Sechi Andrea, di Altobrando Ambra, Cerciello Eugenio, Maietti Elisa, Patrizi Annalisa, Savoia Francesco
Dermatology, IRCCS Policlinico di Sant'Orsola. Department of Experimental, Diagnostic and Specialty Medicine, Alma Mater Studiorum University of Bologna, Italy.
Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy.
Dermatol Pract Concept. 2021 Apr 12;11(2):e2021031. doi: 10.5826/dpc.1102a31. eCollection 2021 Mar.
Actinic keratosis (AK) is a form of premalignant keratinocyte dysplasia. Recently, the role of photosensitizing drugs in the development of AK has been postulated.
This study evaluated a possible association between the use of photosensitizing drugs and the development of AK. A secondary aim was to identify a possible association between any medication other than those primarily examined and AK.
A single-center, case-control study assessed the cumulative drug exposure of 90 patients with AK and 90 controls visiting a dermatology service for other skin ailments. Before the visit, patients were interviewed to collect data on daily therapy and the lag-time of discontinued drugs within the last 2 years, and to record the drug's active ingredient, dosage, and duration of therapy. In addition, sociodemographic characteristics including age, sex, educational level, skin phototype, and cumulative sun exposure habits were gathered.
By logistic regression, exposures to angiotensin II receptor blockers (ARBs) and antiplatelet agents were identified as independent risk factors for the development of AK. ARB intake was associated with AK only at high exposure (OR = 13.6; 95% CI, 2.0-93.8). The use of antiplatelet drugs was borderline, yet not significant, at low exposure (OR = 3.31; 95% CI, 0.86-12.7), but increased in a dose-dependent manner. The strongest correlation was found at the highest cumulative dose (>1100 dose unit-years (OR = 4.38; 95% CI, 1.16-16.6).
High exposure to ARBs and antiplatelet agents may promote AK carcinogenesis in at-risk patients.
光化性角化病(AK)是一种癌前角质形成细胞发育异常的形式。最近,有人推测光敏药物在AK发生发展中的作用。
本研究评估了光敏药物的使用与AK发生之间的可能关联。第二个目的是确定除主要研究药物之外的任何药物与AK之间的可能关联。
一项单中心病例对照研究评估了90例AK患者和90名因其他皮肤疾病就诊于皮肤科的对照者的累积药物暴露情况。就诊前,对患者进行访谈,收集过去2年内每日治疗情况和停药滞后时间的数据,并记录药物的活性成分、剂量和治疗持续时间。此外,还收集了包括年龄、性别、教育程度、皮肤光类型和累积日晒习惯等社会人口学特征。
通过逻辑回归分析,发现使用血管紧张素II受体阻滞剂(ARB)和抗血小板药物是AK发生的独立危险因素。仅在高暴露水平时,ARB摄入与AK相关(比值比[OR]=13.6;95%置信区间[CI],2.0-93.8)。低暴露水平时,抗血小板药物的使用接近临界值,但无统计学意义(OR=3.31;95%CI,0.86-12.7),但呈剂量依赖性增加。在最高累积剂量(>1100剂量单位-年)时发现最强相关性(OR=4.38;95%CI,1.16-16.6)。
高暴露于ARB和抗血小板药物可能促进高危患者的AK癌变。