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Published on: February 15, 2018
Digestive enzyme replacement relieves growth failure in preterm infants with poor exocrine pancreatic function: a
Annette Münch1,2, Christoph Bührer3, Ann Carolin Longardt1,4
1Department of Neonatology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Insights
Exogenous digestive enzyme replacement improved weight gain in preterm infants with exocrine pancreatic insufficiency. This intervention, using a liquid microbial enzyme formulation, addressed poor growth linked to low fecal pancreatic elastase-1 (FPE-1) activity.
Area of Science:
- Neonatology
- Pediatric Gastroenterology
- Nutritional Science
Background:
- Growth failure in preterm infants is often associated with poor exocrine pancreatic function.
- Traditional enzyme preparations are unsuitable for preterm infants due to gavage tube size limitations.
Purpose of the Study:
- To retrospectively assess the impact of exogenous digestive enzyme replacement on growth in preterm infants with confirmed exocrine pancreatic insufficiency.
- To evaluate the efficacy of a liquid microbial enzyme formulation in preterm infants experiencing growth failure.
Main Methods:
- Retrospective analysis of 33 preterm infants (<1250g birth weight) with low fecal pancreatic elastase-1 (FPE-1) (<200 μg/g).
- Comparison of weight gain and weight gain per kilocalorie during 14-day periods before and after enzyme replacement therapy.
- Enzyme replacement consisted of a liquid formulation containing lipase and protease (6000 U lipase and 240 U protease kg-1 d-1).
Main Results:
- Average daily weight gain significantly increased from 14.4 g kg-1 d-1 to 17.4 g kg-1 d-1 (P = 0.001).
- Weight gain per kilocalorie also showed a significant improvement, increasing from 0.08 g kcal-1 d-1 to 0.11 g kcal-1 d-1.
- The degree of growth improvement correlated with the severity of prior growth failure.
Conclusions:
- Exogenous digestive enzyme replacement, using a liquid microbial formulation, is associated with improved growth in preterm infants exhibiting signs of exocrine pancreatic insufficiency.
- This therapeutic approach offers a viable option for managing growth failure in this vulnerable population.
Abstract:
In orally fed preterm infants, poor weight gain may be linked to low fecal pancreatic elastase-1 (FPE-1) activity, indicative of exocrine pancreatic insufficiency. The objective of this study was the retrospective assessment of the effect of exogenous digestive enzyme replacement by gavage in preterm infants with growth failure and low FPE-1 (<200 μg/g). We analyzed weight gain relative to baseline and caloric intake during 14-day periods before and after institution of digestive enzyme replacement containing 6000 U lipase and 240 U protease kg-1 d-1. Among 46 of 132 preterm infants < 1250g birth weight surviving to at least 14 days in whom FPE-1 was determined, 38 infants had low FPE-1 (< 200 μg/g), and 33 infants received exogenous digestive enzyme replacement. Average daily weight gain significantly increased from 14.4 [range 2.6-22.4] g kg-1 d-1 to 17.4 [8.4-29.0] g kg-1 d-1 (P = 0.001), as did weight gain per kcal, from 0.08 [0.02-0.13] g kcal-1 d-1 to 0.11 [0.05-0.18] g kcal-1 d-1.Conclusion: In preterm infants with signs and symptoms of exocrine pancreatic insufficiency, exogenous digestive enzyme replacement is associated with improved growth. What is Known: • Very preterm infants on full enteral nutrition may display growth failure linked to transient poor exocrine pancreatic function. • Porcine pancreatic enzymes covered with an acid-resistant coating are too large to pass the internal diameter of most gavage tubes used in very preterm infants. What is New: • Administration of a liquid formulation of acid-resistant microbial digestive enzymes in preterm infants with growth failure and low fecal pancreatic elastase-1 values was associated with improved weight gain. • Response to exogenous digestive enzyme replacement was associated with the prior extent of growth failure.
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