Franck Arnaud-Battandier
Nestlé
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Featured researches published by Franck Arnaud-Battandier.
Digestive Diseases and Sciences | 2005
Nadeem A. Afzal; Susan Davies; Morine Paintin; Franck Arnaud-Battandier; J A Walker-Smith; Simon Murch; Robert Heuschkel; John Fell
Data supporting a response to treatment with exclusive enteral nutrition in pediatric colonic Crohn’s disease are few. We examined clinical and biochemical responses of ileal, colonic, and ileocolonic Crohn’s disease and assessed the endoscopic and histological colonic mucosal response in the colonic and ileocolonic groups.We prospectively enrolled 65 children (age: 8–17 years) with acute intestinal Crohn’s disease (Pediatric Crohn’s Disease Activity Index [PCDAI] > 20). After ileocolonoscopy, gastroscopy, and a barium meal and follow-through, they were distributed into three groups (ileal, n = 12, ileocolonic, n = 39; and colonic, n = 14). All patients received exclusive polymeric feed as treatment, with a repeat endoscopy at completion of treatment. At enrollment the ileal group had significantly less severe disease (P = 0.05) compared to the colonic and ileocolonic groups. However, the colonic disease group showed the least fall in PCDAI scores at completion of treatment with enteral nutrition (P = 0.03), with the lowest remission rate (50%, vs 82.1% in the ileocolonic and 91.7% in the ileal group [χ2 test, P = 0.021]). Endoscopic and histologic colonic mucosal assessment showed a posttreatment improvement in the ileocolonic (P ≤ 0.01) but not in the colonic disease group (P = ns). Children with disease in the colon respond better to enteral nutrition if the ileum is also involved. This may be due to different underlying inflammatory mechanisms. Detailed pretreatment assessment in studies of Crohn’s disease according to disease distribution with appropriate individualized tailoring of treatment may be important in this regard.
Critical Care Medicine | 2009
Cécile Loï; Jean-Fabien Zazzo; Eric Delpierre; Claire Niddam; Nathalie Neveux; Eric Curis; Franck Arnaud-Battandier; Luc Cynober
Objective:Immune-enhancing diets (IEDs) rich in arginine (ARG) reduce morbi-mortality in trauma and surgical patients. Among the pharmaconutrients inducing these effects, ARG may be involved by generating active metabolites such as glutamine (GLN). However, the ability of an ARG-enriched diet to normalize GLN plasma levels in intensive care unit (ICU) patients has never been documented. To analyze plasma GLN and related amino acid (AA) kinetics in response to an ARG-enriched IED in ICU surgical patients. Design:This prospective, randomized, single-blind, comparative study was performed on 22 patients randomized to receive total enteral nutrition for 7 days with either an ARG-enriched IED or a standard formula (rendered isonitrogenous to the IED, S group, n = 11), providing 30 kcal/kg/day and 0.3 g N/kg/day. Measurements:Plasma AA concentrations were measured on day 5 after a 3-hour washout period (basal values = T0) and after 30, 60, 90, 120, 180, and 360 minutes of enteral nutrition. The primary end point was the variation in plasma GLN from T0 to T90. Results:Only the IED-fed patients showed an increase in plasma levels of GLN (differences [T90 − T0]: +40 ± 6 vs. −35 ± 18 &mgr;mol/L, mean ± sem, p < 0.05, two-way analysis of variance), ARG (+35 ± 5 vs.+1 ± 4 &mgr;mol/L, p < 0.05), ornithine (+23 ± 6 vs. −2 ± 2 &mgr;mol/L, p < 0.05), and proline (+36 ± 10 vs. −6 ± 11 &mgr;mol/L, p < 0.05). Conclusion:To our knowledge, this is the first reported pharmacokinetic study on an IED even though these products have been on the market for 20 years. Our main result is that administering an ARG-enriched IED causes a significant increase in plasma GLN probably from de novo GLN synthesis from ARG. This suggests that the ARG present in IED can serve to supply GLN to ICU patients, who are usually depleted in this conditionally essential AA during injury.
Acta Paediatrica | 2001
Ac Phylactos; In Fasoula; Franck Arnaud-Battandier; J A Walker-Smith; Jm Fell
Crohns disease is characterized by chronic inflammation of the gastrointestinal mucosa, which can be successfully treated with enteral nutrition. In this study, the activities of the antioxidant metalloenzymes copper/zinc‐superoxide dismutase (Cu/Zn‐SOD) and selenium‐glutathione peroxidase (Se‐GPx) were determined in erythrocyte lysates from children with Crohns disease. Both enzymes exhibited significantly lower activities relative to healthy control subjects: 1.55 ±0.33 vs 2.13 ±0.75 SOD Umg‐1 protein (p < 0.025) for Cu/Zn‐SOD, and 61.9 ±17.7 vs 93.6 ±28.7 mUmg‐1 protein (p<0.01) for Se‐GPx. Treatment of patients with a specific polymeric diet, CT3211, for a period of 8 wk did not significantly alter the activities of the enzymes. In contrast, clinically, enteral nutritional therapy induced a remission in 13/14 children, and a significant fall in both median serum C‐reactive protein and mean serum tumour necrosis factor‐a levels.
Nestle Nutrition workshop series. Clinical & performance programme | 1999
J.M.E. Fell; Morine Paintin; A. Donnet-Hughes; Franck Arnaud-Battandier; Thomas T. MacDonald; J.A. Walker-Smith
We have been able to show that CT3211 is an effective oral treatment in children with active Crohns disease. It was well tolerated, and there were minimal side effects. At the mucosal site of disease there was macroscopic and histological improvement, together with evidence of downregulation of the pro-inflammatory cytokines IL-1 beta, IL-8, and IFN-gamma.
Nutrition Clinique Et Metabolisme | 2000
Luc Cynober; Emmanuel Alix; Franck Arnaud-Battandier; Marc Bonnefoy; Patrice Brocker; Marie-Josephe Cals; Christine Cherbut; Claire Coplo; Monique Ferry; Anne Ghisolfi-Marque; Thierry Kravtchenko; B. Lesourd; Catherine Mignot; Philippe Patureau Mirand
Journal of Pediatric Gastroenterology and Nutrition | 1997
J Me Fell; A Hollis; P Kitching; Morine Paintin; Franck Arnaud-Battandier; Thomas T. MacDonald; J A Walker-Smith
Journal of Pediatric Gastroenterology and Nutrition | 1998
J Me Fell; A Hollis; Morine Paintin; Franck Arnaud-Battandier; Thomas T. MacDonald; J A Walker-Smith
Nutrition Clinique Et Metabolisme | 2001
Lo.ı̈c Simon; Nadine Gaconnet; Franck Arnaud-Battandier; Philippe Hartemann
Nutrition Clinique Et Metabolisme | 2001
Linda Simon; Nadine Gaconnet; Franck Arnaud-Battandier; Ph. Hartemann
Nutrition Clinique Et Metabolisme | 2001
Nadine Gaconnet; Franck Arnaud-Battandier; Philippe Hartemann