The combination of Ile225Thr polymorphism of Fcg receptor IIB gene and hypersensitiveness as risk factor for human systemic lupus erythematosus in chinese populations
<b>Background:</b> The aim of this study was to investigate the role of <i> FcgRIIB</i> gene in susceptibility to systemic lupus erythematosus (SLE) using family-based association study and to examine possible interaction between the <i> Ile225Thr </i> (rs1050501,...
Saved in:
Main Authors: | , , , , , , |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2007-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | <b>Background:</b> The aim of this study was to investigate the role of <i> FcgRIIB</i> gene in susceptibility to systemic lupus erythematosus (SLE) using family-based association study and to examine possible interaction between the <i> Ile225Thr </i> (rs1050501, exon 5) polymorphism of<i> Fcg</i> receptor IIB gene and hypersensitivity. <b> Objectives:</b> A total of 119 patients with SLE from 95 nuclear families, aged 14 to 78 years, according to the American College of Rheumatology (ACR) 1997 criteria were recruited. In addition, 316 family members of these patients were also genotyped. Seventy patients and their 70 normal siblings from 95 nuclear families were selected by the case-combined-control design. <b> Materials and Methods: </b> A family-based association study was used to explore the relationship between gene polymorphism and SLE. We studied a single-nucleotide polymorphisms (SNPs) encoding non-synonymous substitution in the <i> FcgRIIB</i> gene with respect to genetic susceptibility to SLE, the <i> FcgRIIB</i> gene were genotyped by restriction fragment length polymorphism (RFLP) method. The interaction of gene-environment was assessed by conditional logistic regression model. <b> Results: </b> Among 119 SLE patients, The frequencies of <i> FcgRIIB Ile225Ile, Ile225Thr</i> and <i> Thr</i> 225<i> Thr</i> genotypes were 8.1%, 61.3% and 30.6%. Univariate (single-marker) family-based association tests (FBATs) demonstrated that variant allele at SNP rs1050501, in exon 5 of <i> FcgRIIB</i> gene was significantly associated with genetic susceptibility to SLE in additive model (exon 5, Z=3.707, <i> P</i> =0.00020). Transmission/disequilibrium test (TDT) and sibship disequilibuium test (SDT) analysis showed an excess of the allele of <i> 225Thr </i> (<i> Ile225Thr</i> loci) from heterozygous parents to affected offspring (c<sup> 2</sup>=7.14,<i> P</i> =0.0105); Moreover, conditional logistic regression results showed that there was statistically significant multiplicative interaction of <i> FcgRa!B</i> gene and the Hypersensitiveness [c<sup> 2</sup>=5.013,<i> P</i> =0.024; OR=2.444, CI (1.126-5.309)]. <b> Conclusions:</b> Our findings provide strong evidence suggesting a <i> Ile225Thr</i> polymorphism might be the susceptibility factor of SLE; a possible gene-environment interaction between hypersensitiveness and <i> Ile225Thr</i> mutation in Chinese population. |
---|---|
Item Description: | 0019-5154 |