Relationship between severe obesity and gut inflammation in children: what's next?

Ital J Pediatr. 2010 Oct 1:36:66. doi: 10.1186/1824-7288-36-66.

Abstract

Background: Preliminary evidence suggests an association between obesity and gut inflammation.

Aims: To evaluate the frequency of glucose abnormalities and their correlation with systemic and intestinal inflammation in severely obese children.

Patients and methods: Thirty-four children (25 males; median age 10.8 ± 3.4 yrs) with severe obesity (BMI >95%) were screened for diabetes with oral glucose tolerance test (OGTT), systemic inflammation with C-reactive protein (CRP) and gut inflammation with rectal nitric oxide (NO) and faecal calprotectin.

Results: BMI ranged from 23 to 44 kg/m2, and BMI z-score between 2.08 e 4.93 (median 2.69 ± 0.53). Glucose abnormalities were documented in 71% of patients: type 2 diabetes in 29%, impaired fasting glucose (IFG) in 58%, and impaired glucose tolerance (IGT) in 37.5%. Thirty-one patients (91%) were hyperinsulinemic. CRP was increased in 73.5% with a correlation between BMI z-score and CRP (p 0.03). Faecal calprotectin was increased in 47% patients (mean 77 ± 68), and in 50% of children with abnormal glucose metabolism (mean 76 ± 68 μg/g), with a correlation with increasing BMI z-score. NO was pathological in 88%, and in 87.5% of glucose impairment (mean 6.8 ± 5 μM).

Conclusions: In this study, the prevalence of glucose abnormalities in obese children is higher than in other series; furthermore, a correlation is present between markers of systemic and intestinal inflammation and glucose abnormalities.

MeSH terms

  • Biomarkers / analysis
  • Blood Glucose / metabolism
  • Body Mass Index
  • C-Reactive Protein / metabolism
  • Child
  • Diabetes Mellitus, Type 2 / diagnosis
  • Feces / chemistry
  • Female
  • Glucose Tolerance Test
  • Humans
  • Hyperinsulinism / diagnosis
  • Inflammation / metabolism*
  • Leukocyte L1 Antigen Complex / metabolism
  • Male
  • Nitric Oxide / metabolism
  • Obesity / metabolism*
  • Rectum / metabolism

Substances

  • Biomarkers
  • Blood Glucose
  • Leukocyte L1 Antigen Complex
  • Nitric Oxide
  • C-Reactive Protein