Functional Connectivity Hypersynchronization in Relatives of Alzheimer’s Disease Patients: An Early E/I Balance Dysfunction?

Author:

Ramírez-Toraño F12,Bruña R123,de Frutos-Lucas J14,Rodríguez-Rojo I C15,Marcos de Pedro S16,Delgado-Losada M L2,Gómez-Ruiz N7,Barabash A89,Marcos A10,López Higes R2,Maestú F123

Affiliation:

1. Laboratory of Cognitive and Computational Neuroscience, Center for Biomedical Technology, Technical University of Madrid, Madrid, Comunidad de Madrid 28223, Spain

2. Department of Experimental Psychology, Universidad Complutense de Madrid, Madrid, Comunidad de Madrid 28223, Spain

3. Networking Research Center on Bioengineering, Biomaterials, and Nanomedicine (CIBER-BBN), Madrid, Comunidad de Madrid 28029, Spain

4. Biological and Health Psychology Department, Universidad Autonoma de Madrid, Madrid, Comunidad de Madrid 28049, Spain

5. Facultad de Psicología, Centro Universitario Villanueva, Madrid, Comunidad de Madrid 28034, Spain

6. Facultad de Educación y Salud, Universidad Camilo José Cela, Madrid, Comunidad de Madrid 28010, Spain

7. Sección Neurorradiología, Servicio de Diagnóstico por Imagen, Hospital Clínico San Carlos, Madrid, Comunidad de Madrid 28040, Spain

8. Endocrinology and Nutrition Department, Hospital Clinico San Carlos and Instituto de Investigación Sanitaria del Hospital Clínico San Carlos, Madrid, Comunidad de Madrid 28040, Spain

9. Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Madrid, Comunidad de Madrid 28029, Spain

10. Neurology Department, Hospital Clinico San Carlos and Instituto de Investigación Sanitaria del Hospital Clínico San Carlos, Madrid, Comunidad de Madrid 28040, Spain

Abstract

Abstract Alzheimer’s disease (AD) studies on animal models, and humans showed a tendency of the brain tissue to become hyperexcitable and hypersynchronized, causing neurodegeneration. However, we know little about either the onset of this phenomenon or its early effects on functional brain networks. We studied functional connectivity (FC) on 127 participants (92 middle-age relatives of AD patients and 35 age-matched nonrelatives) using magnetoencephalography. FC was estimated in the alpha band in areas known both for early amyloid accumulation and disrupted FC in MCI converters to AD. We found a frontoparietal network (anterior cingulate cortex, dorsal frontal, and precuneus) where relatives of AD patients showed hypersynchronization in high alpha (not modulated by APOE-ε4 genotype) in comparison to age-matched nonrelatives. These results represent the first evidence of neurophysiological events causing early network disruption in humans, opening a new perspective for intervention on the excitation/inhibition unbalance.

Funder

Ministry of Economy and Competitiveness

project Neurocentro

Community of Madrid and La Caixa Foundation

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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