The SUS is pleased to announce the two award winners for the best presentation by a resident in the 2018 Academic Surgical Congress Plenary Sessions, where the Senior Author is a SUS member. The presentations were graded by members of the SUS Executive Council and the winners will represent the SUS at the European Society for Surgical Research (ESSR) and the Society of Academic & Research Surgery (SARS) Annual Meetings.
Award Winner: Andrew Yeh, MD
Institution: University of Pittsburgh, Department of Surgery
Senior Author: Michael Morowitz, MD
Abstract Title: Whole-Food Enteral Nutrition Prevents Gut Dysbiosis and Improves Outcomes in a Mouse Colitis Model
Meeting: Society of Academic & Research Surgery (SARS) Annual Meeting, January 7-8, 2019 in London
Dr. Andrew Yeh is a general surgery resident at the University of Pittsburgh. He is originally from Toronto, Canada. He completed his undergraduate degree in pharmacology at the University of Toronto. He completed his medical degree at the John A. Burns School of Medicine at the University of Hawai’i. His current research focus is on the gut microbiota as it relates to critical illness.
Nutrition and Metabolism Research Paper Sessions
2832646 – Whole-Food Enteral Nutrition but Not Standard Chemically-Defined Formulas Improves Outcomes and Prevents Gut Dysbiosis in a Murine DSS-Colitis Model.
Andrew Yeh, MD1,2; Eric Conners, BSc2; Brian Firek, MS 2; Matthew B. Rogers, PhD2; Richard Cheek, MD2; Michael J. Morowitz, MD2
1Surgery, University of Pittsburgh, Pittsburgh, PA; 2Division of Pediatric General and Thoracic Surgery, Children’s Hospital of Pittsburgh of UPMC, Pittsburgh, PA
Purpose: Critically ill patients that cannot eat are almost universally fed with chemically-defined enteral formulas containing added sugar, additives such as emulsifiers, and a low fiber content. Such diets have been shown to promote gut dysbiosis that may worsen gut and systemic inflammation. Whole-food enteral formulas that are composed of natural ingredients may mitigate these effects and contribute to improved clinical outcomes. We hypothesize that whole-food enteral formulas will restore a healthy gut microbiota and reduce inflammation in critically ill patients. To test this hypothesis, we used a murine model of chemically-induced colitis as a surrogate for the gut inflammation seen commonly during critical illness.
Methods: C57BL/6 mice (3 randomized groups of 16 mice) received either chemically-defined formulas Vital (V) or Pediasure (P; Abbott Nutrition), or plant-based whole-food formula Liquid Hope (LH; Functional Formularies) for 7 days. Diets were isocaloric and available ad libitum. All mice were then given 4% dextran sodium sulfate (DSS) water or control water for 4 days, during which time they continued their experimental diets. Weights and disease activity indices (DAI) were measured daily. Upon sacrifice, plasma IL-6, fecal lipocalin-2, and colon length were measured. Fecal samples were collected from each group at three defined time points. Bacterial 16S rRNA gene sequences in each sample were amplified, sequenced on the Illumina MiSeq, and analyzed with QIIME. Cecal contents were analyzed for metabolites using ultra-performance liquid chromatography coupled with tandem mass spectrometry.
Results: The volume of consumed formula was not different across groups. After DSS exposure, weight loss was more severe (p<0.01) and DAIs were higher (p<0.01) in mice fed V or P compared to LH (Figure). Increased IL-6 plasma levels (p<0.01), decreased colon length (p<0.01), and a trend towards elevated fecal lipocalin-2 were observed in mice fed V and P compared to LH indicating more severe inflammation. The gut microbiome of mice fed V and P demonstrated reduced species diversity and altered species composition compared to LH (p<0.05). Specifically, LH mice compared to V and P contained a lesser abundance of Enterobacteriaceae (p<0.05), a family containing many Gram-negative pathogens and associated with gut inflammation, and higher abundance of Clostridiales (p<0.05), an order containing many commensal bacteria associated with immune homeostasis. The cecal contents of mice fed LH compared to V and P contained a significantly higher concentration of several beneficial anti-inflammatory compounds produced or metabolized by the microbiota, including lithocholic acid, a secondary bile acid, and hydroxycinnamic acid, a plant-derived polyphenol (p<0.05).
Conclusions: Mice fed LH in this model of gut inflammation had superior outcomes compared to mice fed V and P. LH maintained a healthy gut microbiota and stimulated production of anti-inflammatory metabolites in the gut. Future work will establish which microbiome alterations and metabolites resulting from whole-food nutrition protect against dysregulated inflammation, and whether the use of these diets can improve outcomes in critically ill or chronically ill tube-fed patients.
Financial support received from: Functional Formularies provided Liquid Hope for this experiment at no cost.
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