0.99) for all‐cause death, 0.91 (95% CI, 0.87–0.96) for incident CVD events, 0.88 (95% CI, 0.81–0.95) for coronary heart disease, 0.87 (95% CI, 0.76–0.99) for heart failure, and 0.92 (95% CI, 0.84–0.99) for atrial fibrillation. However, no significant associations of OC use with CVD death, myocardial infarction, or stroke were observed. Furthermore, the associations of OC use with CVD events were stronger among participants with longer durations of use ( P for trend<0.001). Conclusions OC use was not associated with an increased risk of CVD events and all‐cause death in women and may even produce an apparent net benefit. In addition, the beneficial effects appeared to be more apparent in participants with longer durations of use.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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