Human Aging Magnifies Genetic Effects on Executive Functioning and Working Memory

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.

[1]  C. Grady Cognitive Neuroscience of Aging , 2008, Annals of the New York Academy of Sciences.

[2]  M. Reuter,et al.  Genetically Determined Differences in Learning from Errors , 2007, Science.

[3]  R. Kessels,et al.  Spatial and non-spatial contextual working memory in patients with diencephalic or hippocampal dysfunction , 2007, Brain Research.

[4]  A. Diamond Consequences of variations in genes that affect dopamine in prefrontal cortex. , 2007, Cerebral cortex.

[5]  Andreas Meyer-Lindenberg,et al.  Epistasis between catechol-O-methyltransferase and type II metabotropic glutamate receptor 3 genes on working memory brain function , 2007, Proceedings of the National Academy of Sciences.

[6]  Cindy M. de Frias,et al.  Revisiting the dedifferentiation hypothesis with longitudinal multi-cohort data. , 2007 .

[7]  I. Deary,et al.  COMT genotype and cognitive ability: A longitudinal aging study , 2007, Neuroscience Letters.

[8]  J. Gläscher,et al.  Gene–gene interaction associated with neural reward sensitivity , 2007, Proceedings of the National Academy of Sciences.

[9]  A. Grace,et al.  Regulation of firing of dopaminergic neurons and control of goal-directed behaviors , 2007, Trends in Neurosciences.

[10]  Andreas Meyer-Lindenberg,et al.  Genetic evidence implicating DARPP-32 in human frontostriatal structure, function, and cognition. , 2007, The Journal of clinical investigation.

[11]  H. Flor,et al.  Gene–gene effects on central processing of aversive stimuli , 2007, Molecular Psychiatry.

[12]  T. Robbins,et al.  Effects of the catechol-O-methyltransferase Val158Met polymorphism on executive function: a meta-analysis of the Wisconsin Card Sort Test in schizophrenia and healthy controls , 2007, Molecular Psychiatry.

[13]  Yoshiro Okubo,et al.  Memory and frontal lobe functions; possible relations with dopamine D2 receptors in the hippocampus , 2007, NeuroImage.

[14]  Graham V. Williams,et al.  Inverted-U dopamine D1 receptor actions on prefrontal neurons engaged in working memory , 2007, Nature Neuroscience.

[15]  Karen M Rodrigue,et al.  Brain Aging and Its Modifiers , 2007, Annals of the New York Academy of Sciences.

[16]  J. Mill,et al.  Family‐based association study between brain‐derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples , 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[17]  L. Nyberg,et al.  The correlative triad among aging, dopamine, and cognition: Current status and future prospects , 2006, Neuroscience & Biobehavioral Reviews.

[18]  A. Meyer-Lindenberg,et al.  Prefrontal-Hippocampal Coupling During Memory Processing Is Modulated by COMT Val158Met Genotype , 2006, Biological Psychiatry.

[19]  T. Wassink,et al.  Cognitive and magnetic resonance imaging brain morphometric correlates of brain-derived neurotrophic factor Val66Met gene polymorphism in patients with schizophrenia and healthy volunteers. , 2006, Archives of general psychiatry.

[20]  Anjan Chatterjee,et al.  Visual Working Memory Is Impaired when the Medial Temporal Lobe Is Damaged , 2006, Journal of Cognitive Neuroscience.

[21]  Thomas E. Nichols,et al.  Impact of complex genetic variation in COMT on human brain function , 2006, Molecular Psychiatry.

[22]  J. Savitz,et al.  The molecular genetics of cognition: dopamine, COMT and BDNF , 2006, Genes, brain, and behavior.

[23]  I. Deary,et al.  The brain-derived neurotrophic factor Val66Met polymorphism is associated with age-related change in reasoning skills , 2006, Molecular Psychiatry.

[24]  Robert Plomin,et al.  Generalist genes: implications for the cognitive sciences , 2006, Trends in Cognitive Sciences.

[25]  A. Meyer-Lindenberg,et al.  Neurophysiological correlates of age-related changes in working memory capacity , 2006, Neuroscience Letters.

[26]  I. Deary,et al.  The functional COMT polymorphism, Val158Met, is associated with logical memory and the personality trait intellect/imagination in a cohort of healthy 79 year olds , 2005, Neuroscience Letters.

[27]  Lars-Göran Nilsson,et al.  Catechol O-Methyltransferase Val158Met Polymorphism is Associated with Cognitive Performance in Nondemented Adults , 2005, Journal of Cognitive Neuroscience.

[28]  L. Nyberg,et al.  Common fronto-parietal activity in attention, memory, and consciousness: Shared demands on integration? , 2005, Consciousness and Cognition.

[29]  H. Arai,et al.  Brain-derived neurotrophic factor gene polymorphisms and Alzheimer’s disease , 2005, Journal of Neural Transmission.

[30]  V. Sheffield,et al.  Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow , 2005, Molecular Psychiatry.

[31]  L. Bäckman,et al.  The role of the striatal dopamine transporter in cognitive aging , 2005, Psychiatry Research: Neuroimaging.

[32]  A. Meyer-Lindenberg,et al.  The Brain-derived Neurotrophic Factor Val66met Polymorphism and Variation in Human Cortical Morphology , 2022 .

[33]  A. Grace,et al.  The Catechol-O-Methyltransferase Polymorphism: Relations to the Tonic–Phasic Dopamine Hypothesis and Neuropsychiatric Phenotypes , 2004, Neuropsychopharmacology.

[34]  Jonathan D. Cohen,et al.  Computational roles for dopamine in behavioural control , 2004, Nature.

[35]  Lars-Göran Nilsson,et al.  COMT Gene Polymorphism Is Associated with Declarative Memory in Adulthood and Old Age , 2004, Behavior genetics.

[36]  T. Goldberg,et al.  Genes and the parsing of cognitive processes , 2004, Trends in Cognitive Sciences.

[37]  S. Tsai,et al.  Association Study of a Functional Catechol-O-Methyltransferase Genetic Polymorphism with Age of Onset, Cognitive Function, Symptomatology and Prognosis in Chronic Schizophrenia , 2004, Neuropsychobiology.

[38]  Florin Dolcos,et al.  Attention-related activity during episodic memory retrieval: a cross-function fMRI study , 2003, Neuropsychologia.

[39]  J. Hauser,et al.  Polymorphism of the brain-derived neurotrophic factor gene and performance on a cognitive prefrontal test in bipolar patients. , 2003, Bipolar disorders.

[40]  M. Egan,et al.  Brain-Derived Neurotrophic Factor val66met Polymorphism Affects Human Memory-Related Hippocampal Activity and Predicts Memory Performance , 2003, The Journal of Neuroscience.

[41]  M. Narita,et al.  Implication of brain-derived neurotrophic factor in the release of dopamine and dopamine-related behaviors induced by methamphetamine , 2003, Neuroscience.

[42]  M. Egan,et al.  Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[43]  Shih-Jen Tsai,et al.  Association study of a functional catechol-O-methyltransferase-gene polymorphism and cognitive function in healthy females , 2003, Neuroscience Letters.

[44]  M. Egan,et al.  The BDNF val66met Polymorphism Affects Activity-Dependent Secretion of BDNF and Human Memory and Hippocampal Function , 2003, Cell.

[45]  Sverker Sikström,et al.  Integrative neurocomputational perspectives on cognitive aging, neuromodulation, and representation , 2002, Neuroscience & Biobehavioral Reviews.

[46]  A. Malhotra,et al.  A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition. , 2002, The American journal of psychiatry.

[47]  S. Sikström,et al.  Aging cognition: from neuromodulation to representation , 2001, Trends in Cognitive Sciences.

[48]  R. Straub,et al.  Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[49]  Lars Farde,et al.  Age-related dopamine D2/D3 receptor loss in extrastriatal regions of the human brain , 2000, Neurobiology of Aging.

[50]  M. D’Esposito,et al.  Isolating the neural mechanisms of age-related changes in human working memory , 2000, Nature Neuroscience.

[51]  R. Dixon,et al.  Age-related cognitive deficits mediated by changes in the striatal dopamine system. , 2000, The American journal of psychiatry.

[52]  S Hale,et al.  Converging evidence that visuospatial cognition is more age-sensitive than verbal cognition. , 2000, Psychology and aging.

[53]  P. Goldman-Rakic,et al.  D1 receptors in prefrontal cells and circuits , 2000, Brain Research Reviews.

[54]  N. Volkow,et al.  Parallel loss of presynaptic and postsynaptic dopamine markers in normal aging , 1998, Annals of neurology.

[55]  P. Roland,et al.  Bilateral activation of fronto-parietal networks by incrementing demand in a working memory task. , 1997, Cerebral cortex.

[56]  Leslie G. Ungerleider,et al.  Transient and sustained activity in a distributed neural system for human working memory , 1997, Nature.

[57]  P. Baltes,et al.  Emergence of a powerful connection between sensory and cognitive functions across the adult life span: a new window to the study of cognitive aging? , 1997, Psychology and aging.

[58]  S. Petersen,et al.  Functional Anatomic Studies of Memory Retrieval for Auditory Words and Visual Pictures , 1996, The Journal of Neuroscience.

[59]  R. West,et al.  An application of prefrontal cortex function theory to cognitive aging. , 1996, Psychological bulletin.

[60]  K. Leenders,et al.  Dopamine D2 Receptors in Normal Human Brain: Effect of Age Measured by Positron Emission Tomography (PET) and [11C]‐Raclopride a , 1993, Annals of the New York Academy of Sciences.

[61]  R. Cabeza,et al.  Frontiers in Human Neuroscience , 2009 .

[62]  Brad E. Sheese,et al.  Attention genes. , 2007, Developmental science.

[63]  G. Mcclearn,et al.  Contextual genetics. , 2006, Trends in genetics : TIG.

[64]  K. Suzuki,et al.  Age-related changes in human D1 dopamine receptors measured by positron emission tomography , 2005, Psychopharmacology.

[65]  A. Diamond,et al.  Genetic and neurochemical modulation of prefrontal cognitive functions in children. , 2004, The American journal of psychiatry.

[66]  Ian J Deary,et al.  The impact of childhood intelligence on later life: following up the Scottish mental surveys of 1932 and 1947. , 2004, Journal of personality and social psychology.

[67]  M. Riva,et al.  Association between the BDNF 196 A/G polymorphism and sporadic Alzheimer's disease , 2002, Molecular Psychiatry.

[68]  E. Miller,et al.  An integrative theory of prefrontal cortex function. , 2001, Annual review of neuroscience.

[69]  U. Staudinger,et al.  Lifespan psychology: theory and application to intellectual functioning. , 1999, Annual review of psychology.

[70]  Maria Larsson,et al.  Cognitive functioning in very old age , 1999 .

[71]  Robert K. Heaton,et al.  Wisconsin Card Sorting Test Manual – Revised and Expanded , 1993 .

[72]  G. E. Alexander,et al.  Parallel organization of functionally segregated circuits linking basal ganglia and cortex. , 1986, Annual review of neuroscience.