Estimating the burden of vitiligo: a systematic review and modelling study.

IF 25.4 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Lancet Public Health Pub Date : 2024-06-01 Epub Date: 2024-03-26 DOI:10.1016/S2468-2667(24)00026-4
Jennifer Akl, Solam Lee, Hyun Jeong Ju, Rosa Parisi, Ji Yoon Kim, Jae Joon Jeon, Yeon-Woo Heo, Viktoria Eleftheriadou, Iltefat Hamzavi, Christopher E M Griffiths, Darren M Ashcroft, Venkataram Mysore, Somesh Gupta, Davinder Parsad, Henry Lim, Jung Min Bae, Khaled Ezzedine
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引用次数: 0

Abstract

Background: Vitiligo is a chronic autoimmune disease characterised by depigmented skin patches, which can pose substantial psychosocial challenges particularly in individuals with dark skin tones. Despite its impact on quality of life, there is an absence of standardised global epidemiological data. We sought to address this gap with the present study.

Methods: In this study we did a systematic review and modelling analysis to estimate the global, regional, and national prevalence and incidence of vitiligo. We did a comprehensive search of nine digital libraries (PubMed, Embase, Web of Science, Scientific Electronic Library Online, KCI Korean Journal Database, Russian Science Citation Index, Western Pacific Region Index Medicus, Informit, and Health Research and Development Information Network) from inception up to May 25, 2023. We included cross-sectional or cohort studies reporting the incidence rate or prevalence of vitiligo, or data from which incidence rate or prevalence could be calculated, in the general population of a country or area of a country. Summary estimate data were extracted. A main outcome was to estimate the worldwide, regional, and country-specific lifetime prevalence of vitiligo diagnosed by physicians or dermatologists among the general population and in adults and children (as per age groups defined in included studies). We used a Bayesian hierarchical linear mixed model to estimate prevalence, and calculated number of affected individuals using the UN population structure in 2022. In estimating lifetime prevalence, studies reporting point or period prevalence were excluded. Our other main outcome was to estimate incidence rates of vitiligo, but due to a small number of studies, the data on incidence were presented in a descriptive summary. This study was registered on PROSPERO, CRD42023390433.

Findings: Our search identified 22 192 records, of which 90 studies met our inclusion criteria. Of these studies, six focused on the incidence of vitiligo, 79 reported on the prevalence of vitiligo, and five provided data on both incidence and prevalence. 71 studies reported on lifetime prevalence. In the most recent years studied, incidence rates in the general population ranged from 24·7 cases (95% CI 24·3-25·2) per 100 000 person-years in South Korea in 2019, to 61·0 cases (60·6-61·4) in the USA in 2017. In individual studies, incidence rates showed an increasing trend over the periods studied. The global lifetime prevalence of vitiligo diagnosed by a physician or dermatologist was estimated at 0·36% (95% credible interval [CrI] 0·24-0·54) in the general population (28·5 million people [95% CrI 18·9-42·6]), 0·67% (0·43-1·07) in the adult population (37·1 million adults [23·9-58·9]), and 0·24% (0·16-0·37) in the child population (5·8 million children [3·8-8·9]). Vitiligo prevalence was higher in adults than in children across all regions. Central Europe and south Asia reported the highest prevalence (0·52% [0·28-1·07] and 0·52% [0·33-0·82], respectively, in the general population).

Interpretation: This study highlights the need for standardised epidemiological data collection globally to inform public health policies and improve vitiligo diagnosis and management. Emphasis on the impact on individuals with darker skin tones is crucial to reducing stigma and improving quality of life. Furthermore, our study highlights the need to conduct more research in regions and populations that have been historically under-represented, to effectively address the worldwide burden of vitiligo.

Funding: None.

估算白癜风的负担:系统回顾与模型研究。
背景:白癜风是一种以皮肤色素脱失斑为特征的慢性自身免疫性疾病,会给患者,尤其是肤色较深的患者带来巨大的社会心理挑战。尽管白癜风会影响患者的生活质量,但目前尚缺乏标准化的全球流行病学数据。我们试图通过本研究填补这一空白:在本研究中,我们进行了系统回顾和建模分析,以估算全球、地区和国家的白癜风流行率和发病率。我们对九个数字图书馆(PubMed、Embase、Web of Science、Scientific Electronic Library Online、KCI Korean Journal Database、Russian Science Citation Index、Western Pacific Region Index Medicus、Informit 和 Health Research and Development Information Network)进行了全面检索,检索时间从开始到 2023 年 5 月 25 日。我们纳入了报告一个国家或一个国家地区普通人群中白癜风发病率或流行率的横断面或队列研究,或可计算发病率或流行率的数据。提取了简要估计数据。主要研究结果之一是估算经内科医生或皮肤科医生诊断的白癜风在普通人群、成人和儿童(根据纳入研究中定义的年龄组)中的全球、地区和特定国家的终生发病率。我们采用贝叶斯分层线性混合模型来估算患病率,并根据联合国2022年的人口结构来计算患病人数。在估算终生流行率时,排除了报告点流行率或阶段流行率的研究。我们的另一个主要结果是估算白癜风的发病率,但由于研究数量较少,发病率数据以描述性摘要的形式呈现。本研究已在 PROSPERO 上注册,注册号为 CRD42023390433:我们的搜索发现了 22 192 条记录,其中 90 项研究符合我们的纳入标准。在这些研究中,6 项研究关注白癜风的发病率,79 项研究报告了白癜风的患病率,5 项研究同时提供了发病率和患病率的数据。71项研究报告了终生发病率。在最近几年的研究中,普通人群的发病率从2019年韩国的每10万人年24-7例(95% CI 24-3-25-2)到2017年美国的61-0例(60-6-61-4)不等。在个别研究中,发病率在研究期间呈上升趋势。经内科医生或皮肤科医生诊断的全球白癜风终生患病率估计为:普通人群(2800-500万人[95% CrI 18-9-42-6])0-36%(95%可信区间[CrI] 0-24-0-54),成人人群(3700-100万成人[23-9-58-9])0-67%(0-43-1-07),儿童人群(500-800万儿童[3-8-8-9])0-24%(0-16-0-37)。在所有地区,成人白癜风发病率均高于儿童。中欧和南亚的发病率最高(在普通人群中分别为 0-52% [0-28-1-07] 和 0-52% [0-33-0-82]):这项研究强调了在全球范围内收集标准化流行病学数据的必要性,以便为公共卫生政策提供信息,并改善白癜风的诊断和管理。强调对肤色较深的人的影响对于减少耻辱感和提高生活质量至关重要。此外,我们的研究还强调,有必要在历来代表性不足的地区和人群中开展更多研究,以有效解决白癜风给全世界带来的负担:无。
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
Lancet Public Health
Lancet Public Health Medicine-Public Health, Environmental and Occupational Health
CiteScore
55.60
自引率
0.80%
发文量
305
审稿时长
8 weeks
期刊介绍: The Lancet Public Health is committed to tackling the most pressing issues across all aspects of public health. We have a strong commitment to using science to improve health equity and social justice. In line with the values and vision of The Lancet, we take a broad and inclusive approach to public health and are interested in interdisciplinary research. We publish a range of content types that can advance public health policies and outcomes. These include Articles, Review, Comment, and Correspondence. Learn more about the types of papers we publish.
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