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Biochemical markers in Celiac disease.

机译:腹腔疾病的生化标志物。

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摘要

Celiac Disease is a worldwide spread condition affecting 1:100-1:200 individuals. It is a permanent food intolerance to ingested gluten in genetically predisposed subjects. In this review we analyze the biochemical markers of the disease going from laboratory findings to histology passing through genetics. Gluten intolerance is a unique model of autoimmune disease in which we can recognize the main environmental factor (gluten) and the more complex genetic background. In additional way, serological markers for monitoring the disease and a safe and effective therapy (gluten free diet) are also available. In deed the environmental factor such as gluten intake is necessary to trigger the disease but genetics also matter. HLA genes are the most studied but in recent times also not HLA related genes are giving proof of additional relative risk to disease if present. From histological point of view intra epithelial cell infiltration by several lymphocyte subsets is becoming more and more important also for understanding pathogenesis of the disease.
机译:乳糜泻是一种全球性传播疾病,影响了1:100-1:200的个体。它是遗传易感人群中摄取麸质的永久性食物不耐受。在这篇综述中,我们分析了疾病的生化标志物,从实验室发现到通过遗传学的组织学。面筋不耐受是一种自身免疫性疾病的独特模型,在其中我们可以识别出主要的环境因素(面筋)和更复杂的遗传背景。另外,还提供用于监测疾病的血清学标志物和安全有效的疗法(无麸质饮食)。实际上,诸如麸质摄入等环境因素是引发该疾病所必需的,但遗传因素也很重要。 HLA基因是研究最多的基因,但最近也没有HLA相关基因提供证据证明存在额外的相对疾病风险。从组织学的角度来看,几种淋巴细胞亚群对上皮细胞的浸润对于理解疾病的发病机理也变得越来越重要。

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