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从遗传学角度看乳糜泻。

A genetic perspective on coeliac disease.

机构信息

Department of Genetics, University Medical Centre Groningen and University of Groningen, Groningen, The Netherlands.

出版信息

Trends Mol Med. 2010 Nov;16(11):537-50. doi: 10.1016/j.molmed.2010.09.003. Epub 2010 Oct 12.

Abstract

Coeliac disease is an inflammatory disorder of the small intestine with an autoimmune component and strong heritability. Genetic studies have confirmed strong association to HLA and identified 39 nonHLA risk genes, mostly immune-related. Over 50% of the disease-associated single nucleotide polymorphisms are correlated with gene expression. Most of the coeliac disease-associated regions are shared with other immune-related diseases, as well as with metabolic, haematological or neurological traits, or cancer. We review recent progress in the genetics of coeliac disease and describe the pathways these genes are in, the functional consequences of the associated markers on gene expression and the genes shared between coeliac disease and other traits.

摘要

乳糜泻是一种小肠的炎症性疾病,具有自身免疫成分和强烈的遗传性。遗传研究证实了与 HLA 的强烈关联,并确定了 39 个非 HLA 风险基因,主要与免疫有关。超过 50%的疾病相关的单核苷酸多态性与基因表达相关。乳糜泻相关的区域与其他免疫相关疾病以及代谢、血液学或神经特征或癌症共享。我们回顾了乳糜泻遗传学的最新进展,并描述了这些基因所在的途径、相关标记物对基因表达的功能后果以及乳糜泻和其他特征之间共享的基因。

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