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The genetic basis of inter-individual variation in recovery from traumatic brain injury

Traumatic brain injury (TBI) is one of the leading causes of death among young people, and is increasingly prevalent in the aging population. Survivors of TBI face a spectrum of outcomes from short-term non-incapacitating injuries to long-lasting serious and deteriorating sequelae. TBI is a highly c...

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Autores principales: Cortes, Daniel, Pera, Martin F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820607/
https://www.ncbi.nlm.nih.gov/pubmed/33479258
http://dx.doi.org/10.1038/s41536-020-00114-y
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author Cortes, Daniel
Pera, Martin F.
author_facet Cortes, Daniel
Pera, Martin F.
author_sort Cortes, Daniel
collection PubMed
description Traumatic brain injury (TBI) is one of the leading causes of death among young people, and is increasingly prevalent in the aging population. Survivors of TBI face a spectrum of outcomes from short-term non-incapacitating injuries to long-lasting serious and deteriorating sequelae. TBI is a highly complex condition to treat; many variables can account for the observed heterogeneity in patient outcome. The limited success of neuroprotection strategies in the clinic has led to a new emphasis on neurorestorative approaches. In TBI, it is well recognized clinically that patients with similar lesions, age, and health status often display differences in recovery of function after injury. Despite this heterogeneity of outcomes in TBI, restorative treatment has remained generic. There is now a new emphasis on developing a personalized medicine approach in TBI, and this will require an improved understanding of how genetics impacts on long-term outcomes. Studies in animal model systems indicate clearly that the genetic background plays a role in determining the extent of recovery following an insult. A candidate gene approach in human studies has led to the identification of factors that can influence recovery. Here we review studies of the genetic basis for individual differences in functional recovery in the CNS in animals and man. The application of in vitro modeling with human cells and organoid cultures, along with whole-organism studies, will help to identify genes and networks that account for individual variation in recovery from brain injury, and will point the way towards the development of new therapeutic approaches.
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spelling pubmed-78206072021-01-29 The genetic basis of inter-individual variation in recovery from traumatic brain injury Cortes, Daniel Pera, Martin F. NPJ Regen Med Review Article Traumatic brain injury (TBI) is one of the leading causes of death among young people, and is increasingly prevalent in the aging population. Survivors of TBI face a spectrum of outcomes from short-term non-incapacitating injuries to long-lasting serious and deteriorating sequelae. TBI is a highly complex condition to treat; many variables can account for the observed heterogeneity in patient outcome. The limited success of neuroprotection strategies in the clinic has led to a new emphasis on neurorestorative approaches. In TBI, it is well recognized clinically that patients with similar lesions, age, and health status often display differences in recovery of function after injury. Despite this heterogeneity of outcomes in TBI, restorative treatment has remained generic. There is now a new emphasis on developing a personalized medicine approach in TBI, and this will require an improved understanding of how genetics impacts on long-term outcomes. Studies in animal model systems indicate clearly that the genetic background plays a role in determining the extent of recovery following an insult. A candidate gene approach in human studies has led to the identification of factors that can influence recovery. Here we review studies of the genetic basis for individual differences in functional recovery in the CNS in animals and man. The application of in vitro modeling with human cells and organoid cultures, along with whole-organism studies, will help to identify genes and networks that account for individual variation in recovery from brain injury, and will point the way towards the development of new therapeutic approaches. Nature Publishing Group UK 2021-01-21 /pmc/articles/PMC7820607/ /pubmed/33479258 http://dx.doi.org/10.1038/s41536-020-00114-y Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review Article
Cortes, Daniel
Pera, Martin F.
The genetic basis of inter-individual variation in recovery from traumatic brain injury
title The genetic basis of inter-individual variation in recovery from traumatic brain injury
title_full The genetic basis of inter-individual variation in recovery from traumatic brain injury
title_fullStr The genetic basis of inter-individual variation in recovery from traumatic brain injury
title_full_unstemmed The genetic basis of inter-individual variation in recovery from traumatic brain injury
title_short The genetic basis of inter-individual variation in recovery from traumatic brain injury
title_sort genetic basis of inter-individual variation in recovery from traumatic brain injury
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820607/
https://www.ncbi.nlm.nih.gov/pubmed/33479258
http://dx.doi.org/10.1038/s41536-020-00114-y
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