炎症性肠病患者银屑病的发病率:一项基于全国人群的匹配队列研究

Dermatology (Basel, Switzerland) Pub Date : 2021-01-01 Epub Date: 2021-02-08 DOI:10.1159/000514030
Jung Min Moon, Jin Yong Lee, Seong-Joon Koh, Hyunsun Park, Sungchan Kang, Hosim Soh, Hyun Jung Lee, Jong Pil Im, Joo Sung Kim
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引用次数: 9

摘要

背景:新出现的数据表明炎症性肠病(IBD)和牛皮癣是相关的,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患者牛皮癣风险的具体数据有限。目的:研究IBD患者与非IBD对照组相比发生银屑病的风险。方法:使用韩国国民健康保险数据库,2005年至2008年期间诊断为克罗恩病(CD)或溃疡性结肠炎(UC)的患者与2003年至2018年期间诊断为非ibd的患者年龄和性别匹配1:4。IBD患者通过结合国际疾病分类第10版修订代码和至少一种IBD特异性药物处方来定义。疾病表型,包括银屑病严重程度和银屑病关节炎,也被确定。我们调查了2009年至2018年新诊断的牛皮癣。采用多变量Cox回归模型评估牛皮癣的发病率和风险。对年龄和性别进行亚组分析,并对肿瘤坏死因子(TNF) inhibitor-naïve患者进行敏感性分析。结果:在近十年的随访中,发现了20,152例IBD患者(14,619例[72.54%]UC和5,533例[27.46%]CD)。其中新诊断牛皮癣患者439例(UC和CD的发病率分别为217.68 / 10万人-年和228.62 / 10万人-年)。IBD患者患牛皮癣的风险高于匹配对照组(校正风险比,aHR, 2.95, 95%可信区间,CI, 2.60-3.33)。结论:与非IBD患者相比,IBD患者更容易发生牛皮癣,包括年轻患者,无论是否使用TNF抑制剂,其风险均升高。这表明IBD与牛皮癣之间存在相互作用;因此,检查皮肤表现和皮肤科会诊可能对IBD高危患者有帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Incidence of Psoriasis in Patients with Inflammatory Bowel Disease: A Nationwide Population-Based Matched Cohort Study.

Background: 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.

Objective: We investigated the risk of developing psoriasis in IBD patients compared to controls without IBD.

Methods: 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.

Results: 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.

Conclusions: 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.

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