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Coeliac disease: current approach and future prospects.

机译:腹腔疾病:当前方法和未来前景。

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Public anxiety over gluten has fuelled widespread demand for gluten-free food, yet coeliac disease remains significantly underdiagnosed and some confusion remains regarding optimal diagnostic practices. Small bowel histology is the gold standard for diagnosis. High-quality commercial enzyme-linked immunosorbent assays for transglutaminase immunoglobulin A and deamidated gliadin immunoglobulin A and G are sensitive tools for screening, but almost 10% of coeliac disease is seronegative and serological testing is unreliable in the very young, in people already following a gluten-reduced diet, and those using immunosuppressive medications. HLA DQA and DQB genotyping to show that alleles encoding HLA DQ2 and DQ8 are absent virtually excludes coeliac disease. Confirming histological remission reduces the risks of later complications, such as osteoporosis and cancer. Monitoring remission by serology is unreliable. Because gluten is an exogenous antigen and the small intestine is readily accessible, the immunopathogenesis of coeliac disease is better understood than other strongly major histocompatibility complex class II-associated diseases, such as type 1 diabetes mellitus. Therapeutic targets have been identified and drugs are under development to supplement or even replace gluten-free diet. With greater awareness and non-dietary therapeutics, diagnosis and treatment of coeliac disease will be increasingly prominent in medical practice.
机译:公众对麸质的焦虑情绪刺激了人们对无麸质食品的广泛需求,然而,腹腔疾病的诊断仍显着不足,并且关于最佳诊断方法仍存在一些困惑。小肠组织学是诊断的金标准。对于转谷氨酰胺酶免疫球蛋白A和脱酰胺化的麦醇溶蛋白免疫球蛋白A和G的高质量商业化酶联免疫吸附测定是筛查的敏感工具,但几乎10%的乳糜泻是血清阴性的,在已经接受过抗病毒药物的人群中,血清学检测并不可靠。减少麸质的饮食,以及使用免疫抑制药物的饮食。 HLA DQA和DQB基因分型显示没有编码HLA DQ2和DQ8的等位基因实际上排除了乳糜泻。确认组织学缓解可降低后来发生并发症的风险,例如骨质疏松症和癌症。通过血清学监测缓解是不可靠的。因为面筋是一种外源性抗原,并且小肠容易接近,所以与其他与II型强相关性强的复杂疾病(例如1型糖尿病)相比,乳糜泻的免疫发病机制得到了更好的理解。已经确定了治疗目标,并且正在开发药物以补充甚至替代无麸质饮食。随着更高的认识和非饮食疗法,腹腔疾病的诊断和治疗将在医学实践中日益突出。

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