Suppr超能文献

[川崎病与肿瘤坏死因子α及白细胞介素-10基因启动子多态性的相关性]

[The correlation between Kawasaki disease and polymorphisms of Tumor necrosis factor alpha and interleukin-10 gene promoter].

作者信息

Yang Jun, Li Cheng-rong, Li Yong-bai, Li Ruo-xin, Sun Lai-bao, Huang Hui-jun, Wang Guo-bing

机构信息

Shenzhen Children's Hospital, Shenzhen 518026, China.

出版信息

Zhonghua Er Ke Za Zhi. 2003 Aug;41(8):598-602.

Abstract

OBJECTIVE

Kawasaki disease (KD) is an acute febrile vasculitic syndrome of unknown etiology that preferentially affects coronary artery. It has been suggested that proinflammatory cytokines like tumor necrosis factor alpha (TNF-alpha) and interleukin-10 (IL-10) are key players during acute KD. Recently, the polymorphisms relative to major transcriptional start site of TNF-alpha and IL-10 gene were shown to influence the level of TNF-alpha and IL-10 production in vitro. This study was aimed to investigate the genetic association of TNF-alpha and IL-10 promoter polymorphisms in juvenile patients of Han nationality with KD, and to investigate the possible associations with clinical manifestations of the disease.

METHODS

Four polymorphism sites of TNF-alpha and IL-10 gene promoter regions from 96 children with KD were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). One hundred and sixty age-matched normal children of the Han nationality were used as control. All patients accepted Doppler echocardiography examination in order to differentiate coronary artery lesions.

RESULTS

There was significant difference in allele frequencies of -308 (A/G) site of the TNF-alpha gene between children of the Han nationality and those of Japanese and Caucasian in America. There were significant differences in the allele frequencies of -1082 (G/A), -819 (C/T) and -592 (A/C) of IL-10 gene between children of the Han nationality and their British Counterparts (P < 0.01). There was no significant difference in allele frequencies of -308 (A/G) site of TNF-alpha gene between children with KD and normal controls. There was no significant difference in the haplotypes and the allele frequencies of the above three sites of IL-10 between the two groups. However, when clinical features were examined, the genotype frequency of TNF-alpha-308A was significantly higher in IVIG-resistant KD patients than that of TNF-alpha-308G genotype (67% vs 5%, chi(c)(2) = 90.48, P < 0.01). The genotype of TNF-alpha-308A was closely associated with IVIG-resistant KD (P < 0.01, relative risk 42.25, 95% confidence interval 15.81-112.88). The haplotype frequency of IL-10 -1082A/-819T/-592A was also higher in patients with coronary artery lesion (CAL) caused by KD than those of Non-ATA haplotype (52% vs 20%, chi(2) = 18.36, P < 0.01). The haplotypes of IL-10 -1082A/-819T/-592A was significantly associated with CAL caused by KD (P < 0.01, relative risk 4.26, 95% confidence interval 2.20-8.25).

CONCLUSION

The genotype of TNF-alpha-308A is one of the important factors that probably influence the therapeutic effect of KD. The haplotypes (-1082/-819/-592) of IL-10 gene promoter might be related to the pathogenesis of coronary artery complication of KD and -1082A/-819T/-592A haplotypes might be regarded as a genetic marker of risk factor for coronary artery lesion in KD.

摘要

目的

川崎病(KD)是一种病因不明的急性发热性血管炎综合征,主要累及冠状动脉。有研究表明,肿瘤坏死因子α(TNF-α)和白细胞介素-10(IL-10)等促炎细胞因子在急性KD发病过程中起关键作用。最近研究显示,TNF-α和IL-10基因主要转录起始位点的多态性可影响体外TNF-α和IL-10的产生水平。本研究旨在探讨汉族青少年KD患者中TNF-α和IL-10启动子多态性的遗传关联,并研究其与疾病临床表现的可能关系。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术,检测96例KD患儿TNF-α和IL-10基因启动子区的4个多态性位点。选取160例年龄匹配的汉族正常儿童作为对照。所有患者均接受多普勒超声心动图检查以鉴别冠状动脉病变。

结果

汉族儿童与日本及美国白种人儿童相比,TNF-α基因-308(A/G)位点的等位基因频率存在显著差异。汉族儿童与英国儿童相比,IL-10基因-1082(G/A)、-819(C/T)和-592(A/C)位点的等位基因频率存在显著差异(P<0.01)。KD患儿与正常对照儿童相比,TNF-α基因-308(A/G)位点的等位基因频率无显著差异。两组间IL-10上述3个位点的单倍型及等位基因频率无显著差异。然而,在分析临床特征时发现,静脉注射免疫球蛋白(IVIG)抵抗型KD患者中TNF-α-308A基因型频率显著高于TNF-α-308G基因型(67%比5%,χ²=90.48,P<0.01)。TNF-α-308A基因型与IVIG抵抗型KD密切相关(P<0.01,相对危险度42.25,95%可信区间15.81-112.88)。KD所致冠状动脉病变(CAL)患者中,IL-10 -1082A/-819T/-592A单倍型频率也高于非ATA单倍型(52%比20%,χ²=18.36,P<0.01)。IL-10 -1082A/-819T/-592A单倍型与KD所致CAL显著相关(P<0.01,相对危险度4.26,95%可信区间2.20-8.25)。

结论

TNF-α-308A基因型可能是影响KD治疗效果的重要因素之一。IL-10基因启动子的单倍型(-1082/-819/-592)可能与KD冠状动脉并发症的发病机制有关,-1082A/-819T/-592A单倍型可作为KD冠状动脉病变危险因素的遗传标志物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验