Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs

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Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs. / Rasmussen, Stine Ostenfeldt; Martin, Lena; Østergaard, Mette Viberg; Rudloff, Silvia; Li, Yanqi; Roggenbuck, Michael; Bering, Stine Brandt; Sangild, Per Torp.

I: American Journal of Physiology: Gastrointestinal and Liver Physiology, Bind 311, Nr. 3, 01.09.2016, s. G480-G491.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Rasmussen, SO, Martin, L, Østergaard, MV, Rudloff, S, Li, Y, Roggenbuck, M, Bering, SB & Sangild, PT 2016, 'Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs', American Journal of Physiology: Gastrointestinal and Liver Physiology, bind 311, nr. 3, s. G480-G491. https://doi.org/10.1152/ajpgi.00139.2016

APA

Rasmussen, S. O., Martin, L., Østergaard, M. V., Rudloff, S., Li, Y., Roggenbuck, M., Bering, S. B., & Sangild, P. T. (2016). Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs. American Journal of Physiology: Gastrointestinal and Liver Physiology, 311(3), G480-G491. https://doi.org/10.1152/ajpgi.00139.2016

Vancouver

Rasmussen SO, Martin L, Østergaard MV, Rudloff S, Li Y, Roggenbuck M o.a. Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs. American Journal of Physiology: Gastrointestinal and Liver Physiology. 2016 sep. 1;311(3):G480-G491. https://doi.org/10.1152/ajpgi.00139.2016

Author

Rasmussen, Stine Ostenfeldt ; Martin, Lena ; Østergaard, Mette Viberg ; Rudloff, Silvia ; Li, Yanqi ; Roggenbuck, Michael ; Bering, Stine Brandt ; Sangild, Per Torp. / Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs. I: American Journal of Physiology: Gastrointestinal and Liver Physiology. 2016 ; Bind 311, Nr. 3. s. G480-G491.

Bibtex

@article{e0a7b159dddd46cb8925bd398ad6eec5,
title = "Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs",
abstract = "Mother's own milk is the optimal first diet for preterm infants, but donor human milk (DM) or infant formula (IF) is used when supply is limited. We hypothesized that a gradual introduction of bovine colostrum (BC) or DM improves gut maturation, relative to IF during the first 11 days after preterm birth. Preterm pigs were fed gradually advancing doses of BC, DM, or IF (3–15 ml·kg−1·3 h−1, n = 14–18) before measurements of gut structure, function, microbiology, and immunology. The BC pigs showed higher body growth, intestinal hexose uptake, and transit time and reduced diarrhea and gut permeability, relative to DM and IF pigs (P < 0.05). Relative to IF pigs, BC pigs also had lower density of mucosa-associated bacteria and of some putative pathogens in colon, together with higher intestinal villi, mucosal mass, brush-border enzyme activities, colonic short chain fatty acid levels, and bacterial diversity and an altered expression of immune-related genes (higher TNFα, IL17; lower IL8, TLR2, TFF, MUC1, MUC2) (all P < 0.05). Values in DM pigs were intermediate. Severe necrotizing enterocolitis (NEC) was observed in >50% of IF pigs, while only subclinical intestinal lesions were evident from DM and BC pigs. BC, and to some degree DM, are superior to preterm IF in stimulating gut maturation and body growth, using a gradual advancement of enteral feeding volume over the first 11 days after preterm birth in piglets. Whether the same is true in preterm infants remains to be tested.",
keywords = "donor human milk, bovine colostrum, infant formula, necrotizing enterocolitis, nutrient fortification",
author = "Rasmussen, {Stine Ostenfeldt} and Lena Martin and {\O}stergaard, {Mette Viberg} and Silvia Rudloff and Yanqi Li and Michael Roggenbuck and Bering, {Stine Brandt} and Sangild, {Per Torp}",
year = "2016",
month = sep,
day = "1",
doi = "10.1152/ajpgi.00139.2016",
language = "English",
volume = "311",
pages = "G480--G491",
journal = "American Journal of Physiology: Gastrointestinal and Liver Physiology",
issn = "0193-1857",
publisher = "American Physiological Society",
number = "3",

