乳糜泻的脱酰胺麦胶蛋白肽抗体:诊断驱动因素还是只是随波助澜?

Lerner Aaron, Haimi Motti, Matthias Torsten
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引用次数: 1

摘要

抗脱酰胺麦胶蛋白肽抗体被认为是乳糜泻相关的诊断抗体。近二十年来,它们一直在临床使用。在最初的十年中,它们优先用于儿童早期,面对IgA缺乏,偶尔推荐作为主要的血清学标记物,优于抗组织转谷氨酰胺酶自身抗体。值得注意的是,它们被推荐与组织转谷氨酰胺酶联合使用,作为诊断性能的增强剂。没有了,圆圈翻了过来。在第二个十年(2012-2019),大多数研究限制和批评了他们过去发表的优势。他们认为,在儿童早期、IgA缺乏、诊断性能以及两种抗体联合使用时,脱酰胺麦胶蛋白肽抗体与抗组织转谷氨酰胺酶自身抗体相比没有任何优势。看来,脱酰胺麦胶蛋白肽在乳糜泻算法诊断流程图中正在失去其地位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deamidated Gliadin Peptide Antibodies in Celiac Disease: A Diagnostic Driver or just along for the Ride?
Anti deamidated gliadin peptides antibodies are considered as celiac disease associated diagnostic antibodies. They are in clinical use for almost the last two decades. In the first decade they were preferentially used in early childhood, in face of IgA deficiency and occasionally recommended as the prime serological marker, outperforming the anti-tissue transglutaminase autoantibody. Notably, they were recommended in combination with the tissue transglutaminase as enhancer of the diagnostic performances. No more, the circle turned over. In the second decade (2012-2019), most of the studies limited and criticized their past published advantages. They suggested that deamidated gliadin peptides antibodies do not have any advantage over anti-tissue transglutaminase autoantibodies in terms of early childhood, IgA deficiency, diagnostic performances and when both antibodies are combined. It seems that the deamidated gliadin peptide are losing their place in the celiac disease algorithmic diagnostic flow chart.
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