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NutriBrain: protocol for a randomised, double-blind, controlled trial to evaluate the effects of a nutritional product on brain integrity in preterm infants.
Hortensius, Lisa M; van den Hooven, Edith H; Dudink, Jeroen; Tataranno, Maria Luisa; van Elburg, Ruurd M; Benders, Manon J N L.
Afiliación
  • Hortensius LM; Department of Neonatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • van den Hooven EH; University Medical Center Utrecht Brain Center, Utrecht University, Utrecht, The Netherlands.
  • Dudink J; Danone Nutricia Research, Utrecht, The Netherlands.
  • Tataranno ML; Department of Neonatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • van Elburg RM; University Medical Center Utrecht Brain Center, Utrecht University, Utrecht, The Netherlands.
  • Benders MJNL; Department of Neonatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
BMC Pediatr ; 21(1): 132, 2021 03 17.
Article en En | MEDLINE | ID: mdl-33731062
ABSTRACT

BACKGROUND:

The gut microbiota and the brain are connected through different mechanisms. Bacterial colonisation of the gut plays a substantial role in normal brain development, providing opportunities for nutritional neuroprotective interventions that target the gut microbiome. Preterm infants are at risk for brain injury, especially white matter injury, mediated by inflammation and infection. Probiotics, prebiotics and L-glutamine are nutritional components that have individually already demonstrated beneficial effects in preterm infants, mostly by reducing infections or modulating the inflammatory response. The NutriBrain study aims to evaluate the benefits of a combination of probiotics, prebiotics and L-glutamine on white matter microstructure integrity (i.e., development of white matter tracts) at term equivalent age in very and extremely preterm born infants.

METHODS:

This study is a double-blind, randomised, controlled, parallel-group, single-center study. Eighty-eight infants born between 24 + 0 and < 30 + 0 weeks gestational age and less than 72 h old will be randomised after parental informed consent to receive either active study product or placebo. Active study product consists of a combination of Bifidobacterium breve M-16V, short-chain galacto-oligosaccharides, long-chain fructo-oligosaccharides and L-glutamine and will be given enterally in addition to regular infant feeding from 48 to 72 h after birth until 36 weeks postmenstrual age. The primary study outcome of white matter microstructure integrity will be measured as fractional anisotropy, assessed using magnetic resonance diffusion tensor imaging at term equivalent age and analysed using Tract-Based Spatial Statistics. Secondary outcomes are white matter injury, brain tissue volumes and cortical morphology, serious neonatal infections, serum inflammatory markers and neurodevelopmental outcome.

DISCUSSION:

This study will be the first to evaluate the effect of a combination of probiotics, prebiotics and L-glutamine on brain development in preterm infants. It may give new insights in the development and function of the gut microbiota and immune system in relation to brain development and provide a new, safe treatment possibility to improve brain development in the care for preterm infants. TRIAL REGISTRATION ISRCTN, ISRCTN96620855 . Date assigned 10/10/2017.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Probióticos / Bifidobacterium breve Tipo de estudio: Clinical_trials Límite: Humans / Infant / Newborn Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Probióticos / Bifidobacterium breve Tipo de estudio: Clinical_trials Límite: Humans / Infant / Newborn Idioma: En Año: 2021 Tipo del documento: Article