Long-term risk of incident psoriasis in patients with irritable bowel syndrome: a large-scale prospective cohort study

银屑病 医学 肠易激综合征 前瞻性队列研究 危险系数 内科学 队列研究 入射(几何) 比例危险模型 累积发病率 队列 置信区间 银屑病面积及严重程度指数 共病 流行病学 优势比 风险评估 疾病严重程度 低风险 生命银行 相对风险 弗雷明翰风险评分
作者
Yuting Qiu,Yesheng Zhou,Si Liu,Qian Zhang,Shutian Zhang,Jing Wu,Shengtao Zhu,Shanshan Wu
出处
期刊:Journal of Global Health [Edinburgh University Global Health Society]
卷期号:16: 04140-04140
标识
DOI:10.7189/jogh.16.04140
摘要

Background: While irritable bowel syndrome (IBS) and psoriasis share some pathophysiological features, it remains unclear whether they are associated with one another. Therefore, we aimed to investigate the long-term risk of incident psoriasis in a large prospective cohort of patients with IBS. Methods: We retrieved data on 437,170 participants from the UK Biobank without psoriasis at baseline. Using ICD-10 codes, we classified these participants into IBS and non-IBS groups based on recruitment status and assessed them for incident psoriasis at follow-ups as the primary outcome. We used multivariable Cox proportional hazards models to estimate adjusted hazard ratios (HRs) and 95% confidence intervals (CIs). Results: We identified 21,748 (5.0%) IBS patients among the 437,170 participants. There were 4325 (1.0%) incident psoriasis cases during a median follow-up period of 14.4 years, amounting to a cumulative incidence of 0.88% (95% CI = 0.73-1.02) in the IBS group vs. 0.69% (95% CI = 0.66-0.72) in the non-IBS group. Compared with non-IBS patients, patients with IBS had a 35.0% higher risk of developing psoriasis (HR = 1.35; 95% CI = 1.19-1.52). In subgroup analyses, a higher psoriasis risk associated with IBS was generally observed across age, sex, Townsend deprivation index, smoking status, non-steroidal anti-inflammatory drug use, C-reactive protein, and polygenic risk score of psoriasis subgroups. Conclusions: The IBS patients in our sample had an increased long-term risk of incident psoriasis. This finding highlights the importance of monitoring psoriasis in IBS patients and suggests a potential shared pathophysiological mechanism between the two conditions which may inform future preventive and therapeutic strategies.
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