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Indian journal of dermatology · 2022

Novel Association between STAT3 Gene Variant and Vitiligo: A Case-Control Study.

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Venkatesh Vaibhav, Mendez Deena C, Rajashekar T S, Balakrishna Sharath

Аннотация

BACKGROUND: Vitiligo is an autoimmune disorder involving inflammatory damage to melanocytes. STAT3 genetic variant (rs744166 T > C) increases inflammatory signaling via JAK/STAT pathway.

AIM: The purpose of this study was to check whether this translates into an association between vitiligo and STAT3 gene variant (rs744166 T > C).

MATERIALS AND METHODS: This is a case-control study. A total of 56 vitiligo patients and 90 healthy, age and gender-matched volunteers were recruited for the study. The STAT3 gene variant (rs744166 T > C) was genotyped using the restriction fragment length polymorphism method.

RESULTS: The frequency of the minor allele 'C' was higher in vitiligo patients (72.3%) than in healthy volunteers (57.8%). The difference between the two groups was statistically significant (P = 0.006; OR = 1.9 with 95% CI). The genotypic variant showed the highest association with vitiligo in the dominant model (P = 0.001).

CONCLUSION: This study shows that the STAT3 gene variant (rs744166 T > C) is associated with vitiligo. This observation underlines the importance of the JAK/STAT signaling pathway in vitiligo pathogenesis.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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