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Published in: Arthritis Research & Therapy 2/2014

Open Access 01-04-2014 | Research article

ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese

Authors: Shan Shan, Jie Dang, Jiangxia Li, Ze Yang, Hailing Zhao, Qian Xin, Xiaochun Ma, Yongchao Liu, Xianli Bian, Yaoqin Gong, Qiji Liu

Published in: Arthritis Research & Therapy | Issue 2/2014

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Abstract

Introduction

ETS1 is a negative regulator of the Th17 differentiation gene and plays a central role in the pathogenesis of autoimmune diseases. We aimed to investigate whether polymorphisms in ETS1 confer susceptibility to ankylosing spondylitis (AS) in Han Chinese.

Methods

We selected seven single nucleotide polymorphisms (SNPs) within ETS1 based on HapMap data and previous genome-wide association study. Genotyping involved the TaqMan method in 1,015 patients with AS and 1,132 healthy controls from Shandong Province, and 352 AS patients and 400 healthy controls from Ningxia, a northwest region in China. Gene expression was determined by real-time PCR.

Results

The SNP rs1128334 was strongly associated with AS (odds ratio 1.204, 95% confidence interval 1.06-1.37; P = 0.005). This association was confiexrmed in the Ningxia population (P = 0.015). Carriers of the haplotype TAT for rs12574073, rs1128334 and rs4937333 were associated with increased risk of AS and haplotype CGC with reduced risk as compared to controls. In addition, ETS1 expression was lower in AS patients than controls. The risk allele A of rs1128334 and haplotype A-T of rs1128334 and rs4937333 were associated with decreased expression of ETS1.

Conclusions

Common variants in ETS1 may contribute to AS susceptibility in Han Chinese people.
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Metadata
Title
ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese
Authors
Shan Shan
Jie Dang
Jiangxia Li
Ze Yang
Hailing Zhao
Qian Xin
Xiaochun Ma
Yongchao Liu
Xianli Bian
Yaoqin Gong
Qiji Liu
Publication date
01-04-2014
Publisher
BioMed Central
Published in
Arthritis Research & Therapy / Issue 2/2014
Electronic ISSN: 1478-6362
DOI
https://doi.org/10.1186/ar4530

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