Cargando…

From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth

Very preterm (VPT) infants admitted to Neonatal Intensive Care Unit (NICU) are at risk for altered brain growth and less-than-optimal socio-emotional development. Recent research suggests that early NICU-related stress contributes to socio-emotional impairments in VPT infants at 3 months through epi...

Descripción completa

Detalles Bibliográficos
Autores principales: Fumagalli, Monica, Provenzi, Livio, De Carli, Pietro, Dessimone, Francesca, Sirgiovanni, Ida, Giorda, Roberto, Cinnante, Claudia, Squarcina, Letizia, Pozzoli, Uberto, Triulzi, Fabio, Brambilla, Paolo, Borgatti, Renato, Mosca, Fabio, Montirosso, Rosario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755830/
https://www.ncbi.nlm.nih.gov/pubmed/29304146
http://dx.doi.org/10.1371/journal.pone.0190602
_version_ 1783290641542807552
author Fumagalli, Monica
Provenzi, Livio
De Carli, Pietro
Dessimone, Francesca
Sirgiovanni, Ida
Giorda, Roberto
Cinnante, Claudia
Squarcina, Letizia
Pozzoli, Uberto
Triulzi, Fabio
Brambilla, Paolo
Borgatti, Renato
Mosca, Fabio
Montirosso, Rosario
author_facet Fumagalli, Monica
Provenzi, Livio
De Carli, Pietro
Dessimone, Francesca
Sirgiovanni, Ida
Giorda, Roberto
Cinnante, Claudia
Squarcina, Letizia
Pozzoli, Uberto
Triulzi, Fabio
Brambilla, Paolo
Borgatti, Renato
Mosca, Fabio
Montirosso, Rosario
author_sort Fumagalli, Monica
collection PubMed
description Very preterm (VPT) infants admitted to Neonatal Intensive Care Unit (NICU) are at risk for altered brain growth and less-than-optimal socio-emotional development. Recent research suggests that early NICU-related stress contributes to socio-emotional impairments in VPT infants at 3 months through epigenetic regulation (i.e., DNA methylation) of the serotonin transporter gene (SLC6A4). In the present longitudinal study we assessed: (a) the effects of NICU-related stress and SLC6A4 methylation variations from birth to discharge on brain development at term equivalent age (TEA); (b) the association between brain volume at TEA and socio-emotional development (i.e., Personal-Social scale of Griffith Mental Development Scales, GMDS) at 12 months corrected age (CA). Twenty-four infants had complete data at 12-month-age. SLC6A4 methylation was measured at a specific CpG previously associated with NICU-related stress and socio-emotional stress. Findings confirmed that higher NICU-related stress associated with greater increase of SLC6A4 methylation at NICU discharge. Moreover, higher SLC6A4 discharge methylation was associated with reduced anterior temporal lobe (ATL) volume at TEA, which in turn was significantly associated with less-than-optimal GMDS Personal-Social scale score at 12 months CA. The reduced ATL volume at TEA mediated the pathway linking stress-related increase in SLC6A4 methylation at NICU discharge and socio-emotional development at 12 months CA. These findings suggest that early adversity-related epigenetic changes might contribute to the long-lasting programming of socio-emotional development in VPT infants through epigenetic regulation and structural modifications of the developing brain.
format Online
Article
Text
id pubmed-5755830
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-57558302018-01-26 From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth Fumagalli, Monica Provenzi, Livio De Carli, Pietro Dessimone, Francesca Sirgiovanni, Ida Giorda, Roberto Cinnante, Claudia Squarcina, Letizia Pozzoli, Uberto Triulzi, Fabio Brambilla, Paolo Borgatti, Renato Mosca, Fabio Montirosso, Rosario PLoS One Research Article Very preterm (VPT) infants admitted to Neonatal Intensive Care Unit (NICU) are at risk for altered brain growth and less-than-optimal socio-emotional development. Recent research suggests that early NICU-related stress contributes to socio-emotional impairments in VPT infants at 3 months through epigenetic regulation (i.e., DNA methylation) of the serotonin transporter gene (SLC6A4). In the present longitudinal study we assessed: (a) the effects of NICU-related stress and SLC6A4 methylation variations from birth to discharge on brain development at term equivalent age (TEA); (b) the association between brain volume at TEA and socio-emotional development (i.e., Personal-Social scale of Griffith Mental Development Scales, GMDS) at 12 months corrected age (CA). Twenty-four infants had complete data at 12-month-age. SLC6A4 methylation was measured at a specific CpG previously associated with NICU-related stress and socio-emotional stress. Findings confirmed that higher NICU-related stress associated with greater increase of SLC6A4 methylation at NICU discharge. Moreover, higher SLC6A4 discharge methylation was associated with reduced anterior temporal lobe (ATL) volume at TEA, which in turn was significantly associated with less-than-optimal GMDS Personal-Social scale score at 12 months CA. The reduced ATL volume at TEA mediated the pathway linking stress-related increase in SLC6A4 methylation at NICU discharge and socio-emotional development at 12 months CA. These findings suggest that early adversity-related epigenetic changes might contribute to the long-lasting programming of socio-emotional development in VPT infants through epigenetic regulation and structural modifications of the developing brain. Public Library of Science 2018-01-05 /pmc/articles/PMC5755830/ /pubmed/29304146 http://dx.doi.org/10.1371/journal.pone.0190602 Text en © 2018 Fumagalli et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fumagalli, Monica
Provenzi, Livio
De Carli, Pietro
Dessimone, Francesca
Sirgiovanni, Ida
Giorda, Roberto
Cinnante, Claudia
Squarcina, Letizia
Pozzoli, Uberto
Triulzi, Fabio
Brambilla, Paolo
Borgatti, Renato
Mosca, Fabio
Montirosso, Rosario
From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth
title From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth
title_full From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth
title_fullStr From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth
title_full_unstemmed From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth
title_short From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth
title_sort from early stress to 12-month development in very preterm infants: preliminary findings on epigenetic mechanisms and brain growth
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755830/
https://www.ncbi.nlm.nih.gov/pubmed/29304146
http://dx.doi.org/10.1371/journal.pone.0190602
work_keys_str_mv AT fumagallimonica fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT provenzilivio fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT decarlipietro fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT dessimonefrancesca fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT sirgiovanniida fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT giordaroberto fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT cinnanteclaudia fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT squarcinaletizia fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT pozzoliuberto fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT triulzifabio fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT brambillapaolo fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT borgattirenato fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT moscafabio fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth
AT montirossorosario fromearlystressto12monthdevelopmentinverypreterminfantspreliminaryfindingsonepigeneticmechanismsandbraingrowth