Photosensitizing antihypertensive medication and risk of skin cancer among postmenopausal women.

Jiali Han, Eunyoung Cho, Abrar Qureshi, Yueyao Li, Charles B Eaton, Aladdin H Shadyab, Alexander Hou

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2024;22(2):186-194

PMID: 38345266

Abstract

BACKGROUND

Few prospective studies exist with an evaluation of a dose-response relationship between use of some photosensitizing antihypertensive medications and skin cancer.

PATIENT AND METHODS

We used prospective data from the Women's Health Initiative Observational Study to investigate the association between antihypertensive use and risk of non-melanoma skin cancer (NMSC) and melanoma in postmenopausal women aged 50-79 years at baseline (n  =  64,918). Multivariable Cox proportional hazards regression models were used and hazard ratios (HRs) and 95 confidence intervals (CIs) were calculated.

RESULTS

8,777 NMSC and 1,227 melanoma cases were observed. Use of antihypertensives (HR [95% CI]: 1.12 [1.07-1.18]), ACE inhibitors (1.09 [1.01-1.18]), calcium channel blockers (1.13 [1.05-1.22]), diuretics (1.20 [1.12-1.27]), loop diuretics (1.17 [1.07-1.28]), and thiazides (1.17 [1.03-1.33]) were each associated with higher NMSC risk. NMSC risk linearly increased with use of multiple antihypertensives (p-trend  =  0.02) and with longer duration of use (p-trend < 0.01). Antihypertensives (1.15 [1.00-1.31]), angiotensin-II receptor blockers (1.82 [1.05-3.15]), and diuretics (1.34 [1.13-1.59]) were each associated with elevated melanoma risk. Effect modification by solar radiation exposure was found between antihypertensive use and incidence of melanoma (p-interaction  =  0.02).

CONCLUSIONS

Use of antihypertensives overall, and several individual classes thereof, were associated with higher incidence of NMSC and melanoma with dose-response relationship.

© 2024 Deutsche Dermatologische Gesellschaft (DDG).

Address: Department of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, USA.; Department of Dermatology, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.; Herbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego, CA, La Jolla, USA.; Department of Epidemiology, Indiana University Richard M. Fairbanks School of Public Health, Indianapolis, Indiana, USA.; Department of Family Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.; Department of Epidemiology, School of Public Health, Brown University, Providence, Rhode Island, USA.; Department of Dermatology, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.; Department of Epidemiology, School of Public Health, Brown University, Providence, Rhode Island, USA.; Department of Dermatology, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.; Department of Epidemiology, School of Public Health, Brown University, Providence, Rhode Island, USA.; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, MA, Boston, USA.
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