White Matter Changes Compromise Prefrontal Cortex Function in Healthy Elderly Individuals

Changes in memory function in elderly individuals are often attributed to dysfunction of the prefrontal cortex (PFC). One mechanism for this dysfunction may be disruption of white matter tracts that connect the PFC with its anatomical targets. Here, we tested the hypothesis that white matter degeneration is associated with reduced prefrontal activation. We used white matter hyperintensities (WMH), a magnetic resonance imaging (MRI) finding associated with cerebrovascular disease in elderly individuals, as a marker for white matter degeneration. Specifically, we used structural MRI to quantify the extent of WMH in a group of cognitively normal elderly individuals and tested whether these measures were predictive of the magnitude of prefrontal activity (fMRI) observed during performance of an episodic retrieval task and a verbal working memory task. We also examined the effects of WMH located in the dorsolateral frontal regions with the hypothesis that dorsal PFC WMH would be strongly associated with not only PFC function, but also with areas that are anatomically and functionally linked to the PFC in a task-dependent manner. Results showed that increases in both global and regional dorsal PFC WMH volume were associated with decreases in PFC activity. In addition, dorsal PFC WMH volume was associated with decreased activity in medial temporal and anterior cingulate regions during episodic retrieval and decreased activity in the posterior parietal and anterior cingulate cortex during working memory performance. These results suggest that disruption of white matter tracts, especially within the PFC, may be a mechanism for age-related changes in memory functioning.

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

[2]  J. Jonides,et al.  Storage and executive processes in the frontal lobes. , 1999, Science.

[3]  R. Marshall,et al.  Chronic ischemia and neurocognition. , 2007, Neuroimaging clinics of North America.

[4]  B. Horwitz,et al.  Method for quantification of brain, ventricular, and subarachnoid CSF volumes from MR images. , 1992, Journal of computer assisted tomography.

[5]  C. Grady Functional brain imaging and age-related changes in cognition , 2000, Biological Psychology.

[6]  D. Teichberg,et al.  Local histogram correction of MRI spatially dependent image pixel intensity nonuniformity , 1996, Journal of magnetic resonance imaging : JMRI.

[7]  Marcia K. Johnson,et al.  Prefrontal activity associated with working memory and episodic long-term memory , 2003, Neuropsychologia.

[8]  C. Mateer,et al.  A Review of the Stereotype Threat Literature and Its Application in a Neurological Population , 2008, Neuropsychology Review.

[9]  D. Head,et al.  Differential vulnerability of anterior white matter in nondemented aging with minimal acceleration in dementia of the Alzheimer type: evidence from diffusion tensor imaging. , 2004, Cerebral cortex.

[10]  Giovanni B. Frisoni,et al.  White matter lesions in the elderly: Pathophysiological hypothesis on the effect on brain plasticity and reserve , 2008, Journal of the Neurological Sciences.

[11]  B Horwitz,et al.  X-chromosome effects on female brain: a magnetic resonance imaging study of Turner's syndrome , 1993, The Lancet.

[12]  R. Buckner,et al.  THE COGNITIVE NEUROSCIENCE OF REMEMBERING , 2001 .

[13]  P. Goldman-Rakic,et al.  Inactivation of parietal and prefrontal cortex reveals interdependence of neural activity during memory-guided saccades. , 2000, Journal of neurophysiology.

[14]  R. Cabeza Hemispheric asymmetry reduction in older adults: the HAROLD model. , 2002, Psychology and aging.

[15]  Karen M Rodrigue,et al.  Hypertension and the brain: vulnerability of the prefrontal regions and executive functions. , 2003, Behavioral neuroscience.

[16]  A. Wagner,et al.  Prefrontal and hippocampal contributions to visual associative recognition: Interactions between cognitive control and episodic retrieval , 2004, Brain and Cognition.

[17]  Cheryl L Grady,et al.  Changes in memory processing with age , 2000, Current Opinion in Neurobiology.

[18]  A Pfefferbaum,et al.  Neuroradiological characterization of normal adult ageing. , 2007, The British journal of radiology.

[19]  Fergus I M Craik,et al.  Relations between source amnesia and frontal lobe functioning in older adults. , 1990, Psychology and aging.

[20]  Eric E. Smith,et al.  Cerebral White Matter , 2008, Annals of the New York Academy of Sciences.

[21]  L. Bronge,et al.  Magnetic resonance imaging in dementia: a study of brain white matter changes , 2002 .

[22]  K. Kiehl,et al.  Removal of Confounding Effects of Global Signal in Functional MRI Analyses , 2001, NeuroImage.

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

[24]  Danielle J. Tisserand,et al.  On the Involvement of Prefrontal Networks in Cognitive Ageing , 2003, Cortex.

[25]  Yaakov Stern,et al.  Aging Does Not Affect Brain Patterns of Repetition Effects Associated with Perceptual Priming of Novel Objects , 2008, Journal of Cognitive Neuroscience.

[26]  Adrian M. Owen,et al.  Inefficiency in Self-organized Attentional Switching in the Normal Aging Population is Associated with Decreased Activity in the Ventrolateral Prefrontal Cortex , 2008, Journal of Cognitive Neuroscience.

