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ApaI, BsmI and TaqI VDR gene polymorphisms in association with multiple sclerosis in Slovaks.

Authors :
Čierny, Daniel
Michalik, Jozef
Škereňová, Mária
Kantorová, Ema
Sivák, Štefan
Javor, Juraj
Kurča, Egon
Dobrota, Dušan
Lehotský, Ján
Source :
Neurological Research; Aug2016, Vol. 38 Issue 8, p678-684, 7p
Publication Year :
2016

Abstract

Objective: Vitamin D acts through vitamin D receptor (VDR) and has promising beneficial effects in the development and progression of multiple sclerosis (MS). The purpose of our study was to investigate the possible association of the VDR gene polymorphisms ApaI, BsmI and TaqI with the MS susceptibility and with the rate of disease disability progression in the Central European Slovak population. Methods: The allele and genotype variants of ApaI, TaqI and BsmI VDR gene polymorphisms were analysed in 270 clinically diagnosed MS patients and 303 healthy controls. Genotyping was performed by polymerase chain reaction and restriction analysis. Patients were stratified by the rate of disease disability progression using MSSS scores. Results: By logistic regression analysis, we revealed that genotype BB (AA) of BsmI VDR gene polymorphism is decreasing the risk of MS (BB (AA) vs Bb (AG) + bb (GG); OR = 0.59, 95% CI = 0.39–0.90, p<subscript>log</subscript> = 0.014). We did not identify any association of ApaI and TaqI polymorphisms neither with MS development nor with the disease progression. Discussion: We showed for the first time that BsmI genotype BB (AA) is associated with the decreased susceptibility to MS in Slovak population. We propose the BsmI gene polymorphism to be one of the important genetic markers in evaluation of the risk of MS. However, our data suggest that VDR gene polymorphisms ApaI, BsmI and TaqI are not useful in the prediction of disease disability progression rate in MS in Slovaks. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01616412
Volume :
38
Issue :
8
Database :
Supplemental Index
Journal :
Neurological Research
Publication Type :
Academic Journal
Accession number :
118094561
Full Text :
https://doi.org/10.1080/01616412.2016.1200287