Association of hydralazine use with risk of hematologic neoplasms in patients with hypertension: A nationwide population-based cohort study in Taiwan

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Abstract

Background Onco-hypertension recognizes well-controlled blood pressure as a favorable prognostic factor for survival in patients with hypertension and solid tumors, including hematologic neoplasms. However, it remains unknown whether continuous use of hydralazine—an antihypertensive agent (AHA) with notable anti-neoplastic activity—is associated with a lower risk of hematologic neoplasms compared to other AHAs. Method and findings Utilizing Taiwan’s National Health Insurance Research Database, we conducted a 16-year follow-up study (2000–2015) involving 375,107 patients with hypertension treated with an AHA for ≥180 days. The patients with hypertension were divided into two groups based on hydralazine prescription duration: an exposure group (hydralazine ≥180 days; n=59,786) and a reference group (hydralazine <180 days; n=239,144) after 1:4 matching for sex, age, and index date with the exposure group. Both groups were well-matched, with a mean age of approximately 60.8 years and 52.19% male. We assess the association between hydralazine use and the risk of hematologic neoplasms using Kaplan–Meier analysis and multivariable Cox proportional hazards regression, with models adjusted for concomitant medications possessing potential anti-neoplastic properties. The 16-year cumulative incidence of hematologic neoplasms was lower in the exposure group (105.58 per 100,000 person-years) than in the reference group (160.33). Accounting for death as competing risk, the exposure group exhibited an adjusted subdistribution hazard ratio (adjusted sHR) of 0.789 (95% confidence interval [0.667,0.913]; P

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Wang, L. T., Chien, W. C., Ma, K. S. K., Chung, C. H., Chen, Y. C., Tsai, W. C., & Yang, B. H. (2025). Association of hydralazine use with risk of hematologic neoplasms in patients with hypertension: A nationwide population-based cohort study in Taiwan. PLOS Medicine, 22(12). https://doi.org/10.1371/journal.pmed.1004646

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