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血清肠脂肪酸结合蛋白在乳糜泻无创诊断中的应用

Serum intestinal fatty acid-binding protein in the noninvasive diagnosis of celiac disease.

作者信息

Oldenburger Irene B, Wolters Victorien M, Kardol-Hoefnagel Tineke, Houwen Roderick H J, Otten Henny G

机构信息

Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, Utrecht, The Netherlands.

Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

APMIS. 2018 Mar;126(3):186-190. doi: 10.1111/apm.12800. Epub 2018 Jan 31.

DOI:10.1111/apm.12800
PMID:29383769
Abstract

Current diagnostic guidelines for celiac disease (CD) in pediatric patients require a duodenal biopsy if the IgA anti-tissue transglutaminase (tTG) is below 10x the upper limit of normal (ULN). Additional markers may enable a noninvasive diagnosis in this group. Serum intestinal-fatty acid-binding protein (I-FABP), a marker for intestinal epithelial damage, could be useful in this respect. A total of 95 children with a clinical suspicion of CD and tTG 1-10x ULN were investigated. All had a duodenal biopsy and analysis of serum I-FABP. A control group of 161 children with familial short stature and normal tTG was included. I-FABP levels in the 71 patients with tTG 1-10x ULN and biopsy-proven CD (median 725 pg/mL) were not significantly different (p = 0.13) from the levels in the 24 patients with a tTG 1-10x ULN but a normal biopsy (median 497 pg/mL). However, when combining tTG and I-FABP levels, 11/24 patients could have been diagnosed noninvasively if tTG is ≥ 50 U/mL and I-FABP ≥880 pg/mL or in 12/19 patients if tTG is ≥ 60 U/mL and I-FABP ≥ 620 pg/mL. Therefore, addition of I-FABP to the diagnostic procedure of CD may provide a noninvasive diagnosis in patients with a tTG ≥ 50 U/mL.

摘要

目前,儿童乳糜泻(CD)的诊断指南要求,如果IgA抗组织转谷氨酰胺酶(tTG)低于正常上限(ULN)的10倍,则需进行十二指肠活检。其他标志物可能有助于对这组患者进行非侵入性诊断。血清肠脂肪酸结合蛋白(I-FABP)是一种肠道上皮损伤标志物,在这方面可能有用。对95名临床怀疑患有CD且tTG为1-10倍ULN的儿童进行了调查。所有患儿均进行了十二指肠活检并检测了血清I-FABP。纳入了161名家族性身材矮小且tTG正常的儿童作为对照组。71名tTG为1-10倍ULN且经活检证实为CD的患者(中位数为725 pg/mL)的I-FABP水平与24名tTG为1-10倍ULN但活检正常的患者(中位数为497 pg/mL)相比,差异无统计学意义(p = 0.13)。然而,当结合tTG和I-FABP水平时,如果tTG≥50 U/mL且I-FABP≥880 pg/mL,24名患者中有11名可通过非侵入性诊断;如果tTG≥60 U/mL且I-FABP≥620 pg/mL,19名患者中有12名可通过非侵入性诊断。因此,在CD的诊断过程中加入I-FABP可能为tTG≥50 U/mL的患者提供非侵入性诊断。

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