PMID- 17243138 OWN - NLM STAT- MEDLINE DCOM- 20070822 LR - 20180913 IS - 1078-0998 (Print) IS - 1078-0998 (Linking) VI - 13 IP - 6 DP - 2007 Jun TI - Protein and energy metabolism response to the initial dose of infliximab in children with Crohn's disease. PG - 737-44 AB - BACKGROUND: Tumor necrosis factor-alpha (TNF-alpha) may contribute to the alterations in protein and energy metabolism present in children with Crohn's disease (CD), who frequently suffer from growth disturbance. We hypothesized that anti-TNF-alpha therapy would reduce protein losses, due to decreased proteolysis and increased protein synthesis, and that anti-TNF-alpha therapy would decrease resting energy expenditure. METHODS: Children with active CD underwent metabolic assessment immediately before and 2 weeks following initial infliximab infusion. Using the stable isotopes [d5] phenylalanine and [1-13C] leucine, 2 independent measures of protein metabolism were determined during fasting and in response to parenteral nutrition. Energy expenditure, determined by indirect calorimetry, was measured in fasting and parenterally fed states. RESULTS: Fifteen children completed the study. Following infliximab therapy, significant reductions in proteolysis (P < 0.05) were noted in the fasting state (8%-11%) and during parenteral nutrition infusion (10%-12%). Phenylalanine utilization for protein synthesis decreased significantly (8%-13%) following infliximab (P < 0.05). Protein balance was not significantly altered. No significant changes in energy expenditure were observed following infliximab in fasting or parenterally fed states. Supplementation with parenteral nutrition resulted in significantly decreased proteolysis (8%-21%; P < 0.05), increased protein synthesis (37%-45%; P < 0.01), and improved protein balance (P < 0.01) compared to the fasting state. CONCLUSIONS: Following the initial infliximab infusion in children with CD, proteolysis and protein synthesis were significantly reduced in the fasting and parenterally fed states. Supplementation with parenteral nutrition resulted in significant improvements in protein metabolism compared to the fasting state both before and after infliximab therapy. FAU - Steiner, Steven J AU - Steiner SJ AD - Division of Pediatric Gastroenterology/Hepatology/Nutrition, James Whitcomb Riley Hospital for Children, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA. ssteiner@iupui.edu FAU - Pfefferkorn, Marian D AU - Pfefferkorn MD FAU - Fitzgerald, Joseph F AU - Fitzgerald JF FAU - Denne, Scott C AU - Denne SC LA - eng GR - M01 RR000750/RR/NCRR NIH HHS/United States GR - R01 HD29153/HD/NICHD NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PL - England TA - Inflamm Bowel Dis JT - Inflammatory bowel diseases JID - 9508162 RN - 0 (Anti-Inflammatory Agents) RN - 0 (Antibodies, Monoclonal) RN - 0 (Carbon Isotopes) RN - 47E5O17Y3R (Phenylalanine) RN - B72HH48FLU (Infliximab) RN - GMW67QNF9C (Leucine) SB - IM MH - Adolescent MH - Anti-Inflammatory Agents/*administration & dosage MH - Antibodies, Monoclonal/*administration & dosage MH - Calorimetry, Indirect MH - Carbon Isotopes MH - Child MH - Crohn Disease/*blood/*drug therapy MH - Energy Metabolism/*drug effects MH - Fasting/blood MH - Female MH - Follow-Up Studies MH - Humans MH - Infliximab MH - Infusions, Intravenous MH - Leucine/*blood MH - Male MH - Phenylalanine/*blood MH - Prospective Studies MH - Treatment Outcome EDAT- 2007/01/24 09:00 MHDA- 2007/08/23 09:00 CRDT- 2007/01/24 09:00 PHST- 2007/01/24 09:00 [pubmed] PHST- 2007/08/23 09:00 [medline] PHST- 2007/01/24 09:00 [entrez] AID - 10.1002/ibd.20102 [doi] PST - ppublish SO - Inflamm Bowel Dis. 2007 Jun;13(6):737-44. doi: 10.1002/ibd.20102.