[27]  Hidenao Fukuyama,et al.  Functional roles of the cingulo-frontal network in performance on working memory , 2004, NeuroImage.

[28]  J M Wardlaw,et al.  Prevalence of cerebral white matter lesions in elderly people: a population based magnetic resonance imaging study: the Rotterdam Scan Study , 2001, Journal of neurology, neurosurgery, and psychiatry.

[29]  Albert Hofman,et al.  Cognitive Correlates of Ventricular Enlargement and Cerebral White Matter Lesions on Magnetic Resonance Imaging: The Rotterdam Study , 1994, Stroke.

[30]  D. Salat,et al.  Prefrontal gray and white matter volumes in healthy aging and Alzheimer disease. , 1999, Archives of neurology.

[31]  Gary H. Glover,et al.  Variable effects of aging on frontal lobe contributions to memory , 2002, Neuroreport.

[32]  K Yaffe,et al.  Different patterns of N-acetylaspartate loss in subcortical ischemic vascular dementia and AD , 2003, Neurology.

[33]  Lars-Göran Nilsson,et al.  High Prevalence of White Matter Hyperintensities in Normal Aging: Relation to Blood Pressure and Cognition , 2003, Cortex.

[34]  P. Pietrini,et al.  Sex differences in human brain morphometry and metabolism: an in vivo quantitative magnetic resonance imaging and positron emission tomography study on the effect of aging. , 1996, Archives of general psychiatry.

[35]  Cheryl L Grady,et al.  Age‐related differences in the functional connectivity of the hippocampus during memory encoding , 2003, Hippocampus.

[36]  P. Scheltens,et al.  Distortions in rest–activity rhythm in aging relate to white matter hyperintensities , 2008, Neurobiology of Aging.

[37]  D. Head,et al.  Selective aging of the human cerebral cortex observed in vivo: differential vulnerability of the prefrontal gray matter. , 1997, Cerebral cortex.

[38]  Wei Wen,et al.  The topography of white matter hyperintensities on brain MRI in healthy 60- to 64-year-old individuals , 2004, NeuroImage.

[39]  P. Goldman-Rakic,et al.  Common cortical and subcortical targets of the dorsolateral prefrontal and posterior parietal cortices in the rhesus monkey: evidence for a distributed neural network subserving spatially guided behavior , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[40]  F. Gunning-Dixon,et al.  The cognitive correlates of white matter abnormalities in normal aging: a quantitative review. , 2000, Neuropsychology.

[41]  M H Buonocore,et al.  Hippocampal, parahippocampal and occipital-temporal contributions to associative and item recognition memory: an fMRI study , 2001, Neuroreport.

[42]  M D'Esposito,et al.  The roles of prefrontal brain regions in components of working memory: effects of memory load and individual differences. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[43]  R. Cabeza,et al.  Imaging Cognition II: An Empirical Review of 275 PET and fMRI Studies , 2000, Journal of Cognitive Neuroscience.

[44]  Karl J. Friston,et al.  A Voxel-Based Morphometric Study of Ageing in 465 Normal Adult Human Brains , 2001, NeuroImage.

[45]  M. O’Sullivan,et al.  Activate your online subscription , 2001, Neurology.

[46]  L. Gjerstad,et al.  White matter lesion severity is associated with reduced cognitive performances in patients with normal CSF Aβ42 levels , 2008, Acta neurologica Scandinavica.

[47]  B Horwitz,et al.  Age-related differences in volumes of subcortical nuclei, brain matter, and cerebrospinal fluid in healthy men as measured with magnetic resonance imaging. , 1992, Archives of neurology.

[48]  Charles DeCarli,et al.  Different mechanisms of episodic memory failure in mild cognitive impairment , 2005, Neuropsychologia.

[49]  Sarah E. MacPherson,et al.  Age, executive function, and social decision making: a dorsolateral prefrontal theory of cognitive aging. , 2002, Psychology and aging.

[50]  A. Dale,et al.  Thinning of the cerebral cortex in aging. , 2004, Cerebral cortex.

[51]  M. Fabiani,et al.  Use it or lose it? SES mitigates age-related decline in a recency/recognition task , 2008, Neurobiology of Aging.

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

[53]  Philip Scheltens,et al.  White Matter Hyperintensities and Working Memory: An Explorative Study , 2008, Neuropsychology, development, and cognition. Section B, Aging, neuropsychology and cognition.

[54]  H. C. Chui,et al.  White matter lesions impair frontal lobe function regardless of their location , 2004, Neurology.

[55]  M. Botvinick,et al.  The Contribution of the Anterior Cingulate Cortex to Executive Processes in Cognition , 1999, Reviews in the neurosciences.

[56]  J. Logan,et al.  Under-Recruitment and Nonselective Recruitment Dissociable Neural Mechanisms Associated with Aging , 2002, Neuron.

[57]  J. Haxby,et al.  The effect of white matter hyperintensity volume on brain structure, cognitive performance, and cerebral metabolism of glucose in 51 healthy adults , 1995, Neurology.

[58]  M H Buonocore,et al.  Brain structure and cognition in a community sample of elderly Latinos , 2002, Neurology.