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Celiac Disease in Children: A 2023 Update

Journal

INDIAN JOURNAL OF PEDIATRICS
Volume -, Issue -, Pages -

Publisher

SPRINGER INDIA
DOI: 10.1007/s12098-023-04659-w

Keywords

Celiac disease; Tissue transglutaminase; Anti-endomysial antibody; Gluten; Diarrhea

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Celiac disease is a chronic immune-mediated enteropathy caused by the ingestion of gluten in genetically predisposed individuals. It has a wide range of clinical manifestations and can affect people of all ages. The diagnosis is based on clinical history, serologic testing and duodenal biopsies. The management involves lifelong complete dietary avoidance of gluten, and monitoring of IgA-TGA for mucosal healing.
Celiac disease (CeD) is a chronic immune-mediated enteropathy, which occurs in genetically predisposed individuals by the ingestion of gluten proteins present in wheat, barley and rye. The global pooled prevalence of CeD is 0.7% and it has been reported from nations all around the globe and can affect individuals of any age. It has a wide clinical spectrum ranging from being asymptomatic to being symptomatic with severe manifestations. Though initial descriptions of CeD focused on the classical presentation with gastrointestinal manifestations, in recent years it has been found that more patients have non-classical manifestations such as anemia, osteoporosis, increased transaminases, failure to thrive or short stature. The definitive diagnosis of CeD is based on a combination of clinical history, serologic testing with/without examination of duodenal biopsies. The preferred initial serologic test regardless of age for the detection of CeD is the tissue transglutaminase (IgA anti-tTG). Children with a high tTG-IgA (>= 10 ULN) AND a positive anti-endomysial IgA antibody (EMA) can be diagnosed to have CeD without the need for duodenal biopsies. The rest should undergo biopsies with at least 4 biopsies from the distal duodenum and at least 1 from the bulb. A correctly orientated biopsy showing increased intraepithelial cells and a villous to crypt ratio of <2 is suggestive of CeD. The management of CeD is a lifelong complete dietary avoidance of gluten. IgA-TGA acts as a surrogate marker for healing of the small-bowel mucosa and should be performed every 6 mo until normalization and then every 12-24 mo thereafter.

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