Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, Taipei, Taiwan.
Department of Dermatology, National Taiwan University Hospital Hsin-Chu Branch, Hsinchu, Taiwan.
Drug Saf. 2018 Mar;41(3):285-295. doi: 10.1007/s40264-017-0614-2.
Several case studies have reported an association between antifungal drug use and psoriasis risk.
The objective of this study was to investigate the association between terbinafine/itraconazole exposure and psoriasis incidence.
Among patients with onychomycosis in the Taiwan National Health Insurance Research Database, 3831 incident psoriasis cases were identified during 2004-2010 and compared with 3831 age- and sex-matched controls with the same look-back period. Multivariate conditional logistic regression was used for the analysis.
The psoriasis cases were significantly more likely than matched controls to have used terbinafine or itraconazole (59.85 vs. 42.70%, respectively; p < 0.0001). After adjusting for potential confounders and cumulative duration of antifungal drug prescription, terbinafine/itraconazole use was associated with an increased psoriasis risk (adjusted odds ratio 1.33, 95% confidence interval 1.15-1.54). The association was stronger for more recent drug exposure (adjusted odds ratio 2.96, 95% confidence interval 2.25-3.90 for ≤ 90 days before the sampling date; adjusted odds ratio 1.04, 95% confidence interval 0.89-1.22 for > 360 days). In a comparison of patients receiving terbinafine or itraconazole only, psoriasis risk was higher for itraconazole (adjusted odds ratio 1.21, 95% confidence interval 1.05-1.40).
This large population-based case-control analysis showed that exposure to terbinafine or itraconazole is associated with an increased risk of incident psoriasis. The finding of an increased psoriasis risk for antifungal drug users, particularly for itraconazole, deserves attention in clinical practice although further prospective studies are necessary to confirm our findings and clarify the biological mechanisms that underlie these associations.
几项病例研究报告了抗真菌药物使用与银屑病风险之间的关联。
本研究旨在调查特比萘芬/伊曲康唑暴露与银屑病发病风险之间的关联。
在台湾全民健康保险研究数据库中,在 2004-2010 年期间,共确定了 3831 例银屑病新发病例,并与具有相同回溯期的 3831 名年龄和性别匹配的对照者进行了比较。采用多变量条件逻辑回归进行分析。
银屑病病例组患者使用特比萘芬或伊曲康唑的可能性显著高于匹配对照组(分别为 59.85%和 42.70%;p<0.0001)。在调整了潜在混杂因素和抗真菌药物处方累积持续时间后,特比萘芬/伊曲康唑的使用与银屑病发病风险增加相关(调整后的优势比 1.33,95%置信区间 1.15-1.54)。最近的药物暴露与更强的关联相关(在采样日期前≤90 天的调整后优势比为 2.96,95%置信区间为 2.25-3.90;在采样日期前>360 天的调整后优势比为 1.04,95%置信区间为 0.89-1.22)。在比较仅接受特比萘芬或伊曲康唑治疗的患者时,伊曲康唑的银屑病风险更高(调整后的优势比 1.21,95%置信区间 1.05-1.40)。
这项基于人群的大型病例对照分析表明,特比萘芬或伊曲康唑的暴露与新发银屑病的风险增加相关。抗真菌药物使用者银屑病风险增加的发现,特别是伊曲康唑,值得在临床实践中关注,尽管需要进一步的前瞻性研究来证实我们的发现并阐明这些关联背后的生物学机制。