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Published on: September 22, 2023
Feeding intolerance after pediatric cardiac surgery is associated with dysbiosis, barrier dysfunction, and reduced
Jacob Owens1, Haowen Qiu2, Cole Knoblich1
1Department of Pediatrics, University of Nebraska Medical Center, Omaha, Nebraska, United States.
Insights
Postoperative feeding intolerance in pediatric congenital heart disease is linked to gut microbiome changes, reduced beneficial short-chain fatty acids (SCFAs), and intestinal barrier dysfunction. Addressing these gut issues may improve patient outcomes after cardiac surgery.
Area of Science:
- Gastroenterology
- Pediatric Cardiology
- Microbiome Research
Background:
- Congenital heart disease (CHD) affects ~40,000 US infants annually, with 30-42% experiencing malnutrition and feeding intolerance (FI).
- Cardiopulmonary bypass (CPB) surgery for CHD can trigger inflammation, gut dysbiosis, and intestinal epithelial barrier dysfunction (EBD), potentially causing postoperative FI.
- FI in CHD patients is associated with prolonged hospitalization and increased mortality, highlighting the need to understand its underlying mechanisms.
Purpose of the Study:
- To investigate the relationship between postoperative FI and the intestinal microbiome, short-chain fatty acids (SCFAs), and EBD in pediatric CHD patients.
- To identify specific microbial shifts and metabolic changes associated with FI following cardiac surgery with CPB.
Main Methods:
- Prospective study of 26 pediatric patients (0-15 years) undergoing cardiac surgery with CPB.
- Collection of preoperative and postoperative samples for gut microbiome analysis, plasma EBD markers, SCFAs, and cytokines.
- Clinical data collection to calculate FI scores and assess patient status.
Main Results:
- Patients who developed FI (n=13) exhibited distinct microbial shifts, notably reduced SCFA-producing bacteria like Rothia and Clostridium innocuum.
- FI was associated with elevated plasma markers of EBD, including claudin-2, claudin-3, and fatty acid-binding protein.
- Patients with FI showed decreased plasma and stool SCFA levels, with mediation analysis linking microbiome changes to reduced butyric and propionic acid.
Conclusions:
- Novel evidence suggests intestinal dysbiosis, EBD markers, and SCFA depletion are significantly associated with postoperative FI in pediatric CHD.
- These findings highlight the gut microbiome's role in post-cardiac surgery outcomes and suggest potential therapeutic targets.
- Improving the intestinal milieu may enhance nutrition and clinical outcomes for pediatric patients undergoing cardiac surgery.
Abstract:
Congenital heart disease (CHD) is the most common birth defect, occurring in roughly 40,000 U.S. births annually. Malnutrition and feeding intolerance (FI) in CHD range from 30% to 42% and are associated with longer hospitalization and increased mortality. Cardiopulmonary bypass (CPB) required for surgical repair of CHD induces a systemic inflammatory response worsening intestinal dysbiosis and leading to intestinal epithelial barrier dysfunction (EBD), possibly contributing to postoperative FI. The objective of this study was to determine the relationship of postoperative FI with intestinal microbiome, short-chain fatty acids (SCFAs), and EBD in pediatric CHD after cardiac surgery. This was a prospective study of patients aged 0-15 years undergoing cardiac surgery with CPB. Samples were collected preoperatively and postoperatively to evaluate the gut microbiome, plasma EBD markers, short-chain fatty acids (SCFAs), and plasma cytokines. Clinical data were collected to calculate a FI score and evaluate patient status postoperatively. We enrolled 26 CPB patients and identified FI (n = 13). Patients with FI had unique microbial shifts with the reduced SCFA-producing organisms Rothia, Clostridium innocuum, and Intestinimonas. Patients who developed FI had associated elevations in the plasma EBD markers claudin-2 (P < 0.05), claudin-3 (P < 0.01), and fatty acid binding protein (P < 0.01). Patients with FI had reduced plasma and stool SCFAs. Mediation analysis showed the microbiome functional shift was associated with reductions in stool butyric and propionic acid in patients with FI. In conclusion, we provide novel evidence that intestinal dysbiosis, markers of EBD, and SCFA depletion are associated with FI. These data will help identify mechanisms and therapeutics to improve clinical outcomes following pediatric cardiac surgery.NEW & NOTEWORTHY Feeding intolerance contributes to postoperative morbidity following pediatric cardiac surgery. The intestinal microbiome and milieu play a vital role in gut function. Short-chain fatty acids are gut and cardioprotective metabolites produced by commensal bacteria and help maintain appropriate barrier function. Depletion of these metabolites and barrier dysfunction contribute to postoperative feeding intolerance following cardiac surgery. Identifying mechanistic targets to improve the intestinal milieu with the goal of improved nutrition and clinical outcomes is critical.
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