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一种常见的CTLA4基因多态性使患有乳糜泻的儿童易患自身免疫性甲状腺疾病。

A common CTLA4 polymorphism confers susceptibility to autoimmune thyroid disease in celiac children.

作者信息

Tolone C, Cirillo G, Papparella A, Tolone S, Santoro N, Grandone A, Perrone L, del Giudice E Miraglia

机构信息

Department of Pediatrics F. Fede, Second University of Naples, Naples, Italy.

出版信息

Dig Liver Dis. 2009 Jun;41(6):385-9. doi: 10.1016/j.dld.2008.09.001. Epub 2008 Oct 16.

Abstract

BACKGROUND

Cytotoxic T-lymphocyte-associated protein 4 (CTLA4) is a strong candidate gene in autoimmunity susceptibility. In particular, the CTLA4 CT60 A/G dimorphism has been associated with celiac disease (CD) and was reported to be strongly associated with autoimmune thyroid disease (AITD).

AIMS

This study aimed to investigate the possible influences of the CTLA4 CT60 A/G polymorphism in the susceptibility of Italian children to CD and in the predisposition to develop AITD in children with CD.

PATIENTS AND METHODS

We genotyped 317 Italian celiac children, including 44 patients (13.9%) who developed AITD after CD diagnosis and 350 controls.

RESULTS

The CTLA4 CT60 GG genotype distribution did not show any significant difference between children with CD and control population (p=0.4). On the contrary, the frequency of the GG genotype was significantly higher in patients with CD complicated with AITD than in control subjects (p=0.002) and CD patients without AITD (p=0.02).

CONCLUSION

Our data show a significant effect of the CTLA4 CT60G allele at the homozygous state on the risk of developing AITD in children with CD and suggest that the reported association of the CTLA4 CT60 A/G polymorphism with CD is limited to the subgroup of patients who are or will be complicated with AITD.

摘要

背景

细胞毒性T淋巴细胞相关蛋白4(CTLA4)是自身免疫易感性的一个重要候选基因。特别是,CTLA4 CT60 A/G二态性与乳糜泻(CD)相关,并且据报道与自身免疫性甲状腺疾病(AITD)密切相关。

目的

本研究旨在调查CTLA4 CT60 A/G多态性对意大利儿童患CD易感性以及CD患儿发生AITD易感性的可能影响。

患者和方法

我们对317名意大利乳糜泻儿童进行了基因分型,其中包括44名(13.9%)在CD诊断后发生AITD的患者以及350名对照。

结果

CTLA4 CT60 GG基因型分布在CD患儿与对照人群之间未显示出任何显著差异(p = 0.4)。相反,CD合并AITD患者中GG基因型的频率显著高于对照受试者(p = 0.002)以及无AITD的CD患者(p = 0.02)。

结论

我们的数据表明,纯合状态的CTLA4 CT60G等位基因对CD患儿发生AITD的风险有显著影响,并提示所报道的CTLA4 CT60 A/G多态性与CD的关联仅限于已发生或将会发生AITD的患者亚组。

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