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Sphingomyelin in Brain and Cognitive Development: Preliminary Data

Sphingomyelin (SM) supports brain myelination, a process closely associated with cognitive maturation. The presence of SM in breast milk suggests a role in infant nutrition; however, little is known about SM contribution to healthy cognitive development. We investigated the link between early life d...

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Autores principales: Schneider, Nora, Hauser, Jonas, Oliveira, Manuel, Cazaubon, Elise, Mottaz, Sara Colombo, O’Neill, Barry V., Steiner, Pascal, Deoni, Sean C. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709232/
https://www.ncbi.nlm.nih.gov/pubmed/31324675
http://dx.doi.org/10.1523/ENEURO.0421-18.2019
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author Schneider, Nora
Hauser, Jonas
Oliveira, Manuel
Cazaubon, Elise
Mottaz, Sara Colombo
O’Neill, Barry V.
Steiner, Pascal
Deoni, Sean C. L.
author_facet Schneider, Nora
Hauser, Jonas
Oliveira, Manuel
Cazaubon, Elise
Mottaz, Sara Colombo
O’Neill, Barry V.
Steiner, Pascal
Deoni, Sean C. L.
author_sort Schneider, Nora
collection PubMed
description Sphingomyelin (SM) supports brain myelination, a process closely associated with cognitive maturation. The presence of SM in breast milk suggests a role in infant nutrition; however, little is known about SM contribution to healthy cognitive development. We investigated the link between early life dietary SM, later cognitive development and myelination using an exploratory observational study of neurotypical children. SM levels were quantified in infant nutrition products fed in the first three months of life and associated with myelin content (brain MRI) as well as cognitive development (Mullen scales of early learning; MSEL). Higher levels of SM were significantly associated with higher rates of change in verbal development in the first two years of life (r = 0.65, p < 0.001), as well as, higher levels of myelin content at 12–24 months, delayed onset and/or more prolonged rates of myelination in different brain areas. Second, we explored mechanisms of action using in vitro models (Sprague Dawley rat pups). In vitro data showed SM treatment resulted in increased proliferation [p = 0.0133 and p = 0.0434 at 4 and 10 d in vitro (DIV)], maturation (p = 0.467 at 4 d DIV) and differentiation (p = 0.0123 and p = 0.0369 at 4 and 10 DIV) of oligodendrocyte precursor cells (OPCs), as well as increased axon myelination (p = 0.0005 at 32 DIV). These findings indicate an impact of dietary SM on cognitive development in healthy children, potentially modulated by oligodendrocytes and increased axon myelination. Future research should include randomized controlled trials to substantiate efficacy of SM for cognitive benefits together with preclinical studies examining SM bioavailability and brain uptake.
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spelling pubmed-67092322019-08-26 Sphingomyelin in Brain and Cognitive Development: Preliminary Data Schneider, Nora Hauser, Jonas Oliveira, Manuel Cazaubon, Elise Mottaz, Sara Colombo O’Neill, Barry V. Steiner, Pascal Deoni, Sean C. L. eNeuro New Research Sphingomyelin (SM) supports brain myelination, a process closely associated with cognitive maturation. The presence of SM in breast milk suggests a role in infant nutrition; however, little is known about SM contribution to healthy cognitive development. We investigated the link between early life dietary SM, later cognitive development and myelination using an exploratory observational study of neurotypical children. SM levels were quantified in infant nutrition products fed in the first three months of life and associated with myelin content (brain MRI) as well as cognitive development (Mullen scales of early learning; MSEL). Higher levels of SM were significantly associated with higher rates of change in verbal development in the first two years of life (r = 0.65, p < 0.001), as well as, higher levels of myelin content at 12–24 months, delayed onset and/or more prolonged rates of myelination in different brain areas. Second, we explored mechanisms of action using in vitro models (Sprague Dawley rat pups). In vitro data showed SM treatment resulted in increased proliferation [p = 0.0133 and p = 0.0434 at 4 and 10 d in vitro (DIV)], maturation (p = 0.467 at 4 d DIV) and differentiation (p = 0.0123 and p = 0.0369 at 4 and 10 DIV) of oligodendrocyte precursor cells (OPCs), as well as increased axon myelination (p = 0.0005 at 32 DIV). These findings indicate an impact of dietary SM on cognitive development in healthy children, potentially modulated by oligodendrocytes and increased axon myelination. Future research should include randomized controlled trials to substantiate efficacy of SM for cognitive benefits together with preclinical studies examining SM bioavailability and brain uptake. Society for Neuroscience 2019-08-05 /pmc/articles/PMC6709232/ /pubmed/31324675 http://dx.doi.org/10.1523/ENEURO.0421-18.2019 Text en Copyright © 2019 Schneider et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Schneider, Nora
Hauser, Jonas
Oliveira, Manuel
Cazaubon, Elise
Mottaz, Sara Colombo
O’Neill, Barry V.
Steiner, Pascal
Deoni, Sean C. L.
Sphingomyelin in Brain and Cognitive Development: Preliminary Data
title Sphingomyelin in Brain and Cognitive Development: Preliminary Data
title_full Sphingomyelin in Brain and Cognitive Development: Preliminary Data
title_fullStr Sphingomyelin in Brain and Cognitive Development: Preliminary Data
title_full_unstemmed Sphingomyelin in Brain and Cognitive Development: Preliminary Data
title_short Sphingomyelin in Brain and Cognitive Development: Preliminary Data
title_sort sphingomyelin in brain and cognitive development: preliminary data
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709232/
https://www.ncbi.nlm.nih.gov/pubmed/31324675
http://dx.doi.org/10.1523/ENEURO.0421-18.2019
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