Abstract
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.
Original language | English (US) |
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Journal | Journal of Investigative Dermatology |
DOIs | |
State | Accepted/In press - 2025 |
Funding
This research was funded by the Science Committee of the Ministry of Science and Higher Education of the Republic of Kazakhstan (grant numbers AP19675503 and AP13068072 to ZM) and Leo Foundation Research Award LF-OC-23-001288 to ICLP. We appreciate the invaluable core support from the Skin Biology and Diseases Resource-based Center (P30 AR075049) and assistance from the Rush University Genomics and Microbiome Core facility. ICLP is the guarantor for this work. Conceptualization: ICLP, ZM; Data Curation: ZR, AK, MD, ZJ, KC, ZM; Funding Acquisition: ICLP, ZM; Investigation: ZM, AK, ZR, SMR, NK, YK, RS, MD, MN, KK, ERD, LC; Methodology: ICLP, ZM, ZR, SMR, AK; Project Administration: ICLP, ZM; Resources: KMD, YO, SSei, SK, SSer, AN, YA, SJG, RVK, AK; Supervision: ICLP, ZM; Visualization: AK, ZR, ZM; Writing - Original Draft Preparation: ZM; Writing - Review and Editing: ICLP, ZM This research has been funded by the Science Committee of the Ministry of Science and Higher Education of the Republic of Kazakhstan Grant No. AP19675503 and AP13068072 to Z.M. and Leo Foundation Research Award LF-OC-23-001288 to I.C.L.P.
Keywords
- Autoimmunity
- Immunology
- Microbiome
- Vitiligo
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Dermatology
- Cell Biology