Fcγ receptor IIB and IIIB polymorphisms and susceptibility to systemic lupus erythematosus and lupus nephritis: A meta-analysis

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Abstract

The aim of this study was to explore whether polymorphisms of the Fcγ receptors (FcγRs) IIB T/I232 and FcγRIIIB NA1/NA2, confer susceptibility to systemic lupus erythematosus (SLE) and lupus nephritis (LN). The authors conducted a meta-analysis on associations between the FcγRIIB T/I232 and FcγRIIIB NA1/NA2 polymorphisms and SLE and LN susceptibility as determined using 1) allele contrast, 2) recessive, 3) dominant models and 4) contrast of homozygotes. A total of 16 separate comparisons were considered, consisting of 2887 SLE patients and 3105 controls. Meta-analysis of the FcγRIIB T/I232 polymorphism showed a significant association between the FcγRIIB T allele and the risk of developing SLE compared with the FcγRIIB I allele (OR = 1.207, 95% Cl = 1.061-1.373, P = 0.004). In subjects of Asian descent, a significant association was observed between the FcγRIIB T allele and SLE (OR = 1.332, 95% CI 1.138-1.558, P < 0.001). However, in Europeans no such association was found. In contrast, no association was found between SLE or LN and the FcγRIIIB NA1/NA2 polymorphism in all subjects, or in European and Asian populations. This meta-analysis shows that the FcγRIIB T/I232 polymorphism confers susceptibility to SLE, especially in Asian-derived populations.

Original languageEnglish
Pages (from-to)727-734
Number of pages8
JournalLupus
Volume18
Issue number8
DOIs
Publication statusPublished - 2009 Jun 18

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Lupus Nephritis
Fc Receptors
Systemic Lupus Erythematosus
Meta-Analysis
Alleles
Homozygote
Population

Keywords

  • Fc receptors
  • Genetic polymorphism
  • Meta-analysis
  • Systemic lupus erythematosus

ASJC Scopus subject areas

  • Rheumatology

Cite this

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title = "Fcγ receptor IIB and IIIB polymorphisms and susceptibility to systemic lupus erythematosus and lupus nephritis: A meta-analysis",
abstract = "The aim of this study was to explore whether polymorphisms of the Fcγ receptors (FcγRs) IIB T/I232 and FcγRIIIB NA1/NA2, confer susceptibility to systemic lupus erythematosus (SLE) and lupus nephritis (LN). The authors conducted a meta-analysis on associations between the FcγRIIB T/I232 and FcγRIIIB NA1/NA2 polymorphisms and SLE and LN susceptibility as determined using 1) allele contrast, 2) recessive, 3) dominant models and 4) contrast of homozygotes. A total of 16 separate comparisons were considered, consisting of 2887 SLE patients and 3105 controls. Meta-analysis of the FcγRIIB T/I232 polymorphism showed a significant association between the FcγRIIB T allele and the risk of developing SLE compared with the FcγRIIB I allele (OR = 1.207, 95{\%} Cl = 1.061-1.373, P = 0.004). In subjects of Asian descent, a significant association was observed between the FcγRIIB T allele and SLE (OR = 1.332, 95{\%} CI 1.138-1.558, P < 0.001). However, in Europeans no such association was found. In contrast, no association was found between SLE or LN and the FcγRIIIB NA1/NA2 polymorphism in all subjects, or in European and Asian populations. This meta-analysis shows that the FcγRIIB T/I232 polymorphism confers susceptibility to SLE, especially in Asian-derived populations.",
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T1 - Fcγ receptor IIB and IIIB polymorphisms and susceptibility to systemic lupus erythematosus and lupus nephritis

T2 - A meta-analysis

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AU - Ji, Jong Dae

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N2 - The aim of this study was to explore whether polymorphisms of the Fcγ receptors (FcγRs) IIB T/I232 and FcγRIIIB NA1/NA2, confer susceptibility to systemic lupus erythematosus (SLE) and lupus nephritis (LN). The authors conducted a meta-analysis on associations between the FcγRIIB T/I232 and FcγRIIIB NA1/NA2 polymorphisms and SLE and LN susceptibility as determined using 1) allele contrast, 2) recessive, 3) dominant models and 4) contrast of homozygotes. A total of 16 separate comparisons were considered, consisting of 2887 SLE patients and 3105 controls. Meta-analysis of the FcγRIIB T/I232 polymorphism showed a significant association between the FcγRIIB T allele and the risk of developing SLE compared with the FcγRIIB I allele (OR = 1.207, 95% Cl = 1.061-1.373, P = 0.004). In subjects of Asian descent, a significant association was observed between the FcγRIIB T allele and SLE (OR = 1.332, 95% CI 1.138-1.558, P < 0.001). However, in Europeans no such association was found. In contrast, no association was found between SLE or LN and the FcγRIIIB NA1/NA2 polymorphism in all subjects, or in European and Asian populations. This meta-analysis shows that the FcγRIIB T/I232 polymorphism confers susceptibility to SLE, especially in Asian-derived populations.

AB - The aim of this study was to explore whether polymorphisms of the Fcγ receptors (FcγRs) IIB T/I232 and FcγRIIIB NA1/NA2, confer susceptibility to systemic lupus erythematosus (SLE) and lupus nephritis (LN). The authors conducted a meta-analysis on associations between the FcγRIIB T/I232 and FcγRIIIB NA1/NA2 polymorphisms and SLE and LN susceptibility as determined using 1) allele contrast, 2) recessive, 3) dominant models and 4) contrast of homozygotes. A total of 16 separate comparisons were considered, consisting of 2887 SLE patients and 3105 controls. Meta-analysis of the FcγRIIB T/I232 polymorphism showed a significant association between the FcγRIIB T allele and the risk of developing SLE compared with the FcγRIIB I allele (OR = 1.207, 95% Cl = 1.061-1.373, P = 0.004). In subjects of Asian descent, a significant association was observed between the FcγRIIB T allele and SLE (OR = 1.332, 95% CI 1.138-1.558, P < 0.001). However, in Europeans no such association was found. In contrast, no association was found between SLE or LN and the FcγRIIIB NA1/NA2 polymorphism in all subjects, or in European and Asian populations. This meta-analysis shows that the FcγRIIB T/I232 polymorphism confers susceptibility to SLE, especially in Asian-derived populations.

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