Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder
ABSTRACT: Recent theories regarding the pathophysiology of bipolar disorder suggest contributions of both neurodevelopmental and neurodegenerative processes. While structural neuroimaging studies indicate disease-associated neuroanatomical alterations, the behavioural correlates of these alterations...
- Autores:
-
Scott C. Fears
Remmelt, Schür
Sjouwerman, Rachel
Service, Susan K
Araya, Carmen
Araya, Xinia
Bejarano, Julio
Knowles, Emma
Gomez-Makhinson, Juliana
López Tobón, María Cecilia
Aldana, Ileana
Teshiba, Terri M.
Abaryan, Zvart
Al-Sharif, Noor B.
Navarro, Linda
Tishler, Todd A.
Altshuler, Lori
Bartzokis, George
Escobar, Javier I.
Glahn, David C.
Thompson, Paul M.
Lopez-Jaramillo, Carlos
Macaya, Gabriel
Molina, Julio
Reus, Victor I.
Sabatti, Chiara
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2015
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/25834
- Acceso en línea:
- http://hdl.handle.net/10495/25834
- Palabra clave:
- Trastorno Bipolar
Bipolar Disorder
Genealogía y Heráldica
Genealogy and Heraldry
Temperamento
Temperament
Imagen por Resonancia Magnética
Magnetic Resonance Imaging
Fenotipos
Phenotype
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc/2.5/co/
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oai:bibliotecadigital.udea.edu.co:10495/25834 |
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UDEA2 |
network_name_str |
Repositorio UdeA |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder |
title |
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder |
spellingShingle |
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder Trastorno Bipolar Bipolar Disorder Genealogía y Heráldica Genealogy and Heraldry Temperamento Temperament Imagen por Resonancia Magnética Magnetic Resonance Imaging Fenotipos Phenotype |
title_short |
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder |
title_full |
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder |
title_fullStr |
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder |
title_full_unstemmed |
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder |
title_sort |
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder |
dc.creator.fl_str_mv |
Scott C. Fears Remmelt, Schür Sjouwerman, Rachel Service, Susan K Araya, Carmen Araya, Xinia Bejarano, Julio Knowles, Emma Gomez-Makhinson, Juliana López Tobón, María Cecilia Aldana, Ileana Teshiba, Terri M. Abaryan, Zvart Al-Sharif, Noor B. Navarro, Linda Tishler, Todd A. Altshuler, Lori Bartzokis, George Escobar, Javier I. Glahn, David C. Thompson, Paul M. Lopez-Jaramillo, Carlos Macaya, Gabriel Molina, Julio Reus, Victor I. Sabatti, Chiara |
dc.contributor.author.none.fl_str_mv |
Scott C. Fears Remmelt, Schür Sjouwerman, Rachel Service, Susan K Araya, Carmen Araya, Xinia Bejarano, Julio Knowles, Emma Gomez-Makhinson, Juliana López Tobón, María Cecilia Aldana, Ileana Teshiba, Terri M. Abaryan, Zvart Al-Sharif, Noor B. Navarro, Linda Tishler, Todd A. Altshuler, Lori Bartzokis, George Escobar, Javier I. Glahn, David C. Thompson, Paul M. Lopez-Jaramillo, Carlos Macaya, Gabriel Molina, Julio Reus, Victor I. Sabatti, Chiara |
dc.subject.decs.none.fl_str_mv |
Trastorno Bipolar Bipolar Disorder Genealogía y Heráldica Genealogy and Heraldry Temperamento Temperament Imagen por Resonancia Magnética Magnetic Resonance Imaging |
topic |
Trastorno Bipolar Bipolar Disorder Genealogía y Heráldica Genealogy and Heraldry Temperamento Temperament Imagen por Resonancia Magnética Magnetic Resonance Imaging Fenotipos Phenotype |
dc.subject.lemb.none.fl_str_mv |
Fenotipos Phenotype |
description |
ABSTRACT: Recent theories regarding the pathophysiology of bipolar disorder suggest contributions of both neurodevelopmental and neurodegenerative processes. While structural neuroimaging studies indicate disease-associated neuroanatomical alterations, the behavioural correlates of these alterations have not been well characterized. Here, we investigated multi-generational families genetically enriched for bipolar disorder to: (i) characterize neurobehavioural correlates of neuroanatomical measures implicated in the pathophysiology of bipolar disorder; (ii) identify brain–behaviour associations that differ between diagnostic groups; (iii) identify neurocognitive traits that show evidence of accelerated ageing specifically in subjects with bipolar disorder; and (iv) identify brain–behaviour correlations that differ across the age span. Structural neuroimages and multi-dimensional assessments of temperament and neurocognition were acquired from 527 (153 bipolar disorder and 374 non-bipolar disorder) adults aged 18–87 years in 26 families