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Updated: Sep 21, 2026

An Improved Method for the Preparation of Type I Collagen From Skin
Published on: January 21, 2014
Type 1 procollagen as a biochemical marker of growth in children with inflammatory bowel disease
Insights
Serum C-terminal propeptide of type I procollagen (pColl-I-C) levels reflect growth activity in children. This biomarker can assess therapeutic effects on growth in pediatric inflammatory bowel disease.
Area of Science:
- Biochemistry
- Pediatrics
- Gastroenterology
Background:
- Assessing growth in pediatric inflammatory bowel disease (IBD) is crucial.
- Type I collagen is a key component of bone and connective tissue.
- C-terminal propeptide of type I procollagen (pColl-I-C) is a marker of collagen synthesis.
Purpose of the Study:
- To measure serum pColl-I-C levels in children with functional bowel disease and IBD.
- To investigate the relationship between pColl-I-C, growth, and therapeutic interventions in pediatric IBD.
Main Methods:
- Radioimmunoassay was used to quantify serum pColl-I-C concentrations.
- Study included children with functional bowel disease, ulcerative colitis, and Crohn disease.
Main Results:
- Children with functional bowel disease and normal growth showed significantly higher pColl-I-C than adolescents.
- A significant relationship was observed between growth velocity and pColl-I-C in pediatric IBD patients.
- Daily prednisone therapy was associated with lower pColl-I-C levels compared to alternate-day or no prednisone therapy.
Conclusions:
- Serum pColl-I-C concentrations are indicative of growth activity in children.
- Repeated pColl-I-C measurements may offer a rapid method to evaluate the impact of therapies on growth in pediatric IBD.
Abstract:
Using radioimmunoassay, we measured the levels of the C-terminal propeptide of type I procollagen (pColl-I-C) in sera from 69 children with functional bowel disease (control population), 18 children with ulcerative colitis, and 35 children with Crohn disease. Sexually mature fully grown adolescents from all three patient groups had mean pColl-I-C concentrations (12.0 +/- 0.8 micrograms/dl) similar to those previously reported for adults (5 to 17 micrograms/dl). Children with functional bowel disease and normal growth had significantly higher concentrations (32.8 +/- 1.7 micrograms/dl) (P less than 0.001) than did the fully grown adolescents. In patients with inflammatory bowel disease a significant relationship between growth velocity and pColl-I-C concentrations was noted (P less than .001). Lower pColl-I-C concentrations were found in patients receiving daily prednisone therapy compared with those receiving alternate-day therapy (P less than 0.01) or those not taking the drug (P less than 0.01). These data suggest that pColl-I-C concentrations reflect growth activity in children. Repeated determinations may allow rapid assessment of the effects of various therapeutic modalities on growth in children with inflammatory bowel disease.
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