作为银屑病关节炎风险因素的银屑病多发病:基于人群的研究

IF 4.7 2区 医学 Q1 RHEUMATOLOGY
Paras Karmacharya, Rikesh Chakradhar, Cassondra A Hulshizer, Tina M Gunderson, Alexis Ogdie, John M Davis Iii, Kerry Wright, Megha M Tollefson, Alí Duarte-García, Delamo Bekele, Hilal Maradit-Kremers, Cynthia S Crowson
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引用次数: 0

摘要

目的研究银屑病多发病及其与 PsA 发展的关系:利用罗切斯特流行病学项目开展了一项回顾性队列研究。通过人工病历审查确定了基于人群的银屑病发病率队列(2000-2009 年)和患病率队列(2010 年 1 月 1 日)。此外,还确定了一个无银屑病患者队列(对比者)(年龄、性别和县级匹配度为 1:1)。发病率的定义是:在过去五年内,发病时间相隔≥30 天,且发病时间相隔≥2 个临床分类软件代码。PsA 采用银屑病关节炎分类标准(CASPAR)定义。采用χ2检验和秩和检验比较发病率,并采用年龄、性别和种族调整后的Cox模型研究银屑病基线发病率与PsA发展的关系:在817名银屑病患者中,平均年龄为45.2岁,52.0%为女性,82.0%为中度/重度银屑病。在发病的银屑病患者与对照组患者之间未发现多种疾病的差异。然而,在 1,088 名发病的银屑病患者中,与 1,086 名对照组患者相比,多病症的发病率明显更高(发病率≥2 和发病率≥5 分别为 OR : 1.35 和 OR : 1.48)。在中位 13.3 年的随访中,23 名患者(15 年累计发病率:2.9%)出现了 PsA。多病(≥2种疾病)与PsA发病风险高3倍相关:结论:与普通人群相比,银屑病流行组群中的多病症更为常见,但非发病组群中的多病症更为常见,这表明银屑病患者可能会加速多病症的发展。此外,银屑病发病时的多病症会显著增加罹患PsA的风险,这凸显了监测多病症银屑病患者是否罹患PsA的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimorbidity in psoriasis as a risk factor for psoriatic arthritis: a population-based study.

Objectives: To examine multimorbidity in psoriasis and its association with the development of psoriatic arthritis (PsA).

Methods: A retrospective cohort study was performed using the Rochester Epidemiology Project. Population-based incidence (2000-09) and prevalence (1 January 2010) cohorts of psoriasis were identified by manual chart review. A cohort of individuals without psoriasis (comparators) were identified (1:1 matched on age, sex and county). Morbidities were defined using two or more Clinical Classification Software codes ≥30 days apart within prior 5 years. PsA was defined using ClASsification of Psoriatic ARthritis (CASPAR) criteria. χ2 and rank-sum tests were used to compare morbidities, and age-, sex- and race-adjusted Cox models to examine the association of baseline morbidities in psoriasis with development of PsA.

Results: Among 817 incident psoriasis patients, the mean age was 45.2 years with 52.0% females, and 82.0% moderate/severe psoriasis. No multimorbidity differences were found between incident psoriasis patients and comparators. However, in the 1088 prevalent psoriasis patients, multimorbidity was significantly more common compared with 1086 comparators (odds ratio 1.35 and 1.48 for two or more and five or more morbidities, respectively). Over a median 13.3-year follow-up, 23 patients (cumulative incidence: 2.9% by 15 years) developed PsA. Multimorbidity (two or more morbidities) was associated with a 3-fold higher risk of developing PsA.

Conclusion: Multimorbidity was more common in the prevalent but not incident cohort of psoriasis compared with the general population, suggesting that patients with psoriasis may experience accelerated development of multimorbidity. Moreover, multimorbidity at psoriasis onset significantly increased the risk of developing PsA, highlighting the importance of monitoring multimorbid psoriasis patients for the development of PsA.

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来源期刊
Rheumatology
Rheumatology 医学-风湿病学
CiteScore
9.40
自引率
7.30%
发文量
1091
审稿时长
2 months
期刊介绍: Rheumatology strives to support research and discovery by publishing the highest quality original scientific papers with a focus on basic, clinical and translational research. The journal’s subject areas cover a wide range of paediatric and adult rheumatological conditions from an international perspective. It is an official journal of the British Society for Rheumatology, published by Oxford University Press. Rheumatology publishes original articles, reviews, editorials, guidelines, concise reports, meta-analyses, original case reports, clinical vignettes, letters and matters arising from published material. The journal takes pride in serving the global rheumatology community, with a focus on high societal impact in the form of podcasts, videos and extended social media presence, and utilizing metrics such as Altmetric. Keep up to date by following the journal on Twitter @RheumJnl.
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