Title of article
The influence of combined genotypes of the HLADRB1*1501 and CD24 single nucleotide polymorphism on disease severity of Iranian multiple sclerosis patients.
Author/Authors
Ghlichnia، Hossein Ali نويسنده Department of Neurology, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran. AND Department of Neurogenetics, Iranian Center of Neurological Research, Tehran, Iran. Ghlichnia, Hossein Ali , Kollaee، Abolghasem نويسنده Department of Neurogenetics, Iranian Center of Neurological Research, Tehran, Iran. AND Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran. Kollaee, Abolghasem , Gaffarpoor، Majid نويسنده Department of Neurogenetics, Iranian Center of Neurological Research, Tehran, Iran. Gaffarpoor, Majid , Movafagh، Abolfazl نويسنده Medical Genetics Department, Shaheed Beheshti University of Medical Sciences , , Ghlichnia، Babak نويسنده Department of Neurogenetics, Iranian Center of Neurological Research, Tehran, Iran. Ghlichnia, Babak , Zamani، Mahdi نويسنده ,
Issue Information
ماهنامه با شماره پیاپی 0 سال 2014
Pages
6
From page
418
To page
423
Abstract
Multiple Sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system. It is a clinically heterogeneous disorder especially in terms of disease severity. Current investigations suggest that genes and gene-gene interactions not only influence on susceptibility to MS but also affect the disease severity. In this study, we investigated the contribution of the HLADRB1*1501 allele and single nucleotide polymorphism (SNP) in CD24 gene and also combined genotypes of the HLADRB1*1501 and CD24 SNP to disease severity in Iranian MS patients. We have reported previously that the HLA- DRB1*1501 allele and the CD24v/v genotype associated with disease susceptibility and some other studies proposed that HLA-DRB1*1501 allele be associated with MS severity. In this study, the results showed a significant difference in the Multiple Sclerosis Severity Score (MSSS) of the nine different genotypes (F=2.838, P=0.007). Subsequent analysis revealed a statistically significant difference in the MSSS between the MS patients who were carriers of HLA-DRB1*1501/1501 and those who were not carriers of HLA-DRB1*1501/1501 genotypes (P=0.04). Moreover, the MS patients carrying combined genotypes of the HLA- DRB1*1501/x-CD24 v/v had statistically severe disease than the patients who did not carry the HLA- DRB1*1501- CD24 v/v (P=0.047). In conclusion, our findings suggest that, HLA-DRB1*1501/1501 and bigenic genotypes of the HLA- DRB1*1501/x- CD24 v/v may influence on disease severity in Iranian MS patients.
Journal title
Acta Medica Iranica
Serial Year
2014
Journal title
Acta Medica Iranica
Record number
2386849
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