Department of Internal Medicine, Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Republic of Korea.
Dermatology. 2021;237(3):330-337. doi: 10.1159/000514030. Epub 2021 Feb 8.
Emerging data suggest that inflammatory bowel disease (IBD) and psoriasis are associated, sharing common genetic predispositions and immunological mechanisms. However, concrete data on psoriasis risk in IBD patients compared to the general population are limited.
We investigated the risk of developing psoriasis in IBD patients compared to controls without IBD.
Using the Korean National Health Insurance Database, patients diagnosed with Crohn's disease (CD) or ulcerative colitis (UC) between 2005 and 2008 were age- and sex-matched 1:4 to non-IBD subjects from 2003 to 2018. IBD patients were defined by combining the International Classification of Diseases 10th revision code and at least one prescription of IBD-specific medications. Disease phenotypes, including psoriasis severity and psoriatic arthritis, were also identified. We investigated newly diagnosed psoriasis from 2009 to 2018. Incidence rates and risk of psoriasis were assessed with multivariate Cox regression models. Subgroup analyses for age and sex, and sensitivity analysis involving tumor necrosis factor (TNF) inhibitor-naïve patients were performed.
During nearly a decade of follow-up, 20,152 IBD patients were identified (14,619 [72.54%] UC and 5,533 [27.46%] CD). Among them, 439 patients were newly diagnosed with psoriasis (incidence rate of 217.68 per 100,000 person-years and 228.62 per 100,000 person-years for UC and CD, respectively). The psoriasis risk was higher in IBD patients than in the matched controls (adjusted hazard ratio, aHR, 2.95, 95% confidence interval, CI, 2.60-3.33). Moreover, IBD patients aged <30 years were at an increased risk (aHR 3.35, 95% CI 2.58-4.35), a trend that was unchanged across all psoriasis phenotypes. Sensitivity analysis of TNF inhibitor-naïve patients revealed consistent results.
IBD patients were more likely to develop psoriasis compared to non-IBD subjects, including younger patients at an elevated risk regardless of TNF inhibitor use. This advocates the interplay between IBD and psoriasis; thus, inspection of cutaneous manifestation and dermatological consultation may be helpful in IBD patients at risk.
新出现的数据表明,炎症性肠病(IBD)和银屑病相关,它们具有共同的遗传易感性和免疫机制。然而,与普通人群相比,IBD 患者患银屑病的具体风险数据有限。
我们研究了 IBD 患者与无 IBD 的对照组相比发生银屑病的风险。
使用韩国国家健康保险数据库,将 2005 年至 2008 年间诊断为克罗恩病(CD)或溃疡性结肠炎(UC)的患者按年龄和性别与 2003 年至 2018 年的非 IBD 对照组 1:4 匹配。IBD 患者的定义是结合国际疾病分类第 10 次修订版代码和至少一种 IBD 特异性药物的处方。还确定了疾病表型,包括银屑病严重程度和银屑病关节炎。我们调查了 2009 年至 2018 年新诊断的银屑病。使用多变量 Cox 回归模型评估银屑病的发生率和风险。进行了年龄和性别亚组分析以及不使用肿瘤坏死因子(TNF)抑制剂的患者的敏感性分析。
在近十年的随访期间,共确定了 20152 名 IBD 患者(14619 名[72.54%]UC 和 5533 名[27.46%]CD)。其中,439 名患者新诊断为银屑病(发病率分别为每 100000 人年 217.68 例和每 100000 人年 228.62 例,UC 和 CD)。IBD 患者的银屑病风险高于匹配对照组(调整后的危险比,aHR,2.95,95%置信区间,CI,2.60-3.33)。此外,年龄<30 岁的 IBD 患者风险增加(aHR 3.35,95%CI 2.58-4.35),这种趋势在所有银屑病表型中均保持不变。对 TNF 抑制剂初治患者的敏感性分析显示出一致的结果。
与非 IBD 患者相比,IBD 患者更易患银屑病,包括 TNF 抑制剂使用与否,年轻患者的风险增加。这表明 IBD 和银屑病之间存在相互作用;因此,对有风险的 IBD 患者进行皮肤表现检查和皮肤科咨询可能会有所帮助。