TY - JOUR
T1 - Escherichia Abundance and Metabolism Align with Vitiligo Disease Activity
AU - Mukhatayev, Zhussipbek
AU - Kovenskiy, Artur
AU - Ren, Ziyou
AU - Rangel, Stephanie M.
AU - Katkenov, Nurlubek
AU - Khuanbai, Yerkhanat
AU - Shivde, Rohan
AU - Daniel, Moriel
AU - Dellacecca, Emilia R.
AU - Cedercreutz, Kettil
AU - Ostapchuk, Yekaterina
AU - Nurgozhina, Ayaulum
AU - Chulenbayeva, Laura
AU - Nurgaziyev, Madiyar
AU - Jarmukhanov, Zharkyn
AU - Nurlankyzy, Marzhan
AU - Kozhdan, Kamilya
AU - Seidulla, Symbat
AU - Mukhanbetzhanova, Zhanel
AU - Sergazy, Shynggyss
AU - Kozhakhmetov, Samat
AU - Ali, Yasmeen
AU - Daftary, Karishma M.
AU - Green, Stefan J.
AU - Kundu, Roopal V.
AU - Kushugulova, Almagul
AU - Le Poole, I. Caroline
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025
Y1 - 2025
N2 - Vitiligo is a cutaneous autoimmune disorder characterized by progressive depigmentation due to melanocyte destruction by cytotoxic T cells. Genetic factors predispose patients to the disease and are supported by environmental factors that often initiate new disease episodes. We investigated whether disease outcomes were partially defined by pathogenic microbes that drive nutrient deficiency and inflammation. Our study presents the results of research on the diet and gut microbiome composition of patients with vitiligo and healthy controls from Kazakhstan and the United States. Dietary nutrient intake was assessed using the National Institutes of Health–generated Diet History Questionnaire. Patients with active vitiligo exhibit a limited intake of specific fatty acids, amino acids, fiber, and zinc. Disease activity was further characterized by the abundance of Odoribacter and Escherichia in the gut. Metabolic pathway analysis supported the role of the Escherichia genus in disease activity by limiting energy metabolism and amino acid biosynthetic pathways. Disease activity was also associated with elevated circulating proinflammatory cytokines. These findings suggest that nutritional limitations are not compensated by metabolites from the gut microbiome in active disease, potentially leaving room for inflammation and exacerbating vitiligo. The intricate relationship among diet, gut microbiome composition, and disease progression in vitiligo highlights potential avenues for targeted interventions to reduce autoimmune activity and improve patient outcomes.
AB - Vitiligo is a cutaneous autoimmune disorder characterized by progressive depigmentation due to melanocyte destruction by cytotoxic T cells. Genetic factors predispose patients to the disease and are supported by environmental factors that often initiate new disease episodes. We investigated whether disease outcomes were partially defined by pathogenic microbes that drive nutrient deficiency and inflammation. Our study presents the results of research on the diet and gut microbiome composition of patients with vitiligo and healthy controls from Kazakhstan and the United States. Dietary nutrient intake was assessed using the National Institutes of Health–generated Diet History Questionnaire. Patients with active vitiligo exhibit a limited intake of specific fatty acids, amino acids, fiber, and zinc. Disease activity was further characterized by the abundance of Odoribacter and Escherichia in the gut. Metabolic pathway analysis supported the role of the Escherichia genus in disease activity by limiting energy metabolism and amino acid biosynthetic pathways. Disease activity was also associated with elevated circulating proinflammatory cytokines. These findings suggest that nutritional limitations are not compensated by metabolites from the gut microbiome in active disease, potentially leaving room for inflammation and exacerbating vitiligo. The intricate relationship among diet, gut microbiome composition, and disease progression in vitiligo highlights potential avenues for targeted interventions to reduce autoimmune activity and improve patient outcomes.
KW - Autoimmunity
KW - Immunology
KW - Microbiome
KW - Vitiligo
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U2 - 10.1016/j.jid.2025.01.032
DO - 10.1016/j.jid.2025.01.032
M3 - Article
C2 - 39983982
AN - SCOPUS:105000904875
SN - 0022-202X
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
ER -