Psoriatic arthritis with psychological comorbidities: an overview of systematic reviews on incidence, prevalence, and geographic disparities.

IF 3.2 3区 医学 Q2 RHEUMATOLOGY
Rheumatology International Pub Date : 2024-11-01 Epub Date: 2024-05-26 DOI:10.1007/s00296-024-05617-1
Juan-Carlos Hernández-Rodríguez, Marta Infante-Cano, Cristina García-Muñoz, Javier Matias-Soto, Javier Martinez-Calderon
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引用次数: 0

Abstract

Systematic reviews and meta-analysis evaluating the prevalence, incidence, and psychological comorbidities of psoriatic arthritis (PsA) are increasing, so it's time to perform an overview of systematic reviews. To summarize the pooled prevalence, incidence, and psychological comorbidities rates of PsA, and to explore possible continent disparities. In this overview of systematic reviews the CINAHL, EMBASE, PsycINFO, and PubMed were searched to October 25, 2023. This overview included systematic reviews with meta-analysis of people with PsA, providing the pooled prevalence or incidence rates of PsA in general, or clinical populations and/or psychological comorbidities. The Preferred Reporting Items for Overviews of Reviews (PRIOR) statement was followed. AMSTAR-2 assessed the quality of reviews. The degree of overlap was calculated using the corrected covered area (CCA). Maps were developed using the location of where primary studies were conducted using DataWrapper App. The protocol was prospectively registered with Open Science Framework registry. Pooled prevalence and incidence rates of PsA or its associated psychological comorbidities in general or specific populations. We also collected locations from the primary studies of the included meta-analyses. Only the assessment of prevalence rates of PsA in people with psoriasis showed slight overlap (CCA = 3.3%). Items 2, 3, 4, 7, 8, 10, 12, and 13 were poorly reported in AMSTAR-2. The pooled prevalence of PsA ranged from 0.13 to 0.15% in the general population, and 15.5% to 19.7% in people with psoriasis. The pooled incidence of PsA ranged from 8.26 to 9.27 cases per 100,000 inhabitants to 0.87 cases in individuals with hidradenitis suppurativa. The pooled prevalence of psychological comorbidities was 11.9-20% for depression, 19-33% anxiety, 38% alexithymia, and 72.9% in poor sleep quality. Only the pooled incidence of depression was assessed with 21.3 per 1000-person year. PsA seems to be prevalent and incident not only in people with psoriasis, but also in general population. Depression and anxiety symptoms may be present in some patients with PsA. Finally, continent disparities exist, and methodological and clinical issues were found, which could be helpful in the future agenda of the epidemiology of PsA.

Abstract Image

伴有心理并发症的银屑病关节炎:关于发病率、流行率和地域差异的系统综述。
评估银屑病关节炎(PsA)患病率、发病率和心理并发症的系统综述和荟萃分析越来越多,因此是时候对系统综述进行概述了。总结PsA的患病率、发病率和心理并发症的汇总情况,并探讨可能存在的大陆差异。在本系统综述中,检索了截至 2023 年 10 月 25 日的 CINAHL、EMBASE、PsycINFO 和 PubMed。本综述包括对PsA患者进行荟萃分析的系统综述,提供了一般PsA或临床人群和/或心理并发症的总体流行率或发病率。研究遵循了 "综述首选报告项目"(PRIOR)声明。AMSTAR-2 评估了综述的质量。使用校正覆盖面积(CCA)计算重叠程度。使用 DataWrapper 应用程序根据主要研究的开展地点绘制地图。研究方案在开放科学框架注册中心进行了前瞻性注册。汇总一般或特定人群中 PsA 或其相关心理并发症的流行率和发病率。我们还收集了纳入荟萃分析的主要研究的地点。只有对银屑病患者 PsA 患病率的评估略有重叠(CCA = 3.3%)。AMSTAR-2的第2、3、4、7、8、10、12和13项报告较少。在普通人群中,PsA 的合计患病率为 0.13% 至 0.15%,在银屑病患者中为 15.5% 至 19.7%。在每 10 万居民中,PsA 的总发病率为 8.26 至 9.27 例,在化脓性扁平苔藓患者中为 0.87 例。心理合并症的汇总发病率为:抑郁 11.9%-20%、焦虑 19%-33%、失眠 38%、睡眠质量差 72.9%。仅评估了抑郁症的总发病率,为每千人年 21.3 例。PsA 似乎不仅在银屑病患者中流行,在普通人群中也有发生。一些 PsA 患者可能会出现抑郁和焦虑症状。最后,研究还发现了大陆差异、方法学和临床问题,这些都有助于今后开展 PsA 流行病学研究。
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来源期刊
Rheumatology International
Rheumatology International 医学-风湿病学
CiteScore
7.30
自引率
5.00%
发文量
191
审稿时长
16. months
期刊介绍: RHEUMATOLOGY INTERNATIONAL is an independent journal reflecting world-wide progress in the research, diagnosis and treatment of the various rheumatic diseases. It is designed to serve researchers and clinicians in the field of rheumatology. RHEUMATOLOGY INTERNATIONAL will cover all modern trends in clinical research as well as in the management of rheumatic diseases. Special emphasis will be given to public health issues related to rheumatic diseases, applying rheumatology research to clinical practice, epidemiology of rheumatic diseases, diagnostic tests for rheumatic diseases, patient reported outcomes (PROs) in rheumatology and evidence on education of rheumatology. Contributions to these topics will appear in the form of original publications, short communications, editorials, and reviews. "Letters to the editor" will be welcome as an enhancement to discussion. Basic science research, including in vitro or animal studies, is discouraged to submit, as we will only review studies on humans with an epidemological or clinical perspective. Case reports without a proper review of the literatura (Case-based Reviews) will not be published. Every effort will be made to ensure speed of publication while maintaining a high standard of contents and production. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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