Neuronal Hyperactivation in EEG Data during Cognitive Tasks Is Related to the Apolipoprotein J/Clusterin Genotype in Nondemented Adults

Author:

Ponomareva Natalya V.12,Andreeva Tatiana V.234,Protasova Maria S.3ORCID,Kunizheva Svetlana S.23,Kuznetsova Irina L.23ORCID,Kolesnikova Ekaterina P.1,Malina Daria D.1,Mitrofanov Andrey A.5,Fokin Vitaly F.1,Illarioshkin Sergey N.1ORCID,Rogaev Evgeny I.26

Affiliation:

1. Research Center of Neurology, 125367 Moscow, Russia

2. Center for Genetics and Life Science, Sirius University of Science and Technology, 354349 Sochi, Russia

3. Vavilov Institute of General Genetics, Russian Academy of Sciences, 119991 Moscow, Russia

4. Centre for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, 119192 Moscow, Russia

5. Research Center of Mental Health, 115522 Moscow, Russia

6. Department of Psychiatry, Umass Chan Medical School, Shrewsbury, MA 01545, USA

Abstract

The clusterin (CLU) rs11136000 CC genotype is a probable risk factor for Alzheimer’s disease (AD). CLU, also known as the apolipoprotein J gene, shares certain properties with the apolipoprotein E (APOE) gene with a well-established relationship with AD. This study aimed to determine whether the electrophysiological patterns of brain activation during the letter fluency task (LFT) depend on CLU genotypes in adults without dementia. Previous studies have shown that LFT performance involves activation of the frontal cortex. We examined EEG alpha1 and alpha2 band desynchronization in the frontal regions during the LFT in 94 nondemented individuals stratified by CLU (rs11136000) genotype. Starting at 30 years of age, CLU CC carriers exhibited more pronounced task-related alpha2 desynchronization than CLU CT&TT carriers in the absence of any differences in LFT performance. In CLU CC carriers, alpha2 desynchronization was significantly correlated with age. Increased task-related activation in individuals at genetic risk for AD may reflect greater “effort” to perform the task and/or neuronal hyperexcitability. The results show that the CLU genotype is associated with neuronal hyperactivation in the frontal cortex during cognitive tasks performances in nondemented individuals, suggesting systematic vulnerability of LFT related cognitive networks in people carrying unfavorable CLU alleles.

Funder

Russian Science Foundation

Ministry of Science and Higher Education of the Russian Federation

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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