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1298A AASLD ABSTRACTS HEPATOLOGY, October, 2015<br />

2238<br />

Non-alcoholic fatty liver disease: assessment of intestinal<br />

microbiota and metabolites<br />

Hannah Da Silva 1,2 , Anastasia Teterina 1 , Bianca M. Arendt 1 ,<br />

Marialena Mouzaki 3 , Sandra E. Fischer 4 , Scott Fung 5 , Johane P.<br />

Allard 5 ; 1 Gastroenterology, Toronto General Hospital, Toronto,<br />

ON, Canada; 2 Department of Nutritional Sciences, University of<br />

Toronto, Toronto, ON, Canada; 3 GI/Hepatology/Nutrition, Hospital<br />

for Sick Children, Toronto, ON, Canada; 4 Pathology, University<br />

Health Network, Toronto, ON, Canada; 5 Medicine, Toronto<br />

General Hospital, Toronto, ON, Canada<br />

Background: Intestinal microbiota (IM) may contribute to non-alcoholic<br />

fatty liver disease (NAFLD) through products of bacterial<br />

metabolism. This study aimed to characterize the bacterial<br />

products present in serum and stool of NAFLD patients and<br />

HC and to examine the relationship between these products<br />

and IM. Methods: This was a prospective, cross-sectional<br />

study. Fecal and serum metabolite profiles of 39 patients with<br />

biopsy-proven NAFLD and 28 living liver donors as HC were<br />

examined using nuclear magnetic resonance spectroscopy.<br />

Metabolic profiles included 11 fecal and 9 serum bacterial<br />

products. In a subset of 29 NAFLD and 16 HC, IM composition<br />

was assessed. Clinical, biochemical, and anthropometric<br />

data were also collected. Quantitative real-time polymerase<br />

chain reaction was used to measure total bacterial counts,<br />

Firmicutes:Bacteroidetes ratio, Bacteroidetes, C. leptum, C.<br />

coccoides, Bifidobacteria, E. coli and Archaea in stool. Continuous<br />

variables were non-normal and described as median<br />

(Q1, Q3). Groups were compared using Wilcoxon rank-sum<br />

tests. Spearman correlation coefficients were used to examine<br />

association between IM and bacterial products. Results:<br />

NAFLD patients were older than HC with higher BMI, liver<br />

enzymes (AST, ALT), insulin resistance (HOMA-IR), hemoglobin<br />

A1c, and blood triglycerides (p

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