Abstract
Free full text
Functional MRI Assessment of Task-Induced Deactivation of the Default Mode Network in Alzheimer’s Disease and At-Risk Older Individuals
Abstract
Alzheimer’s disease (AD) is the most common form of dementia in old age, and is characterized by prominent impairment of episodic memory. Recent functional imaging studies in AD have demonstrated alterations in a distributed network of brain regions supporting memory function, including regions of the default mode network. Previous positron emission tomography studies of older individuals at risk for AD have revealed hypometabolism of association cortical regions similar to the metabolic abnormalities seen in AD patients. In recent functional magnetic resonance imaging (fMRI) studies of AD, corresponding brain default mode regions have also been found to demonstrate an abnormal fMRI task-induced deactivation response pattern. That is, the relative decreases in fMRI signal normally observed in the default mode regions in healthy subjects performing a cognitive task are not seen in AD patients, or may even be reversed to a paradoxical activation response. Our recent studies have revealed alterations in the pattern of deactivation also in elderly individuals at risk for AD by virtue of their APOE e4 genotype, or evidence of mild cognitive impairment (MCI). In agreement with recent reports from other groups, these studies demonstrate that the pattern of fMRI task-induced deactivation is progressively disrupted along the continuum from normal aging to MCI and to clinical AD and more impaired in e4 carriers compared to non-carriers. These findings will be discussed in the context of current literature regarding functional imaging of the default network in AD and at-risk populations.
Articles from Behavioural Neurology are provided here courtesy of Wiley
Full text links
Read article at publisher's site: https://doi.org/10.3233/ben-2009-0231
Subscription required at IOSpress
http://iospress.metapress.com/openurl.asp?genre=article&issn=0953-4180&volume=21&issue=1&spage=77
Citations & impact
Impact metrics
Article citations
ApoE4 and Connectivity-Mediated Spreading of Tau Pathology at Lower Amyloid Levels.
JAMA Neurol, 80(12):1295-1306, 01 Dec 2023
Cited by: 8 articles | PMID: 37930695 | PMCID: PMC10628846
Women's Brain Health: Midlife Ovarian Removal Affects Associative Memory.
Mol Neurobiol, 60(11):6145-6159, 10 Jul 2023
Cited by: 1 article | PMID: 37423941 | PMCID: PMC10533588
Neuroimaging modalities in the detection of Alzheimer's disease-associated biomarkers.
Psychoradiology, 3:kkad009, 22 Jun 2023
Cited by: 2 articles | PMID: 38666112 | PMCID: PMC11003434
Review Free full text in Europe PMC
Novelty-Related fMRI Responses of Precuneus and Medial Temporal Regions in Individuals at Risk for Alzheimer Disease.
Neurology, 99(8):e775-e788, 03 Jun 2022
Cited by: 16 articles | PMID: 35995589 | PMCID: PMC9484732
Neuroimaging Modalities in Alzheimer's Disease: Diagnosis and Clinical Features.
Int J Mol Sci, 23(11):6079, 28 May 2022
Cited by: 18 articles | PMID: 35682758 | PMCID: PMC9181385
Review Free full text in Europe PMC
Go to all (62) article citations
Similar Articles
To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation.
Altered resting state networks in mild cognitive impairment and mild Alzheimer's disease: an fMRI study.
Hum Brain Mapp, 26(4):231-239, 01 Dec 2005
Cited by: 440 articles | PMID: 15954139 | PMCID: PMC6871685
Altered deactivation in individuals with genetic risk for Alzheimer's disease.
Neuropsychologia, 46(6):1679-1687, 14 Feb 2008
Cited by: 64 articles | PMID: 18346764
Evidence of altered posteromedial cortical FMRI activity in subjects at risk for Alzheimer disease.
Alzheimer Dis Assoc Disord, 24(1):28-36, 01 Jan 2010
Cited by: 44 articles | PMID: 19571734 | PMCID: PMC2837131
Functional alterations in memory networks in early Alzheimer's disease.
Neuromolecular Med, 12(1):27-43, 01 Mar 2010
Cited by: 330 articles | PMID: 20069392 | PMCID: PMC3036844
Review Free full text in Europe PMC
Funding
Funders who supported this work.
NIA NIH HHS (3)
Grant ID: P50-AG00513421
Grant ID: R01 AG027435
Grant ID: P01-AG04953
NINDS NIH HHS (1)
Grant ID: K23-NS02189