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Status: Bibliographieeintrag

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Verfasst von:Meier, Sandra Melanie [VerfasserIn]   i
 Demirakça, Traute [VerfasserIn]   i
 Brusniak, Wencke [VerfasserIn]   i
 Wolf, Isabella [VerfasserIn]   i
 Liebsch, Kristin [VerfasserIn]   i
 Tunç-Skarka, Nuran [VerfasserIn]   i
 Nieratschker, Vanessa [VerfasserIn]   i
 Witt, Stephanie [VerfasserIn]   i
 Matthäus, Franziska [VerfasserIn]   i
 Ende, Gabriele [VerfasserIn]   i
 Flor, Herta [VerfasserIn]   i
 Rietschel, Marcella [VerfasserIn]   i
 Diener, Carsten [VerfasserIn]   i
 Schulze, Thomas Gerd [VerfasserIn]   i
Titel:SCN1A affects brain structure and the neural activity of the aging brain
Verf.angabe:Sandra Meier, Traute Demirakca, Wencke Brusniak, Isabella Wolf, Kristin Liebsch, Nuran Tunc-Skarka, Vanessa Nieratschker, Stephanie H. Witt, Franziska Matthäus, Gabriele Ende, Herta Flor, Marcella Rietschel, Carsten Diener, and Thomas G. Schulze
E-Jahr:2012
Jahr:23 April 2012
Umfang:7 S.
Fussnoten:Gesehen am 23.11.2018
Titel Quelle:Enthalten in: Biological psychiatry
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1985
Jahr Quelle:2012
Band/Heft Quelle:72(2012), 8, Seite 677-683
ISSN Quelle:1873-2402
Abstract:Background: The aging of the human brain is accompanied by changes in cortical structure as well as functional activity and variable degrees of cognitive decline. One-third of the observable inter-individual differences in cognitive decline are thought to be heritable. SCN1A encodes the sodium channel α subunit and is considered to be a susceptibility gene for several neurological disorders with prominent cognitive deficits. In a recent genome-wide association study the C allele of the SCN1A variant rs10930201 was observed to be significantly associated with poor short-term memory performance. rs10930201 was further observed to be related to differences in neural activity during a working memory task. Methods: The aim of the present study was to explore whether SCN1A modifies the vulnerability to aging processes of the human brain. Therefore we assessed the interacting effects of the SCN1A vulnerability allele rs10930201 and age in terms of brain activity and brain morphology in 62 healthy volunteers between 21 and 82 years of age. Results: In C allele carriers, activity in the right inferior frontal cortex and the posterior cingulate cortex increased with age. Moreover, exploratory analysis revealed regional effects of rs10930201 on brain structure, indicating reduced gray matter densities in the frontal and insular regions in the C allele carriers. Conclusions: Collectively, the present results suggest that the SCN1A polymorphism has modulatory effects on brain morphology and vulnerability to age-related alterations in brain activity of cortical regions that subserve working memory.
DOI:doi:10.1016/j.biopsych.2012.03.017
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: http://dx.doi.org/10.1016/j.biopsych.2012.03.017
 Volltext: http://www.sciencedirect.com/science/article/pii/S0006322312002661
 DOI: https://doi.org/10.1016/j.biopsych.2012.03.017
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Aging
 cognition
 frontal cortex
 posterior cingulate cortex
 working memory
K10plus-PPN:1584480254
Verknüpfungen:→ Zeitschrift

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