Human aging magnifies genetic effects on executive functioning and working memory

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Irene E. Nagel - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) (Autor:in)
  • Christian Chicherio - , Max Planck Institute for Human Development (Autor:in)
  • Shu Chen Li - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) (Autor:in)
  • Timo von Oertzen - , Max Planck Institute for Human Development (Autor:in)
  • Thomas Sander - , Max-Delbrück-Centrum für Molekulare Medizin (MDC) (Autor:in)
  • Arno Villringer - , Berlin Center for Advanced Neuroimaging (BCAN) , Charité – Universitätsmedizin Berlin, Max-Planck-Institut für Kognitions- und Neurowissenschaften (Autor:in)
  • Hauke R. Heekeren - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) , Charité – Universitätsmedizin Berlin, Max-Planck-Institut für Kognitions- und Neurowissenschaften (Autor:in)
  • Lars Bäckman - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) , Aging Research Center (ARC) (Autor:in)
  • Ulman Lindenberger - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) (Autor:in)

Abstract

We demonstrate that common genetic polymorphisms contribute to the increasing heterogeneity of cognitive functioning in old age. We assess two common Val/Met polymorphisms, one affecting the Catechol-O-Methyltransferase (COMT) enzyme, which degrades dopamine (DA) in prefrontal cortex (PFC), and the other influencing the brain-derived neurotrophic factor (BDNF) protein. In two tasks (Wisconsin Card Sorting and spatial working memory), we find that effects of COMT genotype on cognitive performance are magnified in old age and modulated by BDNF genotype. Older COMT Val homozygotes showed particularly low levels of performance if they were also BDNF Met carriers. The age-associated magnification of COMT gene effects provides novel information on the inverted U-shaped relation linking dopaminergic neuromodulation in PFC to cognitive performance. The modulation of COMT effects by BDNF extends recent evidence of close interactions between frontal and medial-temporal circuitries in executive functioning and working memory.

Details

OriginalspracheEnglisch
Aufsatznummer1
FachzeitschriftFrontiers in human neuroscience
Jahrgang2
PublikationsstatusVeröffentlicht - 3 Mai 2008
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

ORCID /0000-0001-8409-5390/work/142254947

Schlagworte

Ziele für nachhaltige Entwicklung

Schlagwörter

  • Aging, Dopamine, Executive functions, Genes, Prefrontal cortex

Bibliotheksschlagworte