E26 Transformation- Specific-1 ( ETS1) and WDFY Family Member 4 ( WDFY4) Polymorphisms in Chinese Patients with Rheumatoid Arthritis

被引:16
|
作者
Zhang, Yiqun [1 ]
Bo, Lin [2 ]
Zhang, Hui [3 ]
Zhuang, Chao [3 ]
Liu, Ruiping [3 ,4 ]
机构
[1] Suzhou Univ, Affiliated Hosp, Dept Ophthalmol, Changzhou Peoples Hosp 4, Changzhou 213001, Jiangsu, Peoples R China
[2] Soochow Univ, Affiliated Hosp 2, Dept Rheumatol, Suzhou 215002, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp, Dept Orthoped, Changzhou Peoples Hosp 2, Changzhou 213003, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Affiliated Hosp, Cent Lab, Changzhou Peoples Hosp 2, Changzhou 213003, Jiangsu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
ETS1; WDFY4; polymorphisms; rheumatoid arthritis; molecular epidemiology; TRANSCRIPTION FACTOR; ASSOCIATION; EXPRESSION; CELLS; RISK;
D O I
10.3390/ijms15022712
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
E26 transformation-specific-1 (ETS1) and WDFY family member 4 (WDFY4) are closely related with systemic lupus erythematosus. We hypothesized that ETS1 and WDFY4 polymorphisms may contribute to rheumatoid arthritis (RA) susceptibility. We studied ETS1 rs1128334 G/A and WDFY4 rs7097397 A/G gene polymorphisms in 329 patients with RA and 697 controls in a Chinese population. Genotyping was done using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. When the WDFY4 rs7097397 AA homozygote genotype was used as the reference group, the AG genotype was associated with a significantly increased risk for RA. In the dominant model, when the WDFY4 rs7097397 AA homozygote genotype was used as the reference group, the AG/GG genotypes were associated with a significant increased susceptibility to RA. In stratification analyses, a significantly increased risk for RA associated with the WDFY4 rs7097397 AG genotype was evident among female patients, younger patients, C-reactive protein (CRP) negative patients and both anti-cyclic citrullinated peptide antibody (ACPA) positive patients and negative patients compared with the WDFY4 rs7097397 AA genotype. These findings suggested that WDFY4 rs7097397 A/G may be associated with the risk of RA, especially among younger, female patients, CRP-negative patients and both ACPA positive and negative patients. However, our results were obtained from a moderate-sized sample, and therefore this is a preliminary conclusion. To confirm these findings, validation by a larger study from a more diverse ethnic population is needed.
引用
收藏
页码:2712 / 2721
页数:10
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