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Association of genetic variants of the vitamin D receptor gene with vitiligo in a tertiary care center in a Saudi population: a case-control study
Vitiligo is a common cutaneous disorder of the skin and hair caused by a systemic depigmentation disorder that affects 1% of the population or less due to its onset in early adulthood. Meta-analyses have documented a linkage between vitiligo and the vitamin D receptor ( ) gene. Investigate the relat...
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Published in: | Annals of Saudi medicine 2022-03, Vol.42 (2), p.96-106 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Vitiligo is a common cutaneous disorder of the skin and hair caused by a systemic depigmentation disorder that affects 1% of the population or less due to its onset in early adulthood. Meta-analyses have documented a linkage between vitiligo and the vitamin D receptor (
) gene.
Investigate the relationship between the ApaI, BsmI, FokI and TaqI genetic variants in the
gene with vitiligo in a Saudi population.
Case-control.
Single tertiary care center.
The case-control study was carried out between January 2015-December 2015 in Saudi vitiligo patients and healthy controls.
genetic variants or polymorphisms (ApaI, BsmI, FokI and TaqI) were genotyped by polymerase chain reaction-restriction fragment length analysis followed by 3% agarose gel electrophoresis. Applicable statistical methods were used to assess relationships between vitiligo cases and controls.
Effect of genotype distribution among four single nucleotide polymorphisms.
152 vitiligo (median [IQR] 23 [19] years) patients and 159 healthy controls (45 [28.5] years).
We found an association of vitiligo with ApaI and BsmI polymorphisms ( |
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ISSN: | 0256-4947 0975-4466 |
DOI: | 10.5144/0256-4947.2022.96 |