Cargando…

Single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe

OBJECTIVE: Impaired memory is a common comorbidity of refractory temporal lobe epilepsy (TLE) and often perceived by patients as more problematic than the seizures themselves. The objective of this study is to understand what the relationship of these behavioral impairments is to the underlying path...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Seung J., Beam, Danielle E., Schjetnan, Andrea G. P., Paul, Lynn K., Chandravadia, Nand, Reed, Chrystal M., Chung, Jeffrey M., Ross, Ian B., Valiante, Taufik A., Mamelak, Adam N., Rutishauser, Ueli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403636/
https://www.ncbi.nlm.nih.gov/pubmed/34289113
http://dx.doi.org/10.1111/epi.17010
_version_ 1783746031852191744
author Lee, Seung J.
Beam, Danielle E.
Schjetnan, Andrea G. P.
Paul, Lynn K.
Chandravadia, Nand
Reed, Chrystal M.
Chung, Jeffrey M.
Ross, Ian B.
Valiante, Taufik A.
Mamelak, Adam N.
Rutishauser, Ueli
author_facet Lee, Seung J.
Beam, Danielle E.
Schjetnan, Andrea G. P.
Paul, Lynn K.
Chandravadia, Nand
Reed, Chrystal M.
Chung, Jeffrey M.
Ross, Ian B.
Valiante, Taufik A.
Mamelak, Adam N.
Rutishauser, Ueli
author_sort Lee, Seung J.
collection PubMed
description OBJECTIVE: Impaired memory is a common comorbidity of refractory temporal lobe epilepsy (TLE) and often perceived by patients as more problematic than the seizures themselves. The objective of this study is to understand what the relationship of these behavioral impairments is to the underlying pathophysiology, as there are currently no treatments for these deficits, and it remains unknown what circuits are affected. METHODS: We recorded single neurons in the medial temporal lobes (MTLs) of 62 patients (37 with refractory TLE) who performed a visual recognition memory task to characterize the relationship between behavior, tuning, and anatomical location of memory selective and visually selective neurons. RESULTS: Subjects with a seizure onset zone (SOZ) in the right but not left MTL demonstrated impaired ability to recollect as indicated by the degree of asymmetry of the receiver operating characteristic curve. Of the 1973 recorded neurons, 159 were memory selective (MS) and 366 were visually selective (VS) category cells. The responses of MS neurons located within right but not left MTL SOZs were impaired during high‐confidence retrieval trials, mirroring the behavioral deficit seen both in our task and in standardized neuropsychological tests. In contrast, responses of VS neurons were unimpaired in both left and right MTL SOZs. Our findings show that neuronal dysfunction within SOZs in the MTL was specific to a functional cell type and behavior, whereas other cell types respond normally even within the SOZ. We show behavioral metrics that detect right MTL SOZ‐related deficits and identify a neuronal correlate of this impairment. SIGNIFICANCE: Together, these findings show that single‐cell responses can be used to assess the causal effects of local circuit disruption by an SOZ in the MTL, and establish a neural correlate of cognitive impairment due to epilepsy that can be used as a biomarker to assess the efficacy of novel treatments.
format Online
Article
Text
id pubmed-8403636
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-84036362021-09-27 Single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe Lee, Seung J. Beam, Danielle E. Schjetnan, Andrea G. P. Paul, Lynn K. Chandravadia, Nand Reed, Chrystal M. Chung, Jeffrey M. Ross, Ian B. Valiante, Taufik A. Mamelak, Adam N. Rutishauser, Ueli Epilepsia Full‐length Original Research OBJECTIVE: Impaired memory is a common comorbidity of refractory temporal lobe epilepsy (TLE) and often perceived by patients as more problematic than the seizures themselves. The objective of this study is to understand what the relationship of these behavioral impairments is to the underlying pathophysiology, as there are currently no treatments for these deficits, and it remains unknown what circuits are affected. METHODS: We recorded single neurons in the medial temporal lobes (MTLs) of 62 patients (37 with refractory TLE) who performed a visual recognition memory task to characterize the relationship between behavior, tuning, and anatomical location of memory selective and visually selective neurons. RESULTS: Subjects with a seizure onset zone (SOZ) in the right but not left MTL demonstrated impaired ability to recollect as indicated by the degree of asymmetry of the receiver operating characteristic curve. Of the 1973 recorded neurons, 159 were memory selective (MS) and 366 were visually selective (VS) category cells. The responses of MS neurons located within right but not left MTL SOZs were impaired during high‐confidence retrieval trials, mirroring the behavioral deficit seen both in our task and in standardized neuropsychological tests. In contrast, responses of VS neurons were unimpaired in both left and right MTL SOZs. Our findings show that neuronal dysfunction within SOZs in the MTL was specific to a functional cell type and behavior, whereas other cell types respond normally even within the SOZ. We show behavioral metrics that detect right MTL SOZ‐related deficits and identify a neuronal correlate of this impairment. SIGNIFICANCE: Together, these findings show that single‐cell responses can be used to assess the causal effects of local circuit disruption by an SOZ in the MTL, and establish a neural correlate of cognitive impairment due to epilepsy that can be used as a biomarker to assess the efficacy of novel treatments. John Wiley and Sons Inc. 2021-07-21 2021-09 /pmc/articles/PMC8403636/ /pubmed/34289113 http://dx.doi.org/10.1111/epi.17010 Text en © 2021 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full‐length Original Research
Lee, Seung J.
Beam, Danielle E.
Schjetnan, Andrea G. P.
Paul, Lynn K.
Chandravadia, Nand
Reed, Chrystal M.
Chung, Jeffrey M.
Ross, Ian B.
Valiante, Taufik A.
Mamelak, Adam N.
Rutishauser, Ueