Lack of association between interleukin-6 promoter polymorphism at position -174 and Henoch-Schönlein pur pura.

医学 基因型 过敏性紫癜 胃肠病学 限制性片段长度多态性 发起人 等位基因 免疫学 单核苷酸多态性 基因 白细胞介素 基因多态性 肾炎 多态性(计算机科学) 内科学 聚合酶链反应 血管炎 遗传学 基因表达 生物 疾病 细胞因子
作者
Mahsa M. Amoli,Javier Martı́n,José A. Miranda‐Filloy,Carlos García‐Porrúa,William Ollier,Miguel Á. González‐Gay
出处
期刊:PubMed 卷期号:25 (1 Suppl 44): S6-9 被引量:10
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To assess whether polymorphism of the interleukin (IL)-6 gene at the position -174 was implicated in the incidence of Henoch-Schönlein pur-pura (HSP). A further objective was to determine if any relationship existed with severe systemic complications of HSP, in particular with severe renal and gastrointestinal involvement.Unselected patients from Northwest Spain with primary cutaneous vasculitis classified as HSP according to proposed criteria were studied. All patients included in the present study were required to have had at least 2 year's follow-up. Patients and controls were genotyped for a single biallelic (G/C) nucleotide polymorphism in the promoter region at the position -174 of the IL-6 gene by a polymerase reaction chain-restriction fragment length polymorphism (PCR-RFLP) method.Forty-six Caucasian HSP patients and 124 healthy matched controls were studied. No allele or genotype differences between the whole group of HSP and controls were observed. This was also the case when HSP patients were stratified by the presence of gastrointestinal complications, nephritis, and permanent renal involvement (renal sequelae).The polymorphism in IL-6 gene promoter (-174 G/C) does not appear to be a genetic risk factor for HSP in Northwest Spain.

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