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Erschienen in: Rheumatology International 5/2012

01.05.2012 | Original Article

A single-nucleotide polymorphism of the STAT4 gene is associated with systemic lupus erythematosus (SLE) in female Chinese population

verfasst von: Haixia Luan, Ping Li, Chunwei Cao, Chaohua Li, Chaojun Hu, Shulan Zhang, Xiaofeng Zeng, Fengchun Zhang, Changqing Zeng, Yongzhe Li

Erschienen in: Rheumatology International | Ausgabe 5/2012

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Abstract

Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease with complex genetic inheritance. Genetic association of signal transducer and activator of transcription 4 (STAT4) with SLE susceptibility has been convincingly established in multiple populations including Asians, whereas studies of genetic relations between STAT4 polymorphisms and subphenotypes of SLE were rarely conducted. In this study, we selected Chinese female population and investigated genetic association between a polymorphism of STAT4 gene (rs7582694) and SLE. Furthermore, genetic association tests based on different subsets classified by 11 clinical manifestations were also performed. A total of 675 SLE female patients and 678 healthy controls were enrolled into this study, and SNP genotyping was performed using Sequenom’s MassArray system (Sequenom iPLEX assay). Our study showed strong evidence for genetic predisposition of rs7582694 to SLE (X 2  = 23.7, OR = 0.68, 95% CI: 0.58–0.79, P = 1.13 × 10−6), while no association was observed between rs7582694 and any clinical presentations. The results of our study demonstrated that STAT4 rs7582694 SNP was significantly associated with SLE, and these results were in accordance with previous studies.
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Metadaten
Titel
A single-nucleotide polymorphism of the STAT4 gene is associated with systemic lupus erythematosus (SLE) in female Chinese population
verfasst von
Haixia Luan
Ping Li
Chunwei Cao
Chaohua Li
Chaojun Hu
Shulan Zhang
Xiaofeng Zeng
Fengchun Zhang
Changqing Zeng
Yongzhe Li
Publikationsdatum
01.05.2012
Verlag
Springer-Verlag
Erschienen in
Rheumatology International / Ausgabe 5/2012
Print ISSN: 0172-8172
Elektronische ISSN: 1437-160X
DOI
https://doi.org/10.1007/s00296-010-1767-9

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