Literature DB >> 25319953

HLA-DRA is associated with Parkinson's disease in Iranian population.

J Jamshidi1, A Movafagh, B Emamalizadeh, A Zare Bidoki, A Manafi, S Ghasemi Firouzabadi, G-A Shahidi, S Kazeminasab, P Petramfar, A Fazeli, M Motallebi, S A Mortazavi-Tabatabaei, A Kowsari, Z Jafarian, H Darvish.   

Abstract

The rs3129882, a noncoding variant in HLA-DR, was found to be associated with Parkinson's disease (PD) using several genome-wide association studies. The aim of this replication study was to explore the relationship between this variant and PD in Iranian population. Genomic DNA was extracted from peripheral blood samples, and the rs3129882 SNP was genotyped using a PCR-RFLP method in 520 PD patients and 520 healthy Iranian controls. Significant differences were found in allele frequencies between patients and controls (χ(2) = 4.64, P = 0.031). Under additive and dominant models, the association of the SNP with PD risk is significant, where the A allele was observed to be protective. The results suggest that rs3129882 polymorphism may be a risk factor for PD in Iranian. This is the first study reporting such an association in this population. More replication studies are needed to confirm this data.
© 2014 John Wiley & Sons Ltd.

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Year:  2014        PMID: 25319953     DOI: 10.1111/iji.12151

Source DB:  PubMed          Journal:  Int J Immunogenet        ISSN: 1744-3121            Impact factor:   1.466


  10 in total

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4.  The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population.

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  10 in total

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