Human aging magnifies genetic effects on executive functioning and working memory

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Irene E. Nagel - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) (Author)
  • Christian Chicherio - , Max Planck Institute for Human Development (Author)
  • Shu Chen Li - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) (Author)
  • Timo von Oertzen - , Max Planck Institute for Human Development (Author)
  • Thomas Sander - , Max Delbrück Center for Molecular Medicine (MDC) (Author)
  • Arno Villringer - , Berlin Center for Advanced Neuroimaging (BCAN) , Charité – Universitätsmedizin Berlin, Max Planck Institute for Human Cognitive and Brain Sciences (Author)
  • Hauke R. Heekeren - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) , Charité – Universitätsmedizin Berlin, Max Planck Institute for Human Cognitive and Brain Sciences (Author)
  • Lars Bäckman - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) , Aging Research Center (ARC) (Author)
  • Ulman Lindenberger - , Max Planck Institute for Human Development, Berlin Center for Advanced Neuroimaging (BCAN) (Author)

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

Original languageEnglish
Article number1
JournalFrontiers in human neuroscience
Volume2
Publication statusPublished - 3 May 2008
Peer-reviewedYes
Externally publishedYes

External IDs

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

Keywords

Sustainable Development Goals

Keywords

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

Library keywords