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Clinical, serologic, and histologic features of gluten sensitivity in children.
Francavilla, Ruggiero; Cristofori, Fernanda; Castellaneta, Stefania; Polloni, Carlo; Albano, Veronica; Dellatte, Stefania; Indrio, Flavia; Cavallo, Luciano; Catassi, Carlo.
Afiliação
  • Francavilla R; Interdisciplinary Department of Medicine, Pediatric Section, University of Bari, Bari, Italy. Electronic address: rfrancavilla@gmail.com.
  • Cristofori F; Interdisciplinary Department of Medicine, Pediatric Section, University of Bari, Bari, Italy.
  • Castellaneta S; Department of Pediatrics, San Paolo Hospital, Bari, Italy.
  • Polloni C; Department of Pediatrics, Rovereto Hospital, Rovereto, Italy.
  • Albano V; Department of Pediatrics, Università Politecnica delle Marche, Ancona, Italy.
  • Dellatte S; Tandoi Group, Corato, Italy.
  • Indrio F; Interdisciplinary Department of Medicine, Pediatric Section, University of Bari, Bari, Italy.
  • Cavallo L; Interdisciplinary Department of Medicine, Pediatric Section, University of Bari, Bari, Italy.
  • Catassi C; Department of Pediatrics, Università Politecnica delle Marche, Ancona, Italy.
J Pediatr ; 164(3): 463-7.e1, 2014 Mar.
Article em En | MEDLINE | ID: mdl-24252792
ABSTRACT

OBJECTIVE:

To describe the clinical, serologic, and histologic characteristics of children with gluten sensitivity (GS). STUDY

DESIGN:

We studied 15 children (10 males and 5 females; mean age, 9.6 ± 3.9 years) with GS who were diagnosed based on a clear-cut relationship between wheat consumption and development of symptoms, after excluding celiac disease (CD) and wheat allergy, along with 15 children with active CD (5 males and 10 females; mean age, 9.1 ± 3.1 years) and 15 controls with a functional gastrointestinal disorder (6 males and 9 females; mean age, 8.6 ± 2.7 years). All children underwent CD panel testing (native antigliadin antibodies IgG and IgA, anti-tissue transglutaminase antibody IgA and IgG, and anti-endomysial antibody IgA), hematologic assessment (hemoglobin, iron, ferritin, aspartate aminotransferase, erythrocyte sedimentation rate), HLA typing, and small intestinal biopsy (on a voluntary basis in the children with GS).

RESULTS:

Abdominal pain was the most prevalent symptom in the children with GS (80%), followed by chronic diarrhea in (73%), tiredness (33%), bloating (26%), limb pain, vomiting, constipation, headache (20%), and failure to thrive (13%). Native antigliadin antibodies IgG was positive in 66% of the children with GS. No differences in nutritional, biochemical, or inflammatory markers were found between the children with GS and controls. HLA-DQ2 was found in 7 children with GS. Histology revealed normal to mildly inflamed mucosa (Marsh stage 0-1) in the children with GS.

CONCLUSION:

Our findings support the existence of GS in children across all ages with clinical, serologic, genetic, and histologic features similar to those of adults.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipersensibilidade Alimentar / Glutens Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Pediatr Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipersensibilidade Alimentar / Glutens Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Pediatr Ano de publicação: 2014 Tipo de documento: Article