抗高血压药物与黑色素瘤和角质细胞癌的风险:系统回顾和荟萃分析

Olivia G. Cohen , Matthew Taylor , Cassandra Mohr , Kevin T. Nead , Candice L. Hinkston , Sharon H. Giordano , Sinead M. Langan , David J. Margolis , Mackenzie R. Wehner
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引用次数: 0

摘要

有些降压药具有光敏性。由于之前的研究结果不一致,而且随着新证据的公布,对皮肤癌风险的影响仍不明确。我们进行了一项系统回顾和荟萃分析,以评估降压药与常见皮肤癌(皮肤鳞状细胞癌、基底细胞癌和黑色素瘤)之间的关系,并评估剂量反应关系。有 44 篇文章符合纳入标准,其中 42 篇可进行元分析。使用钙通道阻滞剂(相对风险 [RR] = 1.17,95% 置信区间 [CI] = 1.11-1.22)、利尿剂(RR = 1.06,95% CI = 1.03-1.10)和噻嗪类药物(RR = 1.10,95% CI = 1.04-1.16)会增加基底细胞癌的风险;使用钙通道阻滞剂会增加鳞状细胞癌的风险(RR = 1.08,95% CI = 1.01-1.14)、利尿剂(RR = 1.29,95% CI = 1.17-1.43)和噻嗪类药物(RR = 1.36,95% CI = 1.15-1.61);使用血管紧张素转换酶抑制剂治疗黑色素瘤(RR = 1.09,95% CI = 1.03-1.14)、钙通道阻滞剂(RR = 1.08,95% CI = 1.03-1.12)和噻嗪类药物(RR = 1.09,95% CI = 1.02-1.17)。证据质量较低或很低。我们观察到噻嗪类药物与基底细胞癌;血管紧张素转换酶抑制剂、利尿剂和噻嗪类药物与鳞状细胞癌;血管紧张素转换酶抑制剂、利尿剂和噻嗪类药物与黑色素瘤的剂量反应证据。我们的荟萃分析支持某些降压药(尤其是利尿剂)与皮肤癌风险之间可能存在因果关系。
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Antihypertensive Medications and Risk of Melanoma and Keratinocyte Carcinomas: A Systematic Review and Meta-Analysis

Some antihypertensive medications are photosensitizing. The implications for skin cancer risk remain unclear because results from prior studies are inconsistent and as new evidence is published. We performed a systematic review and meta-analysis to evaluate the association between antihypertensives and common skin cancers (cutaneous squamous cell carcinoma, basal cell carcinoma, and melanoma) and to evaluate dose–response relationships. Forty-four articles met inclusion criteria, and 42 could be meta analyzed. Increased risks were seen for basal cell carcinoma with calcium channel blockers (relative risk [RR] = 1.17, 95% confidence interval [CI] = 1.11–1.22), diuretics (RR = 1.06, 95% CI = 1.03–1.10), and thiazides (RR = 1.10, 95% CI = 1.04–1.16); for squamous cell carcinoma with calcium channel blockers (RR = 1.08, 95% CI = 1.01–1.14), diuretics (RR = 1.29, 95% CI = 1.17–1.43), and thiazides (RR = 1.36, 95% CI = 1.15–1.61); and for melanoma in angiotensin-converting enzyme inhibitors (RR = 1.09, 95% CI = 1.03–1.14), calcium channel blockers (RR = 1.08, 95% CI = 1.03–1.12), and thiazides (RR = 1.09, 95% CI = 1.02–1.17). The quality of evidence was low or very low. We observed evidence for dose–response for thiazides with basal cell carcinoma; angiotensin-converting enzyme inhibitors, diuretics, and thiazides with squamous cell carcinoma; and angiotensin-converting enzyme inhibitors, diuretics, and thiazides with melanoma. Our meta-analysis supports a potential causal association between some antihypertensives, particularly diuretics, and skin cancer risk.

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CiteScore
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8 weeks
期刊最新文献
Cover 1 Corrigendum to ‘Proteomic Profiling of CCCA Reveals Role of Humoral Immune Response Pathway and Metabolic Dysregulation’ JID Innovations, Volume 4, Issue 3, May 2024, 100263 Identification of Associations with Dermatologic Diseases through a Focused GWAS of the UK Biobank From Plant to Patient: A Historical Perspective and Review of Selected Medicinal Plants in Dermatology Spatial Transcriptomics in Inflammatory Skin Diseases Using GeoMx Digital Spatial Profiling: A Practical Guide for Applications in Dermatology
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