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Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer's disease spectrum

BACKGROUND: Alzheimer's disease (AD) is generally thought to spare primary sensory function; however, such interpretations have drawn from a literature that has rarely taken into account the variable cognitive declines seen in patients with AD. As these cognitive domains are now known to modula...

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Autores principales: Wiesman, Alex I., Mundorf, Victoria M., Casagrande, Chloe C., Wolfson, Sara L., Johnson, Craig M., May, Pamela E., Murman, Daniel L., Wilson, Tony W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550984/
https://www.ncbi.nlm.nih.gov/pubmed/34689085
http://dx.doi.org/10.1016/j.ebiom.2021.103638
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author Wiesman, Alex I.
Mundorf, Victoria M.
Casagrande, Chloe C.
Wolfson, Sara L.
Johnson, Craig M.
May, Pamela E.
Murman, Daniel L.
Wilson, Tony W.
author_facet Wiesman, Alex I.
Mundorf, Victoria M.
Casagrande, Chloe C.
Wolfson, Sara L.
Johnson, Craig M.
May, Pamela E.
Murman, Daniel L.
Wilson, Tony W.
author_sort Wiesman, Alex I.
collection PubMed
description BACKGROUND: Alzheimer's disease (AD) is generally thought to spare primary sensory function; however, such interpretations have drawn from a literature that has rarely taken into account the variable cognitive declines seen in patients with AD. As these cognitive domains are now known to modulate cortical somatosensory processing, it remains possible that abnormalities in somatosensory function in patients with AD have been suppressed by neuropsychological variability in previous research. METHODS: In this study, we combine magnetoencephalographic (MEG) brain imaging during a paired-pulse somatosensory gating task with an extensive battery of neuropsychological tests to investigate the influence of cognitive variability on estimated differences in somatosensory function between biomarker-confirmed patients on the AD spectrum and cognitively-normal older adults. FINDINGS: We show that patients on the AD spectrum exhibit largely non-significant differences in somatosensory function when cognitive variability is not considered (p-value range: .020–.842). However, once attention and processing speed abilities are considered, robust differences in gamma-frequency somatosensory response amplitude (p < .001) and gating (p = .004) emerge, accompanied by significant statistical suppression effects. INTERPRETATION: These findings suggest that patients with AD exhibit insults to functional somatosensory processing in primary sensory cortices, but these effects are masked by variability in cognitive decline across individuals. FUNDING: National Institutes of Health, USA; Fremont Area Alzheimer's Fund, USA
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spelling pubmed-85509842021-11-04 Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer's disease spectrum Wiesman, Alex I. Mundorf, Victoria M. Casagrande, Chloe C. Wolfson, Sara L. Johnson, Craig M. May, Pamela E. Murman, Daniel L. Wilson, Tony W. EBioMedicine Research paper BACKGROUND: Alzheimer's disease (AD) is generally thought to spare primary sensory function; however, such interpretations have drawn from a literature that has rarely taken into account the variable cognitive declines seen in patients with AD. As these cognitive domains are now known to modulate cortical somatosensory processing, it remains possible that abnormalities in somatosensory function in patients with AD have been suppressed by neuropsychological variability in previous research. METHODS: In this study, we combine magnetoencephalographic (MEG) brain imaging during a paired-pulse somatosensory gating task with an extensive battery of neuropsychological tests to investigate the influence of cognitive variability on estimated differences in somatosensory function between biomarker-confirmed patients on the AD spectrum and cognitively-normal older adults. FINDINGS: We show that patients on the AD spectrum exhibit largely non-significant differences in somatosensory function when cognitive variability is not considered (p-value range: .020–.842). However, once attention and processing speed abilities are considered, robust differences in gamma-frequency somatosensory response amplitude (p < .001) and gating (p = .004) emerge, accompanied by significant statistical suppression effects. INTERPRETATION: These findings suggest that patients with AD exhibit insults to functional somatosensory processing in primary sensory cortices, but these effects are masked by variability in cognitive decline across individuals. FUNDING: National Institutes of Health, USA; Fremont Area Alzheimer's Fund, USA Elsevier 2021-10-21 /pmc/articles/PMC8550984/ /pubmed/34689085 http://dx.doi.org/10.1016/j.ebiom.2021.103638 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research paper
Wiesman, Alex I.
Mundorf, Victoria M.
Casagrande, Chloe C.
Wolfson, Sara L.
Johnson, Craig M.
May, Pamela E.
Murman, Daniel L.
Wilson, Tony W.
Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer's disease spectrum
title Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer's disease spectrum
title_full Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer's disease spectrum
title_fullStr Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer's disease spectrum
title_full_unstemmed Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer's disease spectrum
title_short Somatosensory dysfunction is masked by variable cognitive deficits across patients on the Alzheimer's disease spectrum
title_sort somatosensory dysfunction is masked by variable cognitive deficits across patients on the alzheimer's disease spectrum
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550984/
https://www.ncbi.nlm.nih.gov/pubmed/34689085
http://dx.doi.org/10.1016/j.ebiom.2021.103638
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