Intestinal inflammation and impact on growth in children with cystic fibrosis
Jasbir Dhaliwal1, Steven Leach, Tamarah Katz
1*Department of Pediatric Gastroenterology, Sydney Children's Hospital Randwick †Discipline of Pediatrics, School of Women's and Children's Health, Medicine, University of New South Wales ‡Department of Nutrition and Dietetics §Clinical Trials Centre ||Department of Pediatric Respiratory, Sydney Children's Hospital Randwick, Sydney, Australia ¶Department of Pediatrics, University of Otago, Christchurch, New Zealand.
Insights
Children with cystic fibrosis (CF) show unique intestinal inflammation, with elevated fecal calprotectin but normal S100A12 and osteoprotegerin. Higher calprotectin levels correlate with poor growth in CF patients.
Area of Science:
- Pediatric Gastroenterology
- Inflammatory Bowel Disease Research
- Cystic Fibrosis Research
Background:
- Intestinal inflammation is a common complication in cystic fibrosis (CF).
- Assessing intestinal inflammation markers can help understand its impact on CF patients' nutritional status.
Purpose of the Study:
- To evaluate and compare fecal markers of intestinal inflammation in children with CF.
- To determine if intestinal inflammation adversely affects the nutritional phenotype in CF.
Main Methods:
- Fecal samples were collected from children with CF, healthy controls (HCs), and Crohn disease (CD) patients.
- Markers analyzed included calprotectin, S100A12, and osteoprotegerin.
- Associations between inflammatory markers and clinical/nutritional indices were examined in CF subjects.
Main Results:
- Children with CF had higher fecal calprotectin than HCs, but lower than CD patients.
- Abnormal fecal calprotectin was prevalent in CF patients with pancreatic insufficiency.
- Fecal calprotectin inversely correlated with weight and height z-scores in CF patients.
Conclusions:
- Cystic fibrosis exhibits a distinct pattern of intestinal inflammation, characterized by elevated fecal calprotectin and normal S100A12/osteoprotegerin.
- The severity of intestinal inflammation, indicated by fecal calprotectin, is significantly linked to impaired growth in CF.
Objective:
The aim of the study was to evaluate and compare faecal markers of intestinal inflammation in children with cystic fibrosis (CF), and determine whether intestinal inflammation adversely affects the nutritional phenotype.
Methods:
Faecal samples for markers of intestinal inflammation, calprotectin, S100A12, and osteoprotegerin, were collected from children with CF, healthy controls (HCs), and Crohn disease (CD). Associations between inflammatory markers and clinical and nutritional indices were determined in subjects with CF.
Results:
Twenty-eight children with CF (mean [standard deviation (SD)] 8.4 [3.3] years old, 22 pancreatic insufficient [PI]), 47 HC, and 30 CD were recruited. Mean (SD) faecal calprotectin in CF (94.3 [100.6] mg/kg) was greater than HC (26.7 [15.4] mg/kg, P < 0.0001), but lower than CD (2133 [2781] mg/kg, P = 0.0003). Abnormal faecal calprotectin was found in subjects only with PI (17/22 (77%), P = 0.001). There was no difference in faecal mean (SD) S100A12 (0.8 [0.9] vs 1.5 [2.2] mg/kg, P = 0.14) and osteoprotegerin concentrations (72.7 [52.2] vs 62.5 [0.0] pg/mL, P = 0.2) between CF and HC. Patients with CD had significantly elevated S100A12 and osteoprotegerin compared with CF and HC. Faecal calprotectin inversely correlated with both weight (r = -0.5, P = 0.003) and height z scores (r = -0.6, P = 0.002) in CF.
Conclusions:
The pattern of intestinal inflammation in CF is unique and distinct from inflammatory bowel disease, with elevated faecal calprotectin but normal faecal S100A12 and osteoprotegerin concentrations. The severity of intestinal inflammation, based on faecal calprotectin, significantly correlates with poor growth.
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