The association of human milk intake and outcomes in biliary atresia.

Michael E Scheurer, Vicky Ng, Sarah A Taylor, John C Magee, Jeremy M Schraw, Sanjiv Harpavat, Benjamin L Shneider, Mary Elizabeth M Tessier, Stacey Beer, M Kyle Jensen

Journal: Journal of pediatric gastroenterology and nutrition 2025;80(1):163-173

PMID: 39526563

Abstract

OBJECTIVES

Human milk intake has many benefits which could influence outcomes in biliary atresia (BA). However, the role of human milk in BA has not been examined. We hypothesized that human milk intake would be associated with improved outcomes in BA.

METHODS

We assessed the impact of any human milk (AHM) as compared to formula only (FO) intake before Kasai portoenterostomy (KP) on outcomes in 447 infants with BA using the PROBE database (NCT00061828) post hoc. The primary outcome was clearance of jaundice (COJ = total bilirubin (TB) < 2 mg/dL by 3 months post-KP). Secondary outcomes included 2-year survival with native liver (SNL), bilirubin levels, cholangitis, ascites, and growth. We assessed the fecal microbiome (n = 8) comparing AHM versus FO.

RESULTS

At baseline, 211 infants received AHM and 215 received FO. 53.9% of AHM and 50.5% of FO achieved COJ (p = NS). SNL was insignificantly increased in AHM (odds ratio = 1.47, 95% confidence interval: 1.00-2.12, p = 0.053). TB decreased in AHM from 4 weeks to 3 months post-KP [4.8-4.0 mg/dL (p = 0.01)] unlike the FO group (4.9-4.9 mg/dL, p = 0.4). At 3 months post-KP, AHM infants had greater weight gain (1.88 ± 0.66 vs. 1.57 ± 0.73 kg, p < 0.001) and mid-upper arm circumference (12.9 ± 1.4 vs. 12.2 ± 1.7 cm, p < 0.001). Other secondary outcomes were not different. Microbiome differences were seen between AHM and FO.

CONCLUSIONS

Human milk intake in infants with BA did not significantly improve COJ or SNL. However, growth parameters were improved, and TB 3 months post-KP was decreased. Thus, human milk intake should not be discouraged. Prospective studies with detailed assessment of human milk intake are needed.

© 2024 European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.

Address: Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Section of Pediatric Gastroenterology Hepatology and Nutrition, Houston, Texas, USA.; Department of Pediatrics, Division of Hematology/Oncology, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.; Department of Pediatrics, Center for Epidemiology and Population Health, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.; Department of Pediatrics, Pediatric Gastroenterology, Hepatology and Nutrition, Primary Children's Hospital, University of Utah, Salt Lake City, Utah, USA.; Department of Surgery, University of Michigan Hospitals and Health Centers, Ann Arbor, Michigan, USA.; Division of Pediatric Gastroenterology, Hepatology and Nutrition, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Department of Pediatrics, Division of Gastroenterology Hepatology and Nutrition, Children's Hospital Colorado and University of Colorado School of Medicine, Aurora, Colorado, USA.
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