| Literature DB >> 28317533 |
Richard A Spritz1, Genevieve H L Andersen2.
Abstract
Vitiligo reflects simultaneous contributions of multiple genetic risk factors and environmental triggers. Genomewide association studies have discovered approximately 50 genetic loci contributing to vitiligo risk. At many vitiligo susceptibility loci, the relevant genes and DNA sequence variants are identified. Many encode proteins involved in immune regulation, several play roles in cellular apoptosis, and others regulate functions of melanocytes. Although many of the specific biologic mechanisms need elucidation, it is clear that vitiligo is an autoimmune disease involving a complex relationship between immune system programming and function, aspects of the melanocyte autoimmune target, and dysregulation of the immune response.Entities:
Keywords: Autoimmunity; Gene; Genetic epidemiology; Genetic linkage; Genomewide association study; Vitiligo
Mesh:
Substances:
Year: 2017 PMID: 28317533 PMCID: PMC5362127 DOI: 10.1016/j.det.2016.11.013
Source DB: PubMed Journal: Dermatol Clin ISSN: 0733-8635 Impact factor: 3.478