The Role of Inflammation in the Endothelial Dysfunction in a Cohort of Pediatric Patients With Inflammatory Bowel Disease

J Pediatr Gastroenterol Nutr. 2019 Sep;69(3):330-335. doi: 10.1097/MPG.0000000000002374.

Abstract

Objectives: Chronic inflammation plays a central role in the etiology of endothelial damage. Endothelial dysfunction (ED) is the inability of the artery to dilate in response to an endothelial stimulus. We assessed the ED by measuring the reactive hyperaemia index (RHI) and the flow-mediated dilation (FMD) in a cohort of pediatric patients affected by inflammatory bowel disease (IBD) and comparing these parameters to a group of healthy controls (HC).

Methods: Forty-one patients were consecutive enrolled. ED was evaluated by both the plethysmographic RHI method and the measurement of the FMD of brachial artery after occlusion of the blood flow. Differences between patients and controls were assessed by the Mann-Whitney test. In each patient with IBD, the main inflammation markers were detected and correlated to RHI and FMD by a linear regression test.

Results: We enrolled 26 (59%) patients with IBD and 18 (41%) HC. When comparing FMD value at diagnosis it was significantly lower in IBD patients than in HC (P = 0.04). This result was confirmed at follow-up, when this difference became even more significant (P = 0.004). A significant indirect correlation was found between FMD and fecal calprotectin (r: 0.17; P = 0.04). No differences were found when comparing RHI.

Conclusions: Our results suggest that inflammation could lead to ED assessed by ultrasound FMD. These data were not confirmed by RHI; however, this could be due to the lack of a standardized pediatric cut-off. More studies are necessary to confirm our data.

MeSH terms

  • Adolescent
  • Biomarkers / blood
  • Blood Flow Velocity
  • Brachial Artery / physiopathology
  • Case-Control Studies
  • Child
  • Cohort Studies
  • Endothelium, Vascular
  • Female
  • Humans
  • Inflammation / physiopathology*
  • Inflammatory Bowel Diseases / physiopathology*
  • Leukocyte L1 Antigen Complex / blood
  • Male
  • Vasculitis / physiopathology*

Substances

  • Biomarkers
  • Leukocyte L1 Antigen Complex