4.6 Article

Failure to Modulate Attentional Control in Advanced Aging Linked to White Matter Pathology

Journal

CEREBRAL CORTEX
Volume 22, Issue 5, Pages 1038-1051

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhr172

Keywords

aging; amyloid beta; executive function; fMRI; individual differences; PET

Categories

Funding

  1. National Institute on Aging [R01 AG021910, R01 AG034556, R01 AG037497, P01 AG036694, R01 AG027435-S1, 5 P01 AG04390]
  2. Howard Hughes Medical Institute
  3. Alzheimer's Association
  4. Netherlands Organization for Scientific Research
  5. National Center for Research Resources (NCRR), National Institutes of Health
  6. NCRR [1S10RR023401, 1S10RR019307, 1S10RR023043]
  7. Hebrew SeniorLife Institute for Aging Research
  8. Massachusetts Alzheimer's Disease Research Center [2 P50 AG05134]

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Advanced aging is associated with reduced attentional control and less flexible information processing. Here, the origins of these cognitive effects were explored using a functional magnetic resonance imaging task that systematically varied demands to shift attention and inhibit irrelevant information across task blocks. Prefrontal and parietal regions previously implicated in attentional control were recruited by the task and most so for the most demanding task configurations. A subset of older individuals did not modulate activity in frontal and parietal regions in response to changing task requirements. Older adults who did not dynamically modulate activity underperformed their peers and scored more poorly on neuropsychological measures of executive function and speed of processing. Examining 2 markers of preclinical pathology in older adults revealed that white matter hyperintensities (WMHs), but not high amyloid burden, were associated with failure to modulate activity in response to changing task demands. In contrast, high amyloid burden was associated with alterations in default network activity. These results suggest failure to modulate frontal and parietal activity reflects a disruptive process in advanced aging associated with specific neuropathologic processes.

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