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

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    Author
    Akl, Jennifer
    Lee, Solam
    Ju, Hyun Jeong
    Parisi, Rosa
    Kim, Ji Yoon
    Jeon, Jae Joon
    Heo, Yeon-Woo
    Eleftheriadou, Viktoria
    Hamzavi, Iltefat
    Griffiths, Christopher E M
    Ashcroft, Darren M
    Mysore, Venkataram
    Gupta, Somesh
    Parsad, Davinder
    Lim, Henry
    Bae, Jung Min
    Ezzedine, Khaled
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    Affiliation
    Université Paris-Est Créteil Val de Marne-Université; Yonsei University Wonju College of Medicine; The Catholic University of Korea; University of Manchester; Walsall Healthcare NHS Trust; The Royal Wolverhampton NHS Trust; Henry Ford Health; King's College Hospital; Rajiv Gandhi University of Health Sciences; All India Institute of Medical Sciences; Chandigarh Postgraduate Institute of Medical Education and Research
    Publication date
    2024-06
    Subject
    Dermatology
    
    Metadata
    Show full item record
    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.
    Citation
    Akl J, Lee S, Ju HJ, Parisi R, Kim JY, Jeon JJ, Heo YW, Eleftheriadou V, Hamzavi I, Griffiths CEM, Ashcroft DM, Mysore V, Gupta S, Parsad D, Lim H, Bae JM, Ezzedine K; Global Vitiligo Atlas. Estimating the burden of vitiligo: a systematic review and modelling study. Lancet Public Health. 2024 Jun;9(6):e386-e396.
    Type
    Article
    Handle
    http://hdl.handle.net/20.500.14200/4224
    DOI
    10.1016/S2468-2667(24)00026-4
    PMID
    38552651
    Journal
    The Lancet Public Health
    Publisher
    Elsevier
    ae974a485f413a2113503eed53cd6c53
    10.1016/S2468-2667(24)00026-4
    Scopus Count
    Collections
    Dermatology

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