Understanding Celiac Disease From Genetics to the Future Diagnostic Strategies.

Clinical Medicine Insights. Gastroenterology Pub Date : 2017-07-07 eCollection Date: 2017-01-01 DOI:10.1177/1179552217712249
Carolina Salazar, Jennyfer M García-Cárdenas, César Paz-Y-Miño
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引用次数: 9

Abstract

Celiac disease (CD) is an autoimmune disorder characterized by the permanent inflammation of the small bowel, triggered by the ingestion of gluten. It is associated with a number of symptoms, the most common being gastrointestinal. The prevalence of this illness worldwide is 1%. One of the main problems of CD is its difficulty to be diagnosed due to the various presentations of the disease. Besides, in many cases, CD is asymptomatic. Celiac disease is a multifactorial disease, HLA-DQ2 and HLA-DQ8 haplotypes are predisposition factors. Nowadays, molecular markers are being studied as diagnostic tools. In this review, we explore CD from its basic concept, manifestations, types, current and future methods of diagnosis, and associated disorders. Before addressing the therapeutic approaches, we also provide a brief overview of CD genetics and treatment.

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从遗传学到未来诊断策略理解腹腔疾病。
乳糜泻(CD)是一种自身免疫性疾病,其特征是由摄入麸质引发的小肠永久性炎症。它与许多症状有关,最常见的是胃肠道症状。这种疾病在全世界的流行率为1%。CD的主要问题之一是由于疾病的各种表现而难以诊断。此外,在许多情况下,CD是无症状的。腹腔疾病是一种多因素疾病,HLA-DQ2和HLA-DQ8单倍型是诱发因素。如今,分子标记物正被研究作为诊断工具。在这篇综述中,我们从CD的基本概念、表现、类型、当前和未来的诊断方法以及相关疾病等方面对其进行了探讨。在讨论治疗方法之前,我们还简要介绍了CD的遗传学和治疗。
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来源期刊
Clinical Medicine Insights. Gastroenterology
Clinical Medicine Insights. Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
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