PDCD1 Single Nucleotide Polymorphisms in Iranian Patients With Juvenile Idiopathic Arthritis

Juvenile idiopathic arthritis (JIA) is a clinically heterogeneous cluster of complex diseases, in which both the genetic and environmental factors seem to play a role in the development of the disease. The current study aims to assess the association of programmed cell death 1 (PDCD1, also called PD-1) gene variants with JIA vulnerability in Iranian population. In this case-control association study, we investigated a group of 50 Iranian patients with JIA in comparison with 202 healthy controls and evaluated the frequency of alleles, genotypes, and haplotypes of PDCD1 single-nucleotide polymorphisms (SNPs), comprising PD-1.1 G/A, PD-1.3 G/A and PD-1.9 C/T, using PCR-RFLP method. Both the allelic and genotype frequencies of PD-1.1, PD-1.3 and PD-1.9 were similar in two groups of patients and controls. Moreover, no significant difference was observed between the two groups of patients and controls for GGC (PD-1.1 G, PD-1.3 G, PD-1.9 C), GAC (PD-1.1 G, PD-1.3 A, PD-1.9 C), and AGT (PD-1.1 A, PD-1.3 G, PD-1.9 T) haplotypes. Our results did not show any association between PDCD1 SNPs and the development of JIA in Iranian population.

Medienart:

E-Artikel

Erscheinungsjahr:

2017

Erschienen:

2017

Enthalten in:

Zur Gesamtaufnahme - volume:55

Enthalten in:

Acta medica Iranica - 55(2017), 11 vom: 24. Nov., Seite 676-682

Sprache:

Englisch

Beteiligte Personen:

Mahmoudi, Mahdi [VerfasserIn]
Rezaiemanesh, Alireza [VerfasserIn]
Harsini, Sara [VerfasserIn]
Salmaninejad, Arash [VerfasserIn]
Poursani, Shiva [VerfasserIn]
Bahrami, Tayyeb [VerfasserIn]
Ziaee, Vahid [VerfasserIn]
Rezaei, Nima [VerfasserIn]

Themen:

Autoimmunity
Children
Journal Article
Juvenile idiopathic arthritis
PD-1
PDCD1 protein, human
Programmed Cell Death 1 Receptor
Single nucleotide polymorphism

Anmerkungen:

Date Completed 13.06.2018

Date Revised 02.12.2018

published: Print

Citation Status MEDLINE

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM279701756