Association Study of CD226 and CD247 Genes Single Nucleotide Polymorphisms in Iranian Patients with Systemic Sclerosis

CD247 and CD226 play important roles in signaling of lymphocytes. Single nucleotide polymorphisms (SNPs) of genes encoding CD247 and CD226 have been associated with the risk of several autoimmune disorders. This study aimed to evaluate the possible association between CD226 and CD247 genes SNPs and...

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Main Authors: Fatemeh Abbasi, Reza Mansouri, Farhad Gharibdoost, Saeed Aslani, Shayan Mostafaei, Hoda Kavosi, Shiva Poursani, Soheila Sobhani, Mahdi Mahmoudi
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2017-12-01
Series:Iranian Journal of Allergy, Asthma and Immunology
Subjects:
Online Access:https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1482
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author Fatemeh Abbasi
Reza Mansouri
Farhad Gharibdoost
Saeed Aslani
Shayan Mostafaei
Hoda Kavosi
Shiva Poursani
Soheila Sobhani
Mahdi Mahmoudi
author_facet Fatemeh Abbasi
Reza Mansouri
Farhad Gharibdoost
Saeed Aslani
Shayan Mostafaei
Hoda Kavosi
Shiva Poursani
Soheila Sobhani
Mahdi Mahmoudi
author_sort Fatemeh Abbasi
collection DOAJ
description CD247 and CD226 play important roles in signaling of lymphocytes. Single nucleotide polymorphisms (SNPs) of genes encoding CD247 and CD226 have been associated with the risk of several autoimmune disorders. This study aimed to evaluate the possible association between CD226 and CD247 genes SNPs and risk of systemic sclerosis (SSc) in Iranian population. Study participants were 455 SSc patients and 455 age, sex and ethnic -matched healthy individuals. Genotyping of rs2056626 and rs763361 at CD247 and CD226 genes, respectively, was carried out using TaqMan MGB-based allelic discrimination real-time PCR. Neither alleles nor genotypes of both SNPs showed significant association with the risk of SSc. Furthermore, association analysis of the genotypes with clinical manifestations of the disease revealed that rs763361 variants were associated with the forced vital capacity (FVC) in SSc patients. Our results suggest that genetic variants of CD226 and CD247 genes may not be a contributing factor in pathogenesis of SSc in Iranian population.
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spelling doaj.art-cf676d373a5e4ed1bf68f70079e4bcab2022-12-22T01:23:17ZengTehran University of Medical SciencesIranian Journal of Allergy, Asthma and Immunology1735-15021735-52492017-12-011661482Association Study of CD226 and CD247 Genes Single Nucleotide Polymorphisms in Iranian Patients with Systemic SclerosisFatemeh Abbasi0Reza Mansouri1Farhad Gharibdoost2Saeed Aslani3Shayan Mostafaei4Hoda Kavosi5Shiva Poursani6Soheila Sobhani7Mahdi Mahmoudi8Immunology Department, Shahid Sadoughi University of Medical Sciences, Yazd, IranImmunology Department, Shahid Sadoughi University of Medical Sciences, Yazd, IranRheumatology Research Center, Tehran University of Medical Sciences, Tehran, IranRheumatology Research Center, Tehran University of Medical Sciences, Tehran, IranRheumatology Research Center, Tehran University of Medical Sciences, Tehran, IranRheumatology Research Center, Tehran University of Medical Sciences, Tehran, IranRheumatology Research Center, Tehran University of Medical Sciences, Tehran, IranRheumatology Research Center, Tehran University of Medical Sciences, Tehran, IranRheumatology Research Center, Tehran University of Medical Sceinces, Tehran, IranCD247 and CD226 play important roles in signaling of lymphocytes. Single nucleotide polymorphisms (SNPs) of genes encoding CD247 and CD226 have been associated with the risk of several autoimmune disorders. This study aimed to evaluate the possible association between CD226 and CD247 genes SNPs and risk of systemic sclerosis (SSc) in Iranian population. Study participants were 455 SSc patients and 455 age, sex and ethnic -matched healthy individuals. Genotyping of rs2056626 and rs763361 at CD247 and CD226 genes, respectively, was carried out using TaqMan MGB-based allelic discrimination real-time PCR. Neither alleles nor genotypes of both SNPs showed significant association with the risk of SSc. Furthermore, association analysis of the genotypes with clinical manifestations of the disease revealed that rs763361 variants were associated with the forced vital capacity (FVC) in SSc patients. Our results suggest that genetic variants of CD226 and CD247 genes may not be a contributing factor in pathogenesis of SSc in Iranian population.https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1482CD226CD247Single nucleotide polymorphismSystemic sclerosis
spellingShingle Fatemeh Abbasi
Reza Mansouri
Farhad Gharibdoost
Saeed Aslani
Shayan Mostafaei
Hoda Kavosi
Shiva Poursani
Soheila Sobhani
Mahdi Mahmoudi
Association Study of CD226 and CD247 Genes Single Nucleotide Polymorphisms in Iranian Patients with Systemic Sclerosis
Iranian Journal of Allergy, Asthma and Immunology
CD226
CD247
Single nucleotide polymorphism
Systemic sclerosis
title Association Study of CD226 and CD247 Genes Single Nucleotide Polymorphisms in Iranian Patients with Systemic Sclerosis
title_full Association Study of CD226 and CD247 Genes Single Nucleotide Polymorphisms in Iranian Patients with Systemic Sclerosis
title_fullStr Association Study of CD226 and CD247 Genes Single Nucleotide Polymorphisms in Iranian Patients with Systemic Sclerosis
title_full_unstemmed Association Study of CD226 and CD247 Genes Single Nucleotide Polymorphisms in Iranian Patients with Systemic Sclerosis
title_short Association Study of CD226 and CD247 Genes Single Nucleotide Polymorphisms in Iranian Patients with Systemic Sclerosis
title_sort association study of cd226 and cd247 genes single nucleotide polymorphisms in iranian patients with systemic sclerosis
topic CD226
CD247
Single nucleotide polymorphism
Systemic sclerosis
url https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1482
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