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终末期肾衰竭患者白细胞介素1受体拮抗剂与肿瘤坏死因子-α基因多态性

Interleukin 1 receptor antagonist and tumor necrosis factor-alpha gene polymorphism in patients with end-stage renal failure.

作者信息

Shu Kuo-Hsiung, Cheng Chi-Hung, Wu Ming-Ju, Chen Cheng-Hsu, Lee Wen-Chin

机构信息

Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.

出版信息

Ren Fail. 2005;27(1):53-7.

Abstract

End-stage-renal disease (ESRD) is a final result of various etiologies. Prognostic indicators leading to ESRD in chronic kidney diseases have been studied extensively, of which, genetic factors remain a subject of great concern. Interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-alpha) are potent proinflammatory cytokines that are involved in several chronic kidney diseases. Studies on cytokine gene polymorphism have revealed important information about the role of genetic factors in disease susceptibility and severity. Gene polymorphism of interleukin-1 receptor antagonist (IL-1ra) and TNF-alpha were determined in 297 ESRD patients and in 145 normal healthy controls. IL-1ra gene polymorphism was characterized as a variable number of tandem repeats of a 86 bp sequence within intron 2. Five alleles were identified and were designated as IL1RN1, IL1RN2, IL1RN3, IL1RN4, and IL1RN5, corresponding to 4,2,5,3, and 6 repeats, respectively. A polymorphism in the promoter region of the TNF-alpha gene was also studied. This polymorphism involved a guanidine to adenosine transition at position -308 and was designated as TNF1 (- 308 G) and TNF2 (-308 A). The genotypes and allele frequencies were compared between patients and control group. The distributions of genotypes of IL-1ra and TNF-alpha did not differ significantly between ESRD patients and normal controls. Analysis of allele frequencies revealed a trend toward an increase in IL1RN2 frequency (7.5% versus 3.8 %, p=0.064) and noncarriage of TNF2 in the patient group (7.2% versus 11.0%, p=0.076) when compared with the control group. When both alleles were considered together, the patient group had a significantly higher frequency of carriage of IL1RN2 in combination with noncarriage of TNF2 (p=0.0468). We conclude that carriage of IL-1RN2 and noncarriage of TNF2 allele appear to be poor prognostic factors in patients suffering from various chronic renal diseases that eventually enter end-stage renal failure.

摘要

终末期肾病(ESRD)是多种病因导致的最终结果。慢性肾脏病中导致ESRD的预后指标已得到广泛研究,其中遗传因素仍是备受关注的课题。白细胞介素-1(IL-1)和肿瘤坏死因子-α(TNF-α)是参与多种慢性肾脏病的强效促炎细胞因子。细胞因子基因多态性研究揭示了遗传因素在疾病易感性和严重程度方面作用的重要信息。对297例ESRD患者和145例正常健康对照者进行白细胞介素-1受体拮抗剂(IL-1ra)和TNF-α基因多态性检测。IL-1ra基因多态性表现为内含子2中一段86 bp序列的串联重复数目可变。鉴定出五个等位基因,分别命名为IL1RN1、IL1RN2、IL1RN3、IL1RN4和IL1RN5,分别对应4、2、5、3和6次重复。还研究了TNF-α基因启动子区域的多态性。该多态性涉及-308位的鸟嘌呤到腺嘌呤的转换,分别命名为TNF1(-308 G)和TNF2(-308 A)。比较患者组和对照组的基因型及等位基因频率。ESRD患者和正常对照者之间IL-1ra和TNF-α的基因型分布无显著差异。等位基因频率分析显示,与对照组相比,患者组中IL1RN2频率有增加趋势(7.5%对3.8%,p = 0.064),且TNF2无携带率较高(7.2%对11.0%,p = 0.076)。当同时考虑两个等位基因时,患者组中IL1RN2携带且TNF2无携带的频率显著更高(p = 0.0468)。我们得出结论,IL-1RN2携带和TNF2等位基因无携带似乎是最终进入终末期肾衰竭的各种慢性肾脏病患者的不良预后因素。

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