Nigro Alexandra, Osman Alim, Suryadevara Pavan, Cices Ahuva
Department of Dermatology, Eastern Virginia Medical School, Norfolk, Virginia, 23510, USA.
Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York City, New York, 10029, USA.
Arch Dermatol Res. 2025 Jan 8;317(1):201. doi: 10.1007/s00403-024-03679-6.
Vitiligo is a chronic autoimmune skin condition characterized by depigmentation due to the destruction of melanocytes. Recent research has identified potential links between vitiligo and alterations in both the gut and skin microbiomes. This systematic review aims to explore these microbiome changes and their potential role in the onset and progression of vitiligo. A comprehensive search of the PubMed, Medline (OVID), and Web of Science databases was conducted to identify studies examining the gut and/or skin microbiota in vitiligo patients. A total of six studies were included in the qualitative analysis. Data extracted included study type, patient demographics, microbiome sampling methods, bacterial diversity, and bacterial ratios. The studies were assessed using the Methodological Index for Non-Randomized Studies (MINORS) scale. The results revealed inconsistent findings regarding microbial diversity in vitiligo patients. Some studies observed decreased α-diversity in the gut microbiome, while others found an increase, particularly in patients with longer disease duration. An increased Firmicutes-to-Bacteroidetes ratio (higher levels of Firmicutes bacteria compared to Bacteroidetes) was noted in several studies, suggesting a dysbiotic gut microbiome. In the skin microbiome, similar trends of dysbiosis were observed, with alterations in bacterial diversity between lesional and non-lesional skin. The findings indicate that gut and skin microbiome changes may play a role in the pathogenesis of vitiligo. However, the data remain inconclusive due to variability in methodologies and sample sizes. Further research is needed to elucidate the clinical relevance of microbiome alterations in vitiligo, with a focus on controlling external factors such as diet and lifestyle.
白癜风是一种慢性自身免疫性皮肤病,其特征是由于黑素细胞遭到破坏而出现色素脱失。最近的研究已经确定了白癜风与肠道和皮肤微生物群变化之间的潜在联系。本系统综述旨在探讨这些微生物群变化及其在白癜风发病和进展中的潜在作用。我们对PubMed、Medline(OVID)和Web of Science数据库进行了全面检索,以识别研究白癜风患者肠道和/或皮肤微生物群的研究。共有六项研究纳入了定性分析。提取的数据包括研究类型、患者人口统计学信息、微生物群采样方法、细菌多样性和细菌比例。使用非随机研究方法学指数(MINORS)量表对这些研究进行评估。结果显示,关于白癜风患者微生物多样性的研究结果并不一致。一些研究观察到肠道微生物群的α多样性降低,而另一些研究则发现有所增加,尤其是病程较长的患者。几项研究指出,厚壁菌门与拟杆菌门的比例增加(厚壁菌门细菌水平高于拟杆菌门),这表明肠道微生物群存在失调。在皮肤微生物群中,也观察到了类似的失调趋势,病变皮肤和非病变皮肤之间的细菌多样性有所改变。这些发现表明,肠道和皮肤微生物群的变化可能在白癜风的发病机制中起作用。然而,由于方法和样本量的差异,数据仍然没有定论。需要进一步研究以阐明白癜风中微生物群改变的临床相关性,重点是控制饮食和生活方式等外部因素。