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Infants with cystic fibrosis have altered fecal functional capacities with potential clinical and metabolic consequences

15 Sept 2021

Abstract excerpt

BACKGROUND: Infants with cystic fibrosis (CF) suffer from gastrointestinal (GI) complications, including pancreatic insufficiency and intestinal inflammation, which have been associated with impaired nutrition and growth. Recent evidence identified altered fecal microbiota taxonomic compositions in infants with CF relative to healthy infants that were characterized by differences in the abundances of taxa...

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PMID: 34525965
DOI: 10.1186/s12866-021-02305-z

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