Alterations of the intestinal barrier in patients with autism spectrum disorders and in their first-degree relatives

J Pediatr Gastroenterol Nutr. 2010 Oct;51(4):418-24. doi: 10.1097/MPG.0b013e3181dcc4a5.

Abstract

Objectives: Intestinal permeability (IPT) was investigated in patients with autism as well as in their first-degree relatives to investigate leaky gut hypothesis. Faecal calprotectin (FC) was also measured in patients with autism, either with or without gastrointestinal symptoms, and in their first-degree relatives.

Patients and methods: IPT results, assessed by means of the lactulose/mannitol test, were compared with adult and child controls and with FC values.

Results: A high percentage of abnormal IPT values were found among patients with autism (36.7%) and their relatives (21.2%) compared with normal subjects (4.8%). Patients with autism on a reported gluten-casein-free diet had significantly lower IPT values compared with those who were on an unrestricted diet and controls. Gastrointestinal symptoms were present in 46.7% of children with autism: constipation (45.5%), diarrhoea (34.1%), and others (alternating diarrhoea/constipation, abdominal pain, etc: 15.9%). FC was elevated in 24.4% of patients with autism and in 11.6% of their relatives; it was not, however, correlated with abnormal IPT values.

Conclusions: The results obtained support the leaky gut hypothesis and indicate that measuring IPT could help to identify a subgroup of patients with autism who could benefit from a gluten-free diet. The IPT alterations found in first-degree relatives suggest the presence of an intestinal (tight-junction linked) hereditary factor in the families of subjects with autism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Pain / epidemiology
  • Analysis of Variance
  • Child
  • Child Development Disorders, Pervasive / epidemiology*
  • Child Development Disorders, Pervasive / metabolism
  • Comorbidity
  • Constipation / epidemiology
  • Diarrhea / epidemiology
  • Enzyme-Linked Immunosorbent Assay
  • Family
  • Feces
  • Female
  • Humans
  • Inflammation / epidemiology
  • Intestinal Diseases / epidemiology*
  • Intestinal Diseases / metabolism
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / physiopathology*
  • Italy / epidemiology
  • Leukocyte L1 Antigen Complex / metabolism
  • Male
  • Permeability

Substances

  • Leukocyte L1 Antigen Complex