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Therapeutic Methods and Therapies TCIM
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1.
Inflamm Bowel Dis ; 24(1): 101-110, 2017 12 19.
Article in English | MEDLINE | ID: mdl-29272494

ABSTRACT

Background: Individuals with Crohn's disease frequently require ileocecal resection (ICR), and inflammation often recurs in the neoterminal ileum following surgery. Fructooligosaccharide (FOS) is a fermentable prebiotic that stimulates the growth of bifidobacteria and may promote anti-inflammatory activity. The aim of this study was to determine if supplementation of a postICR diet with FOS in a mouse model would be effective in stimulating the growth of bifidobacteria and reducing systemic and local inflammation. Methods: ICR was performed in IL10-/- mice (129S1/SvlmJ) with colitis. Following surgery, nonICR control and ICR mice were fed a chow diet ± 10% FOS for 28 days. Serum, colon, and terminal ileum (TI) were analyzed for cytokine expression by MesoScale discovery platform. DNA extracted from stool was analyzed using 16s rRNA sequencing and qPCR. Expression of occludin and ZO1 was assessed using qPCR. Short-chain fatty acid (SCFA) concentrations were assessed using gas chromatography. Results: ICR led to increased systemic inflammation (P < 0.05) and a significant decline in fecal microbial diversity (P < 0.05). Mice on the FOS diet had a greater reduction in microbial diversity and also had worsened inflammation as evidenced by increased serum IL-6 (P < 0.05) and colonic IFNγ and TNFα (P < 0.05). Expression of occludin and ZO1 were significantly reduced in FOS-supplemented mice. There was a correlation between loss of diversity and the bifidogenic effectiveness of FOS (r = -0.61, P < 0.05). Conclusions: FOS-supplementation of a postICR diet resulted in a decrease in fecal bacterial diversity, reduction in barrier function, and increased gut inflammation.


Subject(s)
Colitis/surgery , Dietary Supplements , Feces/microbiology , Gastrointestinal Microbiome , Inflammation/drug therapy , Interleukin-10/physiology , Oligosaccharides/administration & dosage , Animals , Bifidobacterium/growth & development , Colectomy , Colitis/complications , Colitis/physiopathology , Ileum/surgery , Inflammation/microbiology , Inflammation/pathology , Mice , Mice, Inbred ICR , Mice, Knockout , Prebiotics/administration & dosage
2.
JPEN J Parenter Enteral Nutr ; 41(5): 866-877, 2017 07.
Article in English | MEDLINE | ID: mdl-26838529

ABSTRACT

BACKGROUND: To examine whether SMOFlipid prevents progression of intestinal failure-associated liver disease (IFALD) in parenteral nutrition (PN)-dependent infants with early IFALD (conjugated bilirubin 17-50 µmol/L, 1-3 mg/dL). STUDY DESIGN: Pilot multicenter blinded randomized controlled trial comparing SMOFlipid with Intralipid. Patients received the trial lipid for up to 12 weeks, unless they achieved full enteral tolerance sooner. The primary clinical outcome was the serum conjugated bilirubin. RESULTS: Twenty-four infants (mean age, 6 weeks) participated in the trial (13 Intralipid and 11 SMOFlipid). At the time of trial enrollment, patients in both groups were receiving 90% of their calories by PN. Mean duration on trial was 8 weeks and did not differ according to treatment ( P = .99). At trial conclusion, patients who received SMOFlipid had a lower conjugated bilirubin than those who received Intralipid (mean difference, -59 µmol/L; P = .03). Patients receiving SMOFlipid were also more likely to have a decrease in serum conjugated bilirubin to 0 µmol/L than those in the Intralipid group over the entire observation period (hazard ratio, 10.6; 95%; P = .03). The time to achievement of full enteral tolerance did not differ statistically (hazard ratio, 1.3; P = .59) between the groups. There was no significant difference in safety outcomes between the groups. CONCLUSIONS: Compared with Intralipid, SMOFlipid reduces the risk of progressive IFALD in children with intestinal failure. This trial was registered at clinicaltrials.gov as NCT00793195.


Subject(s)
Fat Emulsions, Intravenous/therapeutic use , Intestinal Diseases/therapy , Liver Diseases/therapy , Phospholipids/therapeutic use , Soybean Oil/therapeutic use , Bilirubin/blood , Emulsions/therapeutic use , Female , Humans , Infant , Infant, Newborn , Intestinal Diseases/complications , Intestinal Mucosa/metabolism , Intestines/drug effects , Liver Diseases/complications , Male , Parenteral Nutrition, Total , Pilot Projects , Treatment Outcome
3.
J Pediatr ; 164(3): 652-4, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24321533

ABSTRACT

Our clinical experience led us to reassess the effect of sole omega-3 lipid therapy on hemostasis. We compared thromboelastography platelet mapping in neonatal piglets given sole omega-3 lipid. We identified abnormalities in reaction time (P = .025) and the arachidonic acid pathway (P = .025). The potential for bleeding complications from parenteral omega-3 lipid emulsion therapy in high-risk infants with liver disease has been dismissed but, on the basis of this data, should be reconsidered.


Subject(s)
Fat Emulsions, Intravenous/adverse effects , Fish Oils/adverse effects , Hemorrhage/chemically induced , Parenteral Nutrition , Animals , Blood Transfusion , Catheterization, Central Venous/adverse effects , Disease Models, Animal , Emulsions/administration & dosage , Fat Emulsions, Intravenous/administration & dosage , Fish Oils/administration & dosage , Humans , Infant , Intestinal Diseases/complications , Intestinal Diseases/drug therapy , Liver Diseases/drug therapy , Liver Diseases/etiology , Male , Phospholipids/administration & dosage , Platelet Function Tests , Soybean Oil/administration & dosage , Swine , Thrombelastography , Triglycerides
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