with heavy genetic loading for bipolar disorder. We used linear regression models to identify significant brain–behaviour associations and test whether brain–behaviour relationships differed: (i) between diagnostic groups; and (ii) as a function of age. We found that total cortical and ventricular volume had the greatest number of significant behavioural associations, and included correlations with measures from multiple cognitive domains, particularly declarative and working memory and executive function. Cortical thickness measures, in contrast, showed more specific associations with declarative memory, letter fluency and processing speed tasks. While the majority of brain–behaviour relationships were similar across diagnostic groups, increased cortical thickness in ventrolateral prefrontal and parietal cortical regions was associated with better declarative memory only in bipolar disorder subjects, and not in non-bipolar disorder family members. Additionally, while age had a relatively strong impact on all neurocognitive traits, the effects of age on cognition did not differ between diagnostic groups. Most brain–behaviour associations were also similar across the age range, with the exception of cortical and ventricular volume and lingual gyrus thickness, which showed weak correlations with verbal fluency and inhibitory control at younger ages that increased in magnitude in older subjects, regardless of diagnosis. Findings indicate that neuroanatomical traits potentially impacted by bipolar disorder are significantly associated with multiple neurobehavioural domains. Structure–function relationships are generally preserved across diagnostic groups, with the notable exception of ventrolateral prefrontal and parietal association cortex, volumetric increases in which may be associated with cognitive resilience specifically in individuals with bipolar disorder. Although age impacted all neurobehavioural traits, we did not find any evidence of accelerated cognitive decline specific to bipolar disorder subjects. Regardless of diagnosis, greater global brain volume may represent a protective factor for the effects of ageing on executive functioning. |
publishDate |
2015 |
dc.date.issued.none.fl_str_mv |
2015 |
dc.date.accessioned.none.fl_str_mv |
2022-02-07T16:37:33Z |
dc.date.available.none.fl_str_mv |
2022-02-07T16:37:33Z |
dc.type.spa.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.hasversion.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.coar.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.redcol.spa.fl_str_mv |
https://purl.org/redcol/resource_type/ART |
dc.type.local.spa.fl_str_mv |
Artículo de investigación |
format |
http://purl.org/coar/resource_type/c_2df8fbb1 |
status_str |
publishedVersion |
dc.identifier.issn.none.fl_str_mv |
0006-8950 |
dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/10495/25834 |
dc.identifier.doi.none.fl_str_mv |
10.1093/brain/awv106 |
dc.identifier.eissn.none.fl_str_mv |
1460-2156 |
identifier_str_mv |
0006-8950 10.1093/brain/awv106 1460-2156 |
url |
http://hdl.handle.net/10495/25834 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Brain |
dc.rights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by-nc/2.5/co/ |
dc.rights.accessrights.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.creativecommons.spa.fl_str_mv |
https://creativecommons.org/licenses/by-nc/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc/2.5/co/ http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by-nc/4.0/ |
dc.format.extent.spa.fl_str_mv |
16 |
dc.format.mimetype.spa.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Oxford University Press |
dc.publisher.group.spa.fl_str_mv |
Grupo de Investigación en Psiquiatría GIPSI |
dc.publisher.place.spa.fl_str_mv |
Londres, Inglaterra |
institution |
Universidad de Antioquia |
bitstream.url.fl_str_mv |
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MD5 MD5 MD5 |
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Repositorio Institucional Universidad de Antioquia |
repository.mail.fl_str_mv |
andres.perez@udea.edu.co |
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spelling |