}

RIS

TY - JOUR

T1 - Bovine colostrum improves neonatal growth, digestive function, and gut immunity relative to donor human milk and infant formula in preterm pigs

AU - Rasmussen, Stine Ostenfeldt

AU - Martin, Lena

AU - Østergaard, Mette Viberg

AU - Rudloff, Silvia

AU - Li, Yanqi

AU - Roggenbuck, Michael

AU - Bering, Stine Brandt

AU - Sangild, Per Torp

PY - 2016/9/1

Y1 - 2016/9/1

N2 - Mother's own milk is the optimal first diet for preterm infants, but donor human milk (DM) or infant formula (IF) is used when supply is limited. We hypothesized that a gradual introduction of bovine colostrum (BC) or DM improves gut maturation, relative to IF during the first 11 days after preterm birth. Preterm pigs were fed gradually advancing doses of BC, DM, or IF (3–15 ml·kg−1·3 h−1, n = 14–18) before measurements of gut structure, function, microbiology, and immunology. The BC pigs showed higher body growth, intestinal hexose uptake, and transit time and reduced diarrhea and gut permeability, relative to DM and IF pigs (P < 0.05). Relative to IF pigs, BC pigs also had lower density of mucosa-associated bacteria and of some putative pathogens in colon, together with higher intestinal villi, mucosal mass, brush-border enzyme activities, colonic short chain fatty acid levels, and bacterial diversity and an altered expression of immune-related genes (higher TNFα, IL17; lower IL8, TLR2, TFF, MUC1, MUC2) (all P < 0.05). Values in DM pigs were intermediate. Severe necrotizing enterocolitis (NEC) was observed in >50% of IF pigs, while only subclinical intestinal lesions were evident from DM and BC pigs. BC, and to some degree DM, are superior to preterm IF in stimulating gut maturation and body growth, using a gradual advancement of enteral feeding volume over the first 11 days after preterm birth in piglets. Whether the same is true in preterm infants remains to be tested.

AB - Mother's own milk is the optimal first diet for preterm infants, but donor human milk (DM) or infant formula (IF) is used when supply is limited. We hypothesized that a gradual introduction of bovine colostrum (BC) or DM improves gut maturation, relative to IF during the first 11 days after preterm birth. Preterm pigs were fed gradually advancing doses of BC, DM, or IF (3–15 ml·kg−1·3 h−1, n = 14–18) before measurements of gut structure, function, microbiology, and immunology. The BC pigs showed higher body growth, intestinal hexose uptake, and transit time and reduced diarrhea and gut permeability, relative to DM and IF pigs (P < 0.05). Relative to IF pigs, BC pigs also had lower density of mucosa-associated bacteria and of some putative pathogens in colon, together with higher intestinal villi, mucosal mass, brush-border enzyme activities, colonic short chain fatty acid levels, and bacterial diversity and an altered expression of immune-related genes (higher TNFα, IL17; lower IL8, TLR2, TFF, MUC1, MUC2) (all P < 0.05). Values in DM pigs were intermediate. Severe necrotizing enterocolitis (NEC) was observed in >50% of IF pigs, while only subclinical intestinal lesions were evident from DM and BC pigs. BC, and to some degree DM, are superior to preterm IF in stimulating gut maturation and body growth, using a gradual advancement of enteral feeding volume over the first 11 days after preterm birth in piglets. Whether the same is true in preterm infants remains to be tested.

KW - donor human milk

KW - bovine colostrum

KW - infant formula

KW - necrotizing enterocolitis

KW - nutrient fortification

U2 - 10.1152/ajpgi.00139.2016

DO - 10.1152/ajpgi.00139.2016

M3 - Journal article

C2 - 27445345

VL - 311

SP - G480-G491

JO - American Journal of Physiology: Gastrointestinal and Liver Physiology

JF - American Journal of Physiology: Gastrointestinal and Liver Physiology

SN - 0193-1857

IS - 3

ER -

ID: 171546311