Department of Dermatology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Groningen Research Institute of Pharmacy, Unit PharmacoTherapy, -Epidemiology &-Economics, University of Groningen, Groningen, The Netherlands.
Acta Derm Venereol. 2023 Apr 4;103:adv3933. doi: 10.2340/actadv.v103.3933.
Photosensitizing properties of hydrochlorothiazide may increase skin cancer risk. To date, study findings on the association between hydrochlorothiazide use and skin cancer risk are inconsistent, notably regarding confounding and dose-response. The aim of this study was to investigate the association between hydrochlorothiazide use and incidence of skin cancer in a cohort of unselected Caucasian adults, taking dosing into account. As part of the PharmLines Initiative, which links data from the Lifelines Cohort Study and prescription database IADB.nl, patients aged ≥ 40 years were included from Lifelines, a prospective population-based cohort study in the north of the Netherlands. Skin cancer incidence was compared between subjects starting hydrochlorothiazide treatment (n = 608), subjects starting treatment with other antihypertensives (n = 508), and non-antihypertensive long-term medication users (n = 1,710). Cox regression analyses were performed to obtain hazard ratios, adjusted for potential confounders. The risk of any skin cancer, keratinocyte carcinoma, basal cell carcinoma and squamous cell carcinoma was not significantly increased in general hydrochlorothiazide users. A clear association was observed between high cumulative hydrochlorothiazide use (≥ 5,000 defined daily dose; ≥ 125,000 mg) and the risk of any skin cancer (adjusted hazard ratio 5.32, 95% confidence interval (95% CI) 2.40-11.81), keratinocyte carcinoma (adjusted hazard ratio 7.31, 95% CI 3.12-17.13), basal cell carcinoma (adjusted hazard ratio 7.72, 95% CI 3.11-19.16) and squamous cell carcinoma (adjusted hazard ratio 19.63, 95% CI 3.12-123.56). These findings should lead to awareness with high use of hydrochlorothiazide in Caucasian adults.
氢氯噻嗪的光敏特性可能会增加皮肤癌风险。迄今为止,关于氢氯噻嗪使用与皮肤癌风险之间的关联的研究结果并不一致,特别是关于混杂因素和剂量反应。本研究旨在调查在未选择的白种成年人队列中,考虑到剂量,氢氯噻嗪使用与皮肤癌发病之间的关联。作为 PharmLines 倡议的一部分,该倡议将 Lifelines 队列研究和 IADB.nl 处方数据库的数据联系起来,从荷兰北部的一项前瞻性基于人群的 Lifelines 队列研究中纳入了年龄≥40 岁的患者。将开始氢氯噻嗪治疗的患者(n=608)、开始其他降压药治疗的患者(n=508)和非降压长期用药患者(n=1710)的皮肤癌发病率进行比较。使用 Cox 回归分析获得风险比,调整了潜在混杂因素。一般氢氯噻嗪使用者的任何皮肤癌、角质形成细胞癌、基底细胞癌和鳞状细胞癌风险没有显著增加。观察到高累积氢氯噻嗪使用(≥5000 定义日剂量;≥125000mg)与任何皮肤癌(调整后的危险比 5.32,95%置信区间[95%CI]2.40-11.81)、角质形成细胞癌(调整后的危险比 7.31,95%CI 3.12-17.13)、基底细胞癌(调整后的危险比 7.72,95%CI 3.11-19.16)和鳞状细胞癌(调整后的危险比 19.63,95%CI 3.12-123.56)之间存在明确关联。这些发现应该引起人们对白种成年人中氢氯噻嗪高用量的认识。