Scott C. FearsRemmelt, SchürSjouwerman, RachelService, Susan KAraya, CarmenAraya, XiniaBejarano, JulioKnowles, EmmaGomez-Makhinson, JulianaLópez Tobón, María CeciliaAldana, IleanaTeshiba, Terri M.Abaryan, ZvartAl-Sharif, Noor B.Navarro, LindaTishler, Todd A.Altshuler, LoriBartzokis, GeorgeEscobar, Javier I.Glahn, David C.Thompson, Paul M.Lopez-Jaramillo, CarlosMacaya, GabrielMolina, JulioReus, Victor I.Sabatti, Chiara2022-02-07T16:37:33Z2022-02-07T16:37:33Z20150006-8950http://hdl.handle.net/10495/2583410.1093/brain/awv1061460-2156ABSTRACT: Recent theories regarding the pathophysiology of bipolar disorder suggest contributions of both neurodevelopmental and neurodegenerative processes. While structural neuroimaging studies indicate disease-associated neuroanatomical alterations, the behavioural correlates of these alterations have not been well characterized. Here, we investigated multi-generational families genetically enriched for bipolar disorder to: (i) characterize neurobehavioural correlates of neuroanatomical measures implicated in the pathophysiology of bipolar disorder; (ii) identify brain–behaviour associations that differ between diagnostic groups; (iii) identify neurocognitive traits that show evidence of accelerated ageing specifically in subjects with bipolar disorder; and (iv) identify brain–behaviour correlations that differ across the age span. Structural neuroimages and multi-dimensional assessments of temperament and neurocognition were acquired from 527 (153 bipolar disorder and 374 non-bipolar disorder) adults aged 18–87 years in 26 families with heavy genetic loading for bipolar disorder. We used linear regression models to identify significant brain–behaviour associations and test whether brain–behaviour relationships differed: (i) between diagnostic groups; and (ii) as a function of age. We found that total cortical and ventricular volume had the greatest number of significant behavioural associations, and included correlations with measures from multiple cognitive domains, particularly declarative and working memory and executive function. Cortical thickness measures, in contrast, showed more specific associations with declarative memory, letter fluency and processing speed tasks. While the majority of brain–behaviour relationships were similar across diagnostic groups, increased cortical thickness in ventrolateral prefrontal and parietal cortical regions was associated with better declarative memory only in bipolar disorder subjects, and not in non-bipolar disorder family members. Additionally, while age had a relatively strong impact on all neurocognitive traits, the effects of age on cognition did not differ between diagnostic groups. Most brain–behaviour associations were also similar across the age range, with the exception of cortical and ventricular volume and lingual gyrus thickness, which showed weak correlations with verbal fluency and inhibitory control at younger ages that increased in magnitude in older subjects, regardless of diagnosis. Findings indicate that neuroanatomical traits potentially impacted by bipolar disorder are significantly associated with multiple neurobehavioural domains. Structure–function relationships are generally preserved across diagnostic groups, with the notable exception of ventrolateral prefrontal and parietal association cortex, volumetric increases in which may be associated with cognitive resilience specifically in individuals with bipolar disorder. Although age impacted all neurobehavioural traits, we did not find any evidence of accelerated cognitive decline specific to bipolar disorder subjects. Regardless of diagnosis, greater global brain volume may represent a protective factor for the effects of ageing on executive functioning.COL002914716application/pdfengOxford University PressGrupo de Investigación en Psiquiatría GIPSILondres, Inglaterrainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARTArtículo de investigaciónhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc/2.5/co/http://purl.org/coar/access_right/c_abf2https://creativecommons.org/licenses/by-nc/4.0/Brain structure-function associations in multi-generational families genetically enriched for bipolar disorderTrastorno BipolarBipolar DisorderGenealogía y HeráldicaGenealogy and HeraldryTemperamentoTemperamentImagen por Resonancia MagnéticaMagnetic Resonance ImagingFenotiposPhenotypeBrainBrain208721021387CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8933http://bibliotecadigital.udea.edu.co/bitstream/10495/25834/2/license_rdfc0c92b0ffc8b7d22d9cf56754a416a76MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://bibliotecadigital.udea.edu.co/bitstream/10495/25834/3/license.txt8a4605be74aa9ea9d79846c1fba20a33MD53ORIGINALFearsScott_2015_BrainStructureFunction.pdfFearsScott_2015_BrainStructureFunction.pdfArtículo de investigaciónapplication/pdf986061http://bibliotecadigital.udea.edu.co/bitstream/10495/25834/1/FearsScott_2015_BrainStructureFunction.pdfc4c78369ec809e68a4c5fd8a43f1a261MD5110495/25834oai:bibliotecadigital.udea.edu.co:10495/258342022-02-07 11:37:34.162Repositorio Institucional Universidad de Antioquiaandres.perez@udea.edu.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 |