Association of alpha-1-adrenergic antagonist use with the risk of gout development in benign prostatic hyperplasia patients: a population-based cohort study

Author:

Hsu Wei-Hung1ORCID,Lai Jung-Nien23ORCID,Lin Cheng-Li24ORCID,Loh Ching-Hui56ORCID,Huang Huei-Kai17ORCID,Huang Liang-Kai18ORCID

Affiliation:

1. Department of Family Medicine, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan

2. School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan

3. Department of Chinese Medicine, China Medical University Hospital, Taichung, Taiwan

4. Management Office for Health Data (DryLab), Clinical Trial Center (CTC), China Medical University Hospital, Taichung, Taiwan

5. School of Medicine, Tzu Chi University, Hualien, Taiwan

6. Center for Aging and Health, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan

7. Department of Medical Research, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan

8. Center for Preventive Medicine, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan

Abstract

Abstract Background Men are more likely to develop benign prostatic hyperplasia (BPH) and gout as they age. However, the role of alpha-1-adrenergic antagonists, the medication for BPH, in the development of gout is uncertain. Objective To investigate the effect of alpha-1-adrenergic antagonist use on the risk of developing gout in BPH patients. Methods Data of patients with newly diagnosed BPH were retrieved from Taiwan’s 2000–2013 National Health Insurance Research Database (total number: 15,390 patients; 7,695 patients in each cohort). Propensity score matching was conducted according to age, comorbidities, medication history for cohorts that received or did not receive alpha-1-adrenergic antagonists. Hazard ratios (HRs) were assessed for gout development using Cox proportional hazards regression models. Results Use of alpha-1-adrenergic antagonists was not associated with gout development in BPH patients (HR = 0.92; 95% confidence interval [CI], 0.78–1.10; P = 0.35). However, after stratification according to the average number of days of alpha-1-adrenergic antagonist use per year, patients with an average of >300 days had a significantly higher risk of gout development than patients who did not receive alpha-1-adrenergic antagonists (adjusted HR = 1.57; 95% CI, 1.25–1.97; P < 0.001). Patients with more days of medication use per year had a higher risk of gout development than those with fewer days of medication use (P < 0.001). Conclusion Patients who received more doses of alpha-1-adrenergic antagonists per year had a higher risk of developing gout. A causal proof of the role of alpha-1-adrenergic antagonists use in gout development should be analysed in future studies designed as double blind randomized controlled trials.

Funder

Taiwan Ministry of Health

Welfare Clinical Trial Center

MOST Clinical Trial Consortium for Stroke

Publisher

Oxford University Press (OUP)

Subject

Family Practice

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