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Heritability of the limbic networks

Individual differences in cognitive ability and social behaviour are influenced by the variability in the structure and function of the limbic system. A strong heritability of the limbic cortex has been previously reported, but little is known about how genetic factors influence specific limbic netw...

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Autores principales: Budisavljevic, Sanja, Kawadler, Jamie M., Dell'Acqua, Flavio, Rijsdijk, Frühling V., Kane, Fergus, Picchioni, Marco, McGuire, Philip, Toulopoulou, Timothea, Georgiades, Anna, Kalidindi, Sridevi, Kravariti, Eugenia, Murray, Robin M., Murphy, Declan G., Craig, Michael C., Catani, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847695/
https://www.ncbi.nlm.nih.gov/pubmed/26714573
http://dx.doi.org/10.1093/scan/nsv156
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author Budisavljevic, Sanja
Kawadler, Jamie M.
Dell'Acqua, Flavio
Rijsdijk, Frühling V.
Kane, Fergus
Picchioni, Marco
McGuire, Philip
Toulopoulou, Timothea
Georgiades, Anna
Kalidindi, Sridevi
Kravariti, Eugenia
Murray, Robin M.
Murphy, Declan G.
Craig, Michael C.
Catani, Marco
author_facet Budisavljevic, Sanja
Kawadler, Jamie M.
Dell'Acqua, Flavio
Rijsdijk, Frühling V.
Kane, Fergus
Picchioni, Marco
McGuire, Philip
Toulopoulou, Timothea
Georgiades, Anna
Kalidindi, Sridevi
Kravariti, Eugenia
Murray, Robin M.
Murphy, Declan G.
Craig, Michael C.
Catani, Marco
author_sort Budisavljevic, Sanja
collection PubMed
description Individual differences in cognitive ability and social behaviour are influenced by the variability in the structure and function of the limbic system. A strong heritability of the limbic cortex has been previously reported, but little is known about how genetic factors influence specific limbic networks. We used diffusion tensor imaging tractography to investigate heritability of different limbic tracts in 52 monozygotic and 34 dizygotic healthy adult twins. We explored the connections that contribute to the activity of three distinct functional limbic networks, namely the dorsal cingulum (‘medial default-mode network’), the ventral cingulum and the fornix (‘hippocampal-diencephalic-retrosplenial network’) and the uncinate fasciculus (‘temporo-amygdala-orbitofrontal network’). Genetic and environmental variances were mapped for multiple tract-specific measures that reflect different aspects of the underlying anatomy. We report the highest heritability for the uncinate fasciculus, a tract that underpins emotion processing, semantic cognition, and social behaviour. High to moderate genetic and shared environmental effects were found for pathways important for social behaviour and memory, for example, fornix, dorsal and ventral cingulum. These findings indicate that within the limbic system inheritance of specific traits may rely on the anatomy of distinct networks and is higher for fronto-temporal pathways dedicated to complex social behaviour and emotional processing.
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spelling pubmed-48476952016-04-28 Heritability of the limbic networks Budisavljevic, Sanja Kawadler, Jamie M. Dell'Acqua, Flavio Rijsdijk, Frühling V. Kane, Fergus Picchioni, Marco McGuire, Philip Toulopoulou, Timothea Georgiades, Anna Kalidindi, Sridevi Kravariti, Eugenia Murray, Robin M. Murphy, Declan G. Craig, Michael C. Catani, Marco Soc Cogn Affect Neurosci Original Articles Individual differences in cognitive ability and social behaviour are influenced by the variability in the structure and function of the limbic system. A strong heritability of the limbic cortex has been previously reported, but little is known about how genetic factors influence specific limbic networks. We used diffusion tensor imaging tractography to investigate heritability of different limbic tracts in 52 monozygotic and 34 dizygotic healthy adult twins. We explored the connections that contribute to the activity of three distinct functional limbic networks, namely the dorsal cingulum (‘medial default-mode network’), the ventral cingulum and the fornix (‘hippocampal-diencephalic-retrosplenial network’) and the uncinate fasciculus (‘temporo-amygdala-orbitofrontal network’). Genetic and environmental variances were mapped for multiple tract-specific measures that reflect different aspects of the underlying anatomy. We report the highest heritability for the uncinate fasciculus, a tract that underpins emotion processing, semantic cognition, and social behaviour. High to moderate genetic and shared environmental effects were found for pathways important for social behaviour and memory, for example, fornix, dorsal and ventral cingulum. These findings indicate that within the limbic system inheritance of specific traits may rely on the anatomy of distinct networks and is higher for fronto-temporal pathways dedicated to complex social behaviour and emotional processing. Oxford University Press 2016-05 2015-12-28 /pmc/articles/PMC4847695/ /pubmed/26714573 http://dx.doi.org/10.1093/scan/nsv156 Text en © The Author (2015). Published by Oxford University Press. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Budisavljevic, Sanja
Kawadler, Jamie M.
Dell'Acqua, Flavio
Rijsdijk, Frühling V.
Kane, Fergus
Picchioni, Marco
McGuire, Philip
Toulopoulou, Timothea
Georgiades, Anna
Kalidindi, Sridevi
Kravariti, Eugenia
Murray, Robin M.
Murphy, Declan G.
Craig, Michael C.
Catani, Marco
Heritability of the limbic networks
title Heritability of the limbic networks
title_full Heritability of the limbic networks
title_fullStr Heritability of the limbic networks
title_full_unstemmed Heritability of the limbic networks
title_short Heritability of the limbic networks
title_sort heritability of the limbic networks
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847695/
https://www.ncbi.nlm.nih.gov/pubmed/26714573
http://dx.doi.org/10.1093/scan/nsv156
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