2016
DOI: 10.4238/gmr.15027966
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Correlation between IL-3 and IL-13 gene polymorphisms in Chinese patients and rheumatoid arthritis

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Cited by 3 publications
(3 citation statements)
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“…One of the commonly examined versions of IL-13 is a single nucleotide polymorphism rs1800925 (-1055 C/T; promoter region). IL-13 rs1800925 has been studied in RA patients; however, no associations have been found between this genetic variant and a susceptibility to the disease in three different studies comprising Chinese and Caucasian populations [ 61 , 62 , 63 , 64 ]. Although stratification analyses in the study by Wang et al revealed that the C allele was associated with RA risk in Chinese patients with erythrocyte sedimentation rate (ESR) < 25.00 [ 64 ].…”
Section: Il-4 and Il-13 Polymorphism In Inflammatory Arthritismentioning
confidence: 99%
“…One of the commonly examined versions of IL-13 is a single nucleotide polymorphism rs1800925 (-1055 C/T; promoter region). IL-13 rs1800925 has been studied in RA patients; however, no associations have been found between this genetic variant and a susceptibility to the disease in three different studies comprising Chinese and Caucasian populations [ 61 , 62 , 63 , 64 ]. Although stratification analyses in the study by Wang et al revealed that the C allele was associated with RA risk in Chinese patients with erythrocyte sedimentation rate (ESR) < 25.00 [ 64 ].…”
Section: Il-4 and Il-13 Polymorphism In Inflammatory Arthritismentioning
confidence: 99%
“…Single nucleotide polymorphisms (SNPs) are the most common genetic variations and if located in the coding regions of genes can result in loss, abrogation or altered function of the downstream protein by causing alterations in amino acid sequences and protein structure [ 28 , 29 ]. IL-13 gene is located on chromosome 5q23.31 and encodes IL-13 cytokine [ 30 ]. Single nucleotide polymorphisms substitution of the nucleotide cytosine (allele C) to thymine (allele T) at the IL-13 rs1800925 (also known as -1111C/T, -1055C/T and -1112C/T) site in the promoter region, results in the binding of nuclear proteins [ 31 ].…”
Section: Introductionmentioning
confidence: 99%
“…HLA loci account for ~50% of the genetic predisposition to RA . The polymorphisms and expression levels of several immune‐related genes, such as TCR‐CD3 ζ gene and IL‐13 gene, could affect the pathogenesis of RA. A few HLA alleles, such as HLA‐DRB1 , have also been proven as a risk for developing RA.…”
Section: Introductionmentioning
confidence: 99%