BDNF Val66Met Polymorphism and Gamma Band Disruption in Resting State Brain Functional Connectivity: A Magnetoencephalography Study in Cognitively Intact Older Females

The pathophysiological processes undermining brain functioning decades before the onset of the clinical symptoms associated with dementia are still not well understood. Several heritability studies have reported that the Brain Derived Neurotrophic Factor (BDNF) Val66Met genetic polymorphism could co...

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Main Authors: Inmaculada C. Rodríguez-Rojo, Pablo Cuesta, María Eugenia López, Jaisalmer de Frutos-Lucas, Ricardo Bruña, Ernesto Pereda, Ana Barabash, Pedro Montejo, Mercedes Montenegro-Peña, Alberto Marcos, Ramón López-Higes, Alberto Fernández, Fernando Maestú
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-10-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnins.2018.00684/full
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author Inmaculada C. Rodríguez-Rojo
Inmaculada C. Rodríguez-Rojo
Pablo Cuesta
Pablo Cuesta
María Eugenia López
María Eugenia López
Jaisalmer de Frutos-Lucas
Jaisalmer de Frutos-Lucas
Ricardo Bruña
Ricardo Bruña
Ricardo Bruña
Ernesto Pereda
Ernesto Pereda
Ana Barabash
Ana Barabash
Pedro Montejo
Mercedes Montenegro-Peña
Alberto Marcos
Ramón López-Higes
Alberto Fernández
Alberto Fernández
Fernando Maestú
Fernando Maestú
Fernando Maestú
author_facet Inmaculada C. Rodríguez-Rojo
Inmaculada C. Rodríguez-Rojo
Pablo Cuesta
Pablo Cuesta
María Eugenia López
María Eugenia López
Jaisalmer de Frutos-Lucas
Jaisalmer de Frutos-Lucas
Ricardo Bruña
Ricardo Bruña
Ricardo Bruña
Ernesto Pereda
Ernesto Pereda
Ana Barabash
Ana Barabash
Pedro Montejo
Mercedes Montenegro-Peña
Alberto Marcos
Ramón López-Higes
Alberto Fernández
Alberto Fernández
Fernando Maestú
Fernando Maestú
Fernando Maestú
author_sort Inmaculada C. Rodríguez-Rojo
collection DOAJ
description The pathophysiological processes undermining brain functioning decades before the onset of the clinical symptoms associated with dementia are still not well understood. Several heritability studies have reported that the Brain Derived Neurotrophic Factor (BDNF) Val66Met genetic polymorphism could contribute to the acceleration of cognitive decline in aging. This mutation may affect brain functional connectivity (FC), especially in those who are carriers of the BDNF Met allele. The aim of this work was to explore the influence of the BDNF Val66Met polymorphism in whole brain eyes-closed, resting-state magnetoencephalography (MEG) FC in a sample of 36 cognitively intact (CI) older females. All of them were ε3ε3 homozygotes for the apolipoprotein E (APOE) gene and were divided into two subgroups according to the presence of the Met allele: Val/Met group (n = 16) and Val/Val group (n = 20). They did not differ in age, years of education, Mini-Mental State Examination scores, or normalized hippocampal volumes. Our results showed reduced antero-posterior gamma band FC within the Val/Met genetic risk group, which may be caused by a GABAergic network impairment. Despite the lack of cognitive decline, these results might suggest a selective brain network vulnerability due to the carriage of the BDNF Met allele, which is linked to a potential progression to dementia. This neurophysiological signature, as tracked with MEG FC, indicates that age-related brain functioning changes could be mediated by the influence of particular genetic risk factors.
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spelling doaj.art-b6dc7b936d654c0284be5ad1d4a646bb2022-12-21T18:43:41ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2018-10-011210.3389/fnins.2018.00684401630BDNF Val66Met Polymorphism and Gamma Band Disruption in Resting State Brain Functional Connectivity: A Magnetoencephalography Study in Cognitively Intact Older FemalesInmaculada C. Rodríguez-Rojo0Inmaculada C. Rodríguez-Rojo1Pablo Cuesta2Pablo Cuesta3María Eugenia López4María Eugenia López5Jaisalmer de Frutos-Lucas6Jaisalmer de Frutos-Lucas7Ricardo Bruña8Ricardo Bruña9Ricardo Bruña10Ernesto Pereda11Ernesto Pereda12Ana Barabash13Ana Barabash14Pedro Montejo15Mercedes Montenegro-Peña16Alberto Marcos17Ramón López-Higes18Alberto Fernández19Alberto Fernández20Fernando Maestú21Fernando Maestú22Fernando Maestú23Laboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Universidad Complutense and Universidad Politécnica de Madrid, Madrid, SpainDepartment of Experimental Psychology, Cognitive Processes and Speech Therapy, Universidad Complutense de Madrid, Madrid, SpainLaboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Universidad Complutense and Universidad Politécnica de Madrid, Madrid, SpainElectrical Engineering and Bioengineering Lab, Department of Industrial Engineering and IUNE, Universidad de La Laguna, Tenerife, SpainLaboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Universidad Complutense and Universidad Politécnica de Madrid, Madrid, SpainDepartment of Experimental Psychology, Cognitive Processes and Speech Therapy, Universidad Complutense de Madrid, Madrid, SpainLaboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Universidad Complutense and Universidad Politécnica de Madrid, Madrid, SpainBiological and Health Psychology Department, Universidad Autónoma de Madrid, Madrid, SpainLaboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Universidad Complutense and Universidad Politécnica de Madrid, Madrid, SpainDepartment of Experimental Psychology, Cognitive Processes and Speech Therapy, Universidad Complutense de Madrid, Madrid, SpainNetworking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Madrid, SpainLaboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Universidad Complutense and Universidad Politécnica de Madrid, Madrid, SpainElectrical Engineering and Bioengineering Lab, Department of Industrial Engineering and IUNE, Universidad de La Laguna, Tenerife, SpainLaboratory of Psychoneuroendocrinology and Genetics, Hospital Clínico San Carlos, Madrid, SpainInstituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, SpainCenter for the Prevention of Cognitive Impairment, Public Health Institute, Madrid-Salud, Madrid, SpainCenter for the Prevention of Cognitive Impairment, Public Health Institute, Madrid-Salud, Madrid, SpainNeurology Department, Hospital Clínico San Carlos, Madrid, SpainDepartment of Experimental Psychology, Cognitive Processes and Speech Therapy, Universidad Complutense de Madrid, Madrid, SpainLaboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Universidad Complutense and Universidad Politécnica de Madrid, Madrid, Spain0Department of Legal Medicine, Psychiatry, and Pathology, Universidad Complutense de Madrid, Madrid, SpainLaboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Universidad Complutense and Universidad Politécnica de Madrid, Madrid, SpainDepartment of Experimental Psychology, Cognitive Processes and Speech Therapy, Universidad Complutense de Madrid, Madrid, SpainNetworking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Madrid, SpainThe pathophysiological processes undermining brain functioning decades before the onset of the clinical symptoms associated with dementia are still not well understood. Several heritability studies have reported that the Brain Derived Neurotrophic Factor (BDNF) Val66Met genetic polymorphism could contribute to the acceleration of cognitive decline in aging. This mutation may affect brain functional connectivity (FC), especially in those who are carriers of the BDNF Met allele. The aim of this work was to explore the influence of the BDNF Val66Met polymorphism in whole brain eyes-closed, resting-state magnetoencephalography (MEG) FC in a sample of 36 cognitively intact (CI) older females. All of them were ε3ε3 homozygotes for the apolipoprotein E (APOE) gene and were divided into two subgroups according to the presence of the Met allele: Val/Met group (n = 16) and Val/Val group (n = 20). They did not differ in age, years of education, Mini-Mental State Examination scores, or normalized hippocampal volumes. Our results showed reduced antero-posterior gamma band FC within the Val/Met genetic risk group, which may be caused by a GABAergic network impairment. Despite the lack of cognitive decline, these results might suggest a selective brain network vulnerability due to the carriage of the BDNF Met allele, which is linked to a potential progression to dementia. This neurophysiological signature, as tracked with MEG FC, indicates that age-related brain functioning changes could be mediated by the influence of particular genetic risk factors.https://www.frontiersin.org/article/10.3389/fnins.2018.00684/fullBDNF Val66Metmagnetoencephalographygamma rhythmscognitive functioninghealthy agingAlzheimer's disease
spellingShingle Inmaculada C. Rodríguez-Rojo
Inmaculada C. Rodríguez-Rojo
Pablo Cuesta
Pablo Cuesta
María Eugenia López
María Eugenia López
Jaisalmer de Frutos-Lucas
Jaisalmer de Frutos-Lucas
Ricardo Bruña
Ricardo Bruña
Ricardo Bruña
Ernesto Pereda
Ernesto Pereda
Ana Barabash
Ana Barabash
Pedro Montejo
Mercedes Montenegro-Peña
Alberto Marcos
Ramón López-Higes
Alberto Fernández
Alberto Fernández
Fernando Maestú
Fernando Maestú
Fernando Maestú
BDNF Val66Met Polymorphism and Gamma Band Disruption in Resting State Brain Functional Connectivity: A Magnetoencephalography Study in Cognitively Intact Older Females
Frontiers in Neuroscience
BDNF Val66Met
magnetoencephalography
gamma rhythms
cognitive functioning
healthy aging
Alzheimer's disease
title BDNF Val66Met Polymorphism and Gamma Band Disruption in Resting State Brain Functional Connectivity: A Magnetoencephalography Study in Cognitively Intact Older Females
title_full BDNF Val66Met Polymorphism and Gamma Band Disruption in Resting State Brain Functional Connectivity: A Magnetoencephalography Study in Cognitively Intact Older Females
title_fullStr BDNF Val66Met Polymorphism and Gamma Band Disruption in Resting State Brain Functional Connectivity: A Magnetoencephalography Study in Cognitively Intact Older Females
title_full_unstemmed BDNF Val66Met Polymorphism and Gamma Band Disruption in Resting State Brain Functional Connectivity: A Magnetoencephalography Study in Cognitively Intact Older Females
title_short BDNF Val66Met Polymorphism and Gamma Band Disruption in Resting State Brain Functional Connectivity: A Magnetoencephalography Study in Cognitively Intact Older Females
title_sort bdnf val66met polymorphism and gamma band disruption in resting state brain functional connectivity a magnetoencephalography study in cognitively intact older females
topic BDNF Val66Met
magnetoencephalography
gamma rhythms
cognitive functioning
healthy aging
Alzheimer's disease
url https://www.frontiersin.org/article/10.3389/fnins.2018.00684/full
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