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ArticleIndian journal of gastroenterology : official journal of the Indian Society of Gastroenterology2026

Role of intestinal fatty acid binding protein in the non-invasive diagnosis of celiac disease in children.

Sanjeevani Kaul, Rohan Malik, Tapish Pandey, Savita Saini, Alka Singh, Prasenjit Das, Govind Makharia

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Article in Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Sanjeevani KaulDivision of Pediatric Gastroenterology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Rohan MalikDivision of Pediatric Gastroenterology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110 029, India. dr.rohanmalik@gmail.com.ORCID http://orcid.org/0000-0003-3450-9668
Tapish PandeyDivision of Pediatric Gastroenterology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Savita SainiDivision of Pediatric Gastroenterology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Alka SinghDepartment of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Prasenjit DasDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Govind MakhariaDepartment of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, New Delhi, 110 029, India.

Funding

All-India Institute of Medical Sciences No.F.5-59/IRG/2010/RS
6 · The paper itself

Abstract

objectivesIntestinal fatty acid binding protein (IFABP) is a marker of intestinal epithelial injury and has been studied as a surrogate for predicting villous atrophy. The aim of this study was to evaluate the utility of IFABP in the non-invasive diagnosis of celiac disease (CeD) in children.

methodsSymptomatic children with positive anti-tissue transglutaminase antibody underwent a duodenal biopsy and IFABP measurement. Controls were included who had both tissue transglutaminase antibody (tTG) and IFABP measured. We evaluated the performance of IFABP in the diagnosis of CeD by generating the receiver operating characteristic (ROC) curve.

resultsTotal 123 children were screened; 98 had a positive anti-tTG, 74 patients aged 8.5 ± 4.0 years were diagnosed to have CeD and 24 patients had a normal biopsy. Seventy-six children aged 8.4 ± 4.0 years were enrolled as controls. Serum IFABP was significantly higher in children with CeD; median 918 pg/mL (interquartile range [IQR] = 630-1316) as compared to controls; median 386 pg/mL (IQR = 125-581) (p < 0.001). We observed increasing serum IFABP levels with a higher Marsh grade of mucosal injury (p < 0.001). Sensitivity and specificity for diagnosis of CD were 51% and 88% at serum IFABP level > 920 pg/mL and area under the curve (AUC) of 0.79 (0.67-0.90). In children with CD and a tTG 1-10 of normal, this cut-off could make a diagnosis without biopsy in 28/34 cases.

conclusionSerum IFABP can improve the non-invasive diagnosis of CeD in children with elevated tTG-IgA titers in a subset of patients and also has good correlation with the degree of villous atrophy.

Indexed as

Celiac DiseaseFatty Acid-Binding ProteinsAdolescentAutoantibodiesBiomarkersBiopsyChildChild, PreschoolDuodenumFemaleHumansIntestinal MucosaMaleROC CurveSensitivity and SpecificityTransglutaminasesAutoantibodiesBiomarkersFABP2 protein, humanFatty Acid-Binding ProteinsTransglutaminasesCeliac diseaseIntestinal fatty acid binding proteinNon-invasive diagnosisTissue transglutaminase antibody

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.