{"title":"西方与南亚国家的白癜风和抑郁症:应考虑文化背景。","authors":"Shahnawaz Towheed, Zaakir Hamzavi, Viktoria Eleftheriadou, Khaled Ezzedine","doi":"10.1016/j.jid.2025.09.021","DOIUrl":null,"url":null,"abstract":"<p><p>Reported psychosocial outcomes in vitiligo vary considerably across geographic and cultural contexts, yet no comprehensive review has compared these differences. In this study, we aimed to review the psychological and social impact of vitiligo, with a comparative focus on South Asia and Western countries. In this review, Western countries were defined as Europe, the United States, Canada, and Australia, whereas South Asian countries included India, Pakistan, Bangladesh, Sri Lanka, and Nepal. This narrative review was conducted using PubMed, Scopus, Web of Science, and PsycINFO, including English- and French-language publications from 2000 to 2025. Evidence was categorized across 5 thematic domains: (i) psychological outcomes, (ii) social consequences, (iii) skin phototype and visibility, (iv) health system and policy factors, and (v) cultural and religious frameworks. Psychiatric morbidity was highest in South Asian populations, with depression and anxiety rates reaching up to 60%, compared with 15-30% in European cohorts and 20-30% in North American and Australian samples. Stigma in India was exacerbated by cultural beliefs related to contagion, impurity, karma, and dietary taboos, especially among individuals with darker skin phototypes. Western patients more often reported issues related to self-image and social withdrawal but faced fewer institutional or interpersonal barriers. Future research should prioritize longitudinal and community-based studies to inform interventions that shift vitiligo from a socially disabling condition to a manageable chronic difference.</p>","PeriodicalId":94239,"journal":{"name":"The Journal of investigative dermatology","volume":" ","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Vitiligo and Depression in Western versus South Asian Countries: Cultural Background Should Be Considered.\",\"authors\":\"Shahnawaz Towheed, Zaakir Hamzavi, Viktoria Eleftheriadou, Khaled Ezzedine\",\"doi\":\"10.1016/j.jid.2025.09.021\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Reported psychosocial outcomes in vitiligo vary considerably across geographic and cultural contexts, yet no comprehensive review has compared these differences. In this study, we aimed to review the psychological and social impact of vitiligo, with a comparative focus on South Asia and Western countries. In this review, Western countries were defined as Europe, the United States, Canada, and Australia, whereas South Asian countries included India, Pakistan, Bangladesh, Sri Lanka, and Nepal. This narrative review was conducted using PubMed, Scopus, Web of Science, and PsycINFO, including English- and French-language publications from 2000 to 2025. Evidence was categorized across 5 thematic domains: (i) psychological outcomes, (ii) social consequences, (iii) skin phototype and visibility, (iv) health system and policy factors, and (v) cultural and religious frameworks. Psychiatric morbidity was highest in South Asian populations, with depression and anxiety rates reaching up to 60%, compared with 15-30% in European cohorts and 20-30% in North American and Australian samples. Stigma in India was exacerbated by cultural beliefs related to contagion, impurity, karma, and dietary taboos, especially among individuals with darker skin phototypes. Western patients more often reported issues related to self-image and social withdrawal but faced fewer institutional or interpersonal barriers. Future research should prioritize longitudinal and community-based studies to inform interventions that shift vitiligo from a socially disabling condition to a manageable chronic difference.</p>\",\"PeriodicalId\":94239,\"journal\":{\"name\":\"The Journal of investigative dermatology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.7000,\"publicationDate\":\"2025-10-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of investigative dermatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jid.2025.09.021\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of investigative dermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.jid.2025.09.021","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
据报道,白癜风患者的心理社会结局在不同的地理和文化背景下差异很大,但尚未有全面的综述对这些差异进行比较。在本研究中,我们旨在回顾白癜风的心理和社会影响,并以南亚和西方国家为比较重点。在本综述中,西方国家被定义为欧洲、美国、加拿大和澳大利亚,而南亚国家包括印度、巴基斯坦、孟加拉国、斯里兰卡和尼泊尔。本文使用PubMed、Scopus、Web of Science和PsycINFO进行叙述性回顾,包括2000年至2025年期间的英语和法语出版物。证据分为5个主题领域:(i)心理结果,(ii)社会后果,(iii)皮肤光型和可见度,(iv)卫生系统和政策因素,以及(v)文化和宗教框架。精神疾病发病率在南亚人群中最高,抑郁和焦虑率高达60%,而在欧洲人群中为15-30%,在北美和澳大利亚人群中为20-30%。在印度,与传染病、不洁、因果报应和饮食禁忌有关的文化信仰加剧了耻辱,尤其是在肤色较深的个体中。西方患者更常报告与自我形象和社会退缩有关的问题,但面临较少的制度或人际障碍。未来的研究应优先考虑纵向和基于社区的研究,以告知将白癜风从社会致残状况转变为可控制的慢性差异的干预措施。
Vitiligo and Depression in Western versus South Asian Countries: Cultural Background Should Be Considered.
Reported psychosocial outcomes in vitiligo vary considerably across geographic and cultural contexts, yet no comprehensive review has compared these differences. In this study, we aimed to review the psychological and social impact of vitiligo, with a comparative focus on South Asia and Western countries. In this review, Western countries were defined as Europe, the United States, Canada, and Australia, whereas South Asian countries included India, Pakistan, Bangladesh, Sri Lanka, and Nepal. This narrative review was conducted using PubMed, Scopus, Web of Science, and PsycINFO, including English- and French-language publications from 2000 to 2025. Evidence was categorized across 5 thematic domains: (i) psychological outcomes, (ii) social consequences, (iii) skin phototype and visibility, (iv) health system and policy factors, and (v) cultural and religious frameworks. Psychiatric morbidity was highest in South Asian populations, with depression and anxiety rates reaching up to 60%, compared with 15-30% in European cohorts and 20-30% in North American and Australian samples. Stigma in India was exacerbated by cultural beliefs related to contagion, impurity, karma, and dietary taboos, especially among individuals with darker skin phototypes. Western patients more often reported issues related to self-image and social withdrawal but faced fewer institutional or interpersonal barriers. Future research should prioritize longitudinal and community-based studies to inform interventions that shift vitiligo from a socially disabling condition to a manageable chronic difference.