Psoriasis in People With Skin of Color: An Evidence-Based Update

IF 3.5 4区 医学 Q1 DERMATOLOGY
Maria-Angeliki Gkini, Mio Nakamura, Andrew F. Alexis, Angela Londoño-Garcia, Peter C. M. van de Kerkhof, Nejib Doss, Christopher E. M. Griffiths, Bridget Kaufman, Christine E. Kleyn, Mark Lebwohl, Jan S. Redfern, Junko Takeshita, Murlidhar Rajagopalan, Mahira H. El Sayed
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Abstract

Variations in epidemiology, pathophysiology, genetics, clinical presentation, management, quality of life (QoL) impact, and access to care and research exist globally across the spectrum of individuals with psoriasis. This article aims to provide an evidence-based update on the characteristics of psoriasis in individuals with skin of color (SOC), a population in which psoriasis data have historically been limited. A literature search was conducted from January 2018 until August 2023 in Pubmed/MEDLINE/Cochrane Library and identified studies with I-III level of evidence using Oxford Centre for Evidence-Based Medicine recommendations. Multiple factors (including biological and non-biological) contribute to differences in clinical features and therapeutic nuances in patient populations with SOC. The prevalence of plaque psoriasis is lower in people with SOC but tends to be more severe. People with SOC are less likely to receive biologic treatment. Although the QoL impact of psoriasis is worse in populations with SOC than in White populations, more research is needed to elucidate variations in presentation and impact across diverse populations. An important limitation of this study is that ethnicity, race, and SOC have not been defined universally or used consistently in the literature. Available evidence provides limited information on populations with SOC outside North America, which limits generalizability across global populations. Furthering our understanding of psoriasis in individuals with SOC is crucial to improving patient care outcomes for diverse patient populations worldwide.

Abstract Image

有色人种的牛皮癣:基于证据的最新进展。
在流行病学、病理生理学、遗传学、临床表现、管理、生活质量(QoL)影响以及获得护理和研究方面,牛皮癣患者在全球范围内存在差异。本文旨在为有色皮肤(SOC)患者的牛皮癣特征提供循证更新,这一人群的牛皮癣数据历来有限。从2018年1月至2023年8月,在Pubmed/MEDLINE/Cochrane图书馆进行了文献检索,并根据牛津循证医学中心的建议确定了I-III级证据的研究。多种因素(包括生物和非生物因素)导致SOC患者群体的临床特征和治疗差异。斑块型银屑病的患病率在SOC患者中较低,但往往更严重。SOC患者接受生物治疗的可能性较小。虽然牛皮癣对生活质量的影响在SOC人群中比白人人群更差,但需要更多的研究来阐明不同人群中牛皮癣表现和影响的变化。本研究的一个重要局限性是,种族、种族和SOC在文献中没有被普遍定义或一致使用。现有证据提供的关于北美以外SOC种群的信息有限,这限制了在全球种群中的推广。进一步了解SOC患者的牛皮癣对于改善全球不同患者群体的患者护理结果至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.70
自引率
2.80%
发文量
476
审稿时长
3 months
期刊介绍: Published monthly, the International Journal of Dermatology is specifically designed to provide dermatologists around the world with a regular, up-to-date source of information on all aspects of the diagnosis and management of skin diseases. Accepted articles regularly cover clinical trials; education; morphology; pharmacology and therapeutics; case reports, and reviews. Additional features include tropical medical reports, news, correspondence, proceedings and transactions, and education. The International Journal of Dermatology is guided by a distinguished, international editorial board and emphasizes a global approach to continuing medical education for physicians and other providers of health care with a specific interest in problems relating to the skin.
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