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Vitiligo and chronic autoimmune thyroiditis.

Authors :
Sandru, Florica
Carsote, Mara
Albu, Simona Elena
Dumitrascu, Mihai Cristian
Valea, Ana
Source :
Journal of Medicine & Life; Mar/Apr2021, Vol. 14 Issue 2, p127-130, 4p
Publication Year :
2021

Abstract

Vitiligo, the discoloration of the skin, has different autoimmune mechanisms reflected by many biomarkers as shown by skin histology, staining for CD4 and CD8 T lymphocytes, chemokine ligand 9 or circulating cytokines such as interleukin (IL)-1 beta, interferon (IFN)-gamma, transforming growth factor (TGF)-beta, antibodies, markers of oxidative stress, chemokines, and others. In this narrative review, we aim to overview vitiligo in relationship with chronic autoimmune thyroiditis. Regarding vitiligo, more than 50 different genetic loci have been associated with this disease, and the heritability is high. There is a 20% risk of an environmental connection which may also act as a trigger; moreover, the association with human leukocyte antigen (HLA) expression is well recognized. The specific lesions display CD8+ tissue-resident memory T cells as continuous key activators of melanocytes. The association with chronic thyroiditis is based on common autoimmune background and excessive reactive oxygen species that destroy melanocytes and thyrocytes (oxidative stress hypothesis) with thyroxine and melanin as target molecules, thus sharing a common origin: tyrosine. Moreover, common epigenetic anomalies or mutations of the Forkhead transcription factor D3 (FOXD3) have been described. Since vitiligo affects up to 1-2% of the population worldwide and 34% of patients have positive thyroid antibodies, apart from common autoimmunity background and oxidative stress toxicity, the association is clinically relevant for different practitioners. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1844122X
Volume :
14
Issue :
2
Database :
Complementary Index
Journal :
Journal of Medicine & Life
Publication Type :
Academic Journal
Accession number :
150905406
Full Text :
https://doi.org/10.25122/jml-2019-0134