Associations between TNFSF4 and TRAF1-C5 gene polymorphisms and systemic lupus erythematosus: A meta-analysis

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Abstract

Objective: The aim of this study was to determine whether tumor necrosis factor superfamily 4 (TNFSF4) and TNF receptor-associated factor 1-complement 5 (TRAF1-C5) polymorphisms confer susceptibility to systemic lupus erythematosus (SLE). Methods: The authors conducted meta-analyses on associations between polymorphisms of the TNFSF4 (rs2205960, rs1234315, rs10489265) and TRAF1-C5 (rs10818488, rs3761847) genes and SLE susceptibility, using fixed and random effects models. Results: A total of 21 comparative studies were included in this meta-analysis; meta-analysis showed an association between the minor allele of rs2205960 of TNFSF4 and SLE in all study subjects (odds ratio [OR]=1.356, 95% confidence interval [CI]=1.275-1.442, p<1.0×10-9). Meta-analysis revealed an association between the minor alleles of rs1234315 and rs10489265 of TNFSF4 and SLE in Asians (OR=1.366, 95% CI=1.295-1.440, p<1.0×10-9; OR=1.463, 95% CI=1.208-1.771, p=9.7×10-5). The minor allele of rs10818488 of TRAF1-C5 was found to be significantly associated with SLE in Europeans (OR=1.210, 95% CI=1.115-1.313, p=5.0×10-6). The association p-values remained significant after multiple corrections. Conclusions: This meta-analysis confirms that TNFSF4 polymorphisms are associated with susceptibility to SLE in Asians and Europeans. An association was found between the rs10818488 polymorphism of TRAF1-C5 and susceptibility to SLE in Europeans.

Original languageEnglish
Pages (from-to)1050-1054
Number of pages5
JournalHuman Immunology
Volume73
Issue number10
DOIs
Publication statusPublished - 2012 Oct 1

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TNF Receptor-Associated Factor 1
Complement C5
Systemic Lupus Erythematosus
Meta-Analysis
Tumor Necrosis Factor-alpha
Genes
Odds Ratio
Confidence Intervals
Alleles

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

Cite this

Associations between TNFSF4 and TRAF1-C5 gene polymorphisms and systemic lupus erythematosus : A meta-analysis. / Lee, Young Ho; Song, Gwan Gyu.

In: Human Immunology, Vol. 73, No. 10, 01.10.2012, p. 1050-1054.

Research output: Contribution to journalArticle

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abstract = "Objective: The aim of this study was to determine whether tumor necrosis factor superfamily 4 (TNFSF4) and TNF receptor-associated factor 1-complement 5 (TRAF1-C5) polymorphisms confer susceptibility to systemic lupus erythematosus (SLE). Methods: The authors conducted meta-analyses on associations between polymorphisms of the TNFSF4 (rs2205960, rs1234315, rs10489265) and TRAF1-C5 (rs10818488, rs3761847) genes and SLE susceptibility, using fixed and random effects models. Results: A total of 21 comparative studies were included in this meta-analysis; meta-analysis showed an association between the minor allele of rs2205960 of TNFSF4 and SLE in all study subjects (odds ratio [OR]=1.356, 95{\%} confidence interval [CI]=1.275-1.442, p<1.0×10-9). Meta-analysis revealed an association between the minor alleles of rs1234315 and rs10489265 of TNFSF4 and SLE in Asians (OR=1.366, 95{\%} CI=1.295-1.440, p<1.0×10-9; OR=1.463, 95{\%} CI=1.208-1.771, p=9.7×10-5). The minor allele of rs10818488 of TRAF1-C5 was found to be significantly associated with SLE in Europeans (OR=1.210, 95{\%} CI=1.115-1.313, p=5.0×10-6). The association p-values remained significant after multiple corrections. Conclusions: This meta-analysis confirms that TNFSF4 polymorphisms are associated with susceptibility to SLE in Asians and Europeans. An association was found between the rs10818488 polymorphism of TRAF1-C5 and susceptibility to SLE in Europeans.",
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