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首页> 外文期刊>Rheumatology International >TNF promoter -308 GA and LTA 252 AG polymorphisms in Portuguese patients with systemic lupus erythematosus
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TNF promoter -308 GA and LTA 252 AG polymorphisms in Portuguese patients with systemic lupus erythematosus

机译:葡萄牙系统性红斑狼疮患者的TNF启动子-308 G> A和LTA 252 A> G多态性

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摘要

The polymorphism of the tumor necrosis factor (TNF) promoter gene at position -308 and that of the lymphotoxin alpha (LTA) gene at position 252 have been implicated as genetic risk factors for systemic lupus erythematosus (SLE) in some populations. In a nested case–control study, we investigated the possible association of these polymorphisms with susceptibility to SLE and with phenotypic disease features in Portuguese Caucasian patients. TNF-308 GA and LTA 252 AG polymorphisms were determined by restriction fragment length polymorphism analysis in a cohort of 115 SLE patients and 152 unrelated healthy controls, and the magnitude of the association between genotypes and SLE diagnosis was calculated. For SLE patients, we also tested the association between disease characteristics and genotypes. No significant differences in genotype or allele frequencies could be identified between SLE cases and controls. Lupus nephritis (OR = 2.84; 95%CI 1.14–7.03, P = 0.02) and the presence of anti-Sm antibodies (OR = 3.11; 95%CI 1.08–8.94; P = 0.03) were significantly more prevalent among lupus patients possessing the TNF-308 A allele. The occurrence of nephritis was also higher in LTA 252 G allele carriers (OR = 2.90; 95%CI 1.12–7.54; P = 0.02). Our results do not support a major role of either the TNF-308 GA or the LTA 252 AG polymorphisms as genetic risk factors for SLE. Nevertheless, these polymorphisms appear to associate with the risk of renal lupus and distinct immunological features.
机译:在某些人群中,肿瘤坏死因子(TNF)启动子基因在-308位和252位淋巴毒素α(LTA)基因的多态性被认为是系统性红斑狼疮(SLE)的遗传危险因素。在一项嵌套的病例对照研究中,我们调查了葡萄牙白人患者中这些多态性与SLE易感性和表型疾病特征之间的可能联系。通过限制性内切酶片段长度多态性分析,在115名SLE患者和152名非相关健康对照人群中确定TNF-308 G> A和LTA 252 A> G多态性,并计算了基因型与SLE诊断之间的关联程度。对于SLE患者,我们还测试了疾病特征与基因型之间的关联。在SLE病例和对照之间没有发现基因型或等位基因频率的显着差异。狼疮性肾炎(OR = 2.84; 95%CI 1.14–7.03,P = 0.02)和抗Sm抗体的存在(OR = 3.11; 95%CI 1.08–8.94; P = 0.03)在患有狼疮的狼疮患者中更为普遍TNF-308 A等位基因。 LTA 252 G等位基因携带者中肾炎的发生率也更高(OR = 2.90; 95%CI 1.12–7.54; P = 0.02)。我们的结果不支持TNF-308 G> A或LTA 252 A> G多态性作为SLE的遗传危险因素的主要作用。然而,这些多态性似乎与肾狼疮的风险和独特的免疫学特征有关。

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  • 来源
    《Rheumatology International》 |2012年第8期|p.2239-2244|共6页
  • 作者单位

    Rheumatology Research Unit, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal;

    Rheumatology Research Unit, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal;

    Rheumatology Research Unit, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal;

    Rheumatology Research Unit, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal;

    Rheumatology Research Unit, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal;

    Rheumatology and Bone Metabolic Diseases, Hospital Santa Maria, Lisbon, Portugal;

    Rheumatology, Hospital Garcia de Orta, Almada, Portugal;

    Rheumatology Research Unit, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Systemic lupus erythematosus; Genetics; -308 TNF Ggt; A; LTA 252 Agt; G; Nephritis;

    机译:系统性红斑狼疮;遗传学;-308 TNF G A;LTA 252 A G;肾炎;

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