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Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach

Objectives: To test whether genetic associations with behavioral outcomes after early childhood traumatic brain injury (TBI) are enriched for biologic pathways underpinning neurocognitive and behavioral networks. Design: Cross-sectional evaluation of the association of genetic factors with early (~...

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Autores principales: Kurowski, Brad G., Treble-Barna, Amery, Pilipenko, Valentina, Wade, Shari L., Yeates, Keith Owen, Taylor, H. Gerry, Martin, Lisa J., Jegga, Anil G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540783/
https://www.ncbi.nlm.nih.gov/pubmed/31191606
http://dx.doi.org/10.3389/fgene.2019.00481
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author Kurowski, Brad G.
Treble-Barna, Amery
Pilipenko, Valentina
Wade, Shari L.
Yeates, Keith Owen
Taylor, H. Gerry
Martin, Lisa J.
Jegga, Anil G.
author_facet Kurowski, Brad G.
Treble-Barna, Amery
Pilipenko, Valentina
Wade, Shari L.
Yeates, Keith Owen
Taylor, H. Gerry
Martin, Lisa J.
Jegga, Anil G.
author_sort Kurowski, Brad G.
collection PubMed
description Objectives: To test whether genetic associations with behavioral outcomes after early childhood traumatic brain injury (TBI) are enriched for biologic pathways underpinning neurocognitive and behavioral networks. Design: Cross-sectional evaluation of the association of genetic factors with early (~ 6 months) and long-term (~ 7 years) post-TBI behavioral outcomes. We combined systems biology and genetic association testing methodologies to identify biologic pathways associated with neurocognitive and behavior outcomes after TBI. We then evaluated whether genes/single nucleotide polymorphism (SNPs) associated with these biologic pathways were more likely to demonstrate a relationship (i.e., enrichment) with short and long-term behavioral outcomes after early childhood TBI compared to genes/SNPs not associated with these biologic pathways. Setting: Outpatient research setting. Participants:140 children, ages 3–6:11 years at time of injury, admitted for a TBI or orthopedic injury (OI). Interventions: Not Applicable. Main Outcome Measures: Child behavior checklist total problems T score. Results: Systems biology methodology identified neuronal systems and neurotransmitter signaling (Glutamate receptor, dopamine, serotonin, and calcium signaling), inflammatory response, cell death, immune systems, and brain development as important biologic pathways to neurocognitive and behavioral outcomes after TBI. At 6 months post injury, the group (TBI versus OI) by polymorphism interaction was significant when the aggregate signal from the highest ranked 40% of case gene associations was compared to the control set of genes. At ~ 7 years post injury, the selected polymorphisms had a significant main effect after controlling for injury type when the aggregate signal from the highest ranked 10% of the case genes were compared to the control set of genes Conclusions: Findings demonstrate the promise of applying a genomics approach, informed by systems biology, to understanding behavioral recovery after pediatric TBI. A mixture of biologic pathways and processes are associated with behavioral recovery, specifically genes associated with cell death, inflammatory response, neurotransmitter signaling, and brain development. These results provide insights into the complex biology of TBI recovery.
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spelling pubmed-65407832019-06-12 Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach Kurowski, Brad G. Treble-Barna, Amery Pilipenko, Valentina Wade, Shari L. Yeates, Keith Owen Taylor, H. Gerry Martin, Lisa J. Jegga, Anil G. Front Genet Genetics Objectives: To test whether genetic associations with behavioral outcomes after early childhood traumatic brain injury (TBI) are enriched for biologic pathways underpinning neurocognitive and behavioral networks. Design: Cross-sectional evaluation of the association of genetic factors with early (~ 6 months) and long-term (~ 7 years) post-TBI behavioral outcomes. We combined systems biology and genetic association testing methodologies to identify biologic pathways associated with neurocognitive and behavior outcomes after TBI. We then evaluated whether genes/single nucleotide polymorphism (SNPs) associated with these biologic pathways were more likely to demonstrate a relationship (i.e., enrichment) with short and long-term behavioral outcomes after early childhood TBI compared to genes/SNPs not associated with these biologic pathways. Setting: Outpatient research setting. Participants:140 children, ages 3–6:11 years at time of injury, admitted for a TBI or orthopedic injury (OI). Interventions: Not Applicable. Main Outcome Measures: Child behavior checklist total problems T score. Results: Systems biology methodology identified neuronal systems and neurotransmitter signaling (Glutamate receptor, dopamine, serotonin, and calcium signaling), inflammatory response, cell death, immune systems, and brain development as important biologic pathways to neurocognitive and behavioral outcomes after TBI. At 6 months post injury, the group (TBI versus OI) by polymorphism interaction was significant when the aggregate signal from the highest ranked 40% of case gene associations was compared to the control set of genes. At ~ 7 years post injury, the selected polymorphisms had a significant main effect after controlling for injury type when the aggregate signal from the highest ranked 10% of the case genes were compared to the control set of genes Conclusions: Findings demonstrate the promise of applying a genomics approach, informed by systems biology, to understanding behavioral recovery after pediatric TBI. A mixture of biologic pathways and processes are associated with behavioral recovery, specifically genes associated with cell death, inflammatory response, neurotransmitter signaling, and brain development. These results provide insights into the complex biology of TBI recovery. Frontiers Media S.A. 2019-05-22 /pmc/articles/PMC6540783/ /pubmed/31191606 http://dx.doi.org/10.3389/fgene.2019.00481 Text en Copyright © 2019 Kurowski, Treble-Barna, Pilipenko, Wade, Yeates, Taylor, Martin and Jegga. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Kurowski, Brad G.
Treble-Barna, Amery
Pilipenko, Valentina
Wade, Shari L.
Yeates, Keith Owen
Taylor, H. Gerry
Martin, Lisa J.
Jegga, Anil G.
Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach
title Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach
title_full Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach
title_fullStr Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach
title_full_unstemmed Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach
title_short Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach
title_sort genetic influences on behavioral outcomes after childhood tbi: a novel systems biology-informed approach
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540783/
https://www.ncbi.nlm.nih.gov/pubmed/31191606
http://dx.doi.org/10.3389/fgene.2019.00481
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