The Auditory Afferent Pathway as a Clinical Marker of Alzheimer's Disease.
- Publisher:
- IOS Press
- Publication Type:
- Journal Article
- Citation:
- J Alzheimers Dis, 2022, 85, (1), pp. 47-53
- Issue Date:
- 2022
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20274292_9994169270005671.pdf | 1.46 MB | Adobe PDF |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Shad, KF | |
dc.contributor.author | Soubra, W | |
dc.contributor.author | Cordato, DJ | |
dc.date.accessioned | 2023-02-14T23:52:30Z | |
dc.date.available | 2023-02-14T23:52:30Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | J Alzheimers Dis, 2022, 85, (1), pp. 47-53 | |
dc.identifier.issn | 1387-2877 | |
dc.identifier.issn | 1875-8908 | |
dc.identifier.uri | http://hdl.handle.net/10453/166122 | |
dc.description.abstract | Brain stem neural tracts and nuclei may be disturbed prior to observable neuronal atrophy in AD. In this perspective, we discuss the notion of functional deficits presenting prior to structural abnormalities in Alzheimer's disease (AD). Imaging of inferior colliculi using magnetic resonance spectroscopy (MRS) shows significant decrease in the neuronal markers, N acetyl aspartate/creatine ratio and increase in the glial marker myo-Inositol, in subjects with Mini-Mental State Examination scores greater than 24 and with no signs of atrophy in their MRI of the medial temporal lobe. Abnormalities in components of the auditory event-related potentials (ERPs) are described in cognitive impairment including AD. We observed a significant decrease in amplitude and increase in latency during the first 10 ms of auditory evoked potentials measured on electroencephalography (EEG) indicating slow auditory response of the brainstem. EEG spectral power recorded at the cortex is also associated with neural activity at the level of the inferior colliculi. We postulate that a functional examination of auditory afferent pathways, using non-invasive techniques, such as MRS, brain stem auditory evoked potentials (BAEPs) and ERPs may improve diagnostic accuracy of AD. Functional changes precede structural changes and it is important to further understand the relationship between biochemical and electrophysiological measures such as MRS, BAEPs and EEG. | |
dc.format | ||
dc.language | eng | |
dc.publisher | IOS Press | |
dc.relation.ispartof | J Alzheimers Dis | |
dc.relation.isbasedon | 10.3233/JAD-215206 | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 1103 Clinical Sciences, 1109 Neurosciences, 1702 Cognitive Sciences | |
dc.subject.classification | Neurology & Neurosurgery | |
dc.subject.mesh | Acoustic Stimulation | |
dc.subject.mesh | Afferent Pathways | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Alzheimer Disease | |
dc.subject.mesh | Aspartic Acid | |
dc.subject.mesh | Biomarkers | |
dc.subject.mesh | Cerebral Cortex | |
dc.subject.mesh | Cognitive Dysfunction | |
dc.subject.mesh | Creatine | |
dc.subject.mesh | Electroencephalography | |
dc.subject.mesh | Evoked Potentials, Auditory | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Inositol | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Magnetic Resonance Spectroscopy | |
dc.subject.mesh | Male | |
dc.subject.mesh | Mental Status and Dementia Tests | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Temporal Lobe | |
dc.subject.mesh | Cerebral Cortex | |
dc.subject.mesh | Temporal Lobe | |
dc.subject.mesh | Afferent Pathways | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Alzheimer Disease | |
dc.subject.mesh | Inositol | |
dc.subject.mesh | Creatine | |
dc.subject.mesh | Aspartic Acid | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Electroencephalography | |
dc.subject.mesh | Acoustic Stimulation | |
dc.subject.mesh | Magnetic Resonance Spectroscopy | |
dc.subject.mesh | Evoked Potentials, Auditory | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Female | |
dc.subject.mesh | Male | |
dc.subject.mesh | Biomarkers | |
dc.subject.mesh | Cognitive Dysfunction | |
dc.subject.mesh | Mental Status and Dementia Tests | |
dc.title | The Auditory Afferent Pathway as a Clinical Marker of Alzheimer's Disease. | |
dc.type | Journal Article | |
utslib.citation.volume | 85 | |
utslib.location.activity | Netherlands | |
utslib.for | 1103 Clinical Sciences | |
utslib.for | 1109 Neurosciences | |
utslib.for | 1702 Cognitive Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
utslib.copyright.status | closed_access | * |
dc.date.updated | 2023-02-14T23:52:28Z | |
pubs.issue | 1 | |
pubs.publication-status | Published | |
pubs.volume | 85 | |
utslib.citation.issue | 1 |
Abstract:
Brain stem neural tracts and nuclei may be disturbed prior to observable neuronal atrophy in AD. In this perspective, we discuss the notion of functional deficits presenting prior to structural abnormalities in Alzheimer's disease (AD). Imaging of inferior colliculi using magnetic resonance spectroscopy (MRS) shows significant decrease in the neuronal markers, N acetyl aspartate/creatine ratio and increase in the glial marker myo-Inositol, in subjects with Mini-Mental State Examination scores greater than 24 and with no signs of atrophy in their MRI of the medial temporal lobe. Abnormalities in components of the auditory event-related potentials (ERPs) are described in cognitive impairment including AD. We observed a significant decrease in amplitude and increase in latency during the first 10 ms of auditory evoked potentials measured on electroencephalography (EEG) indicating slow auditory response of the brainstem. EEG spectral power recorded at the cortex is also associated with neural activity at the level of the inferior colliculi. We postulate that a functional examination of auditory afferent pathways, using non-invasive techniques, such as MRS, brain stem auditory evoked potentials (BAEPs) and ERPs may improve diagnostic accuracy of AD. Functional changes precede structural changes and it is important to further understand the relationship between biochemical and electrophysiological measures such as MRS, BAEPs and EEG.
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