FOXP3 Gene Variants in Patients with Systemic Lupus Erythematosus: Association with Disease Susceptibility in Men and Relationship with Abortion in Women.

IF 1.1 4区 医学 Q4 IMMUNOLOGY
Paria Heydarinejad, Nasser Gholijani, Zahra Habibagahi, Mohammad Reza Malekmakan, Zahra Amirghofran
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Abstract

Background: FOXP3, an important transcription factor of regulatory T cells has shown a contribution to the development of various autoimmune diseases.

Objectives: To investigate the influence of FOXP3 polymorphisms (rs3761548 and rs2294021) on systemic lupus erythematosus (SLE) susceptibility and patients' characteristics.

Methods: Genotyping was performed on 265 patients with SLE and 404 healthy controls using PCR-RFLP. Patients' demographic, laboratory, and clinical information were all documented. The relationship between the SNPs and patients' characteristics was statistically analyzed.

Results: The frequency of C/- genotype in male patients was significantly higher than in the healthy male controls, whereas the frequency of A/- genotype was lower (OR=0.53; 95% CI=0.28-1.00, p=.05). Analysis of the correlation between these SNPs and the patients' characteristics showed a longer disease duration in the rs3761548 C/- carriers and a correlation with arthralgia in both SNPs. In the females, there was a significant association between CC haplotype and disease susceptibility (OR=0.6, CI=0.38-0.94, p=.027). A significant association of both SNPs with the history of abortion was also detected. The frequencies of the rs3761548 AA (p=.006) and the rs2294021 CC genotypes (p=.038) and AC/AC combination (p=.033) were higher in women who had an abortion. We found a correlation between the rs3761548 AC genotype and the decreased C4 level and cardiovascular involvement, and the rs2294021 CC genotype with ESR, neurological involvement, and photosensitivity.

Conclusions: FOXP3 rs3761548 C/- genotype association with disease susceptibility in male patients, an association of both SNPs with the abortion risk in female patients, and the correlation between these SNPs and several clinical features of the patients suggest their association with the disease development and pathology.

系统性红斑狼疮患者FOXP3基因变异:与男性疾病易感性的关系以及与女性流产的关系
背景:FOXP3是调节性T细胞的重要转录因子,在多种自身免疫性疾病的发生发展中起着重要作用。目的:探讨FOXP3基因多态性rs3761548和rs2294021对系统性红斑狼疮(SLE)易感性及患者特征的影响。方法:采用PCR-RFLP对265例SLE患者和404例健康对照进行基因分型。患者的人口统计、实验室和临床信息都被记录下来。统计分析snp与患者特征的关系。结果:男性患者C/-基因型频率显著高于健康男性对照组,A/-基因型频率显著低于健康男性对照组(OR=0.53;95% CI=0.28-1.00, p= 0.05)。对这些snp与患者特征的相关性分析显示,rs3761548 C/-携带者的病程较长,两种snp均与关节痛相关。在女性中,CC单倍型与疾病易感性之间存在显著相关性(OR=0.6, CI=0.38-0.94, p= 0.027)。这两个snp与流产史的显著关联也被发现。流产妇女rs3761548 AA基因型(p= 0.006)、rs2294021 CC基因型(p= 0.038)和AC/AC组合基因型(p= 0.033)的频率较高。我们发现rs3761548 AC基因型与C4水平降低和心血管受累相关,rs2294021 CC基因型与ESR、神经受累和光敏性相关。结论:FOXP3 rs3761548 C/-基因型在男性患者中与疾病易感性相关,在女性患者中这两个snp与流产风险相关,并且这两个snp与患者的一些临床特征之间存在相关性,提示其与疾病的发展和病理相关。
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来源期刊
Iranian Journal of Immunology
Iranian Journal of Immunology Medicine-Immunology and Allergy
CiteScore
1.60
自引率
0.00%
发文量
50
审稿时长
12 weeks
期刊介绍: The Iranian Journal of Immunology (I.J.I) is an internationally disseminated peer-reviewed publication and publishes a broad range of experimental and theoretical studies concerned with all aspects of immunology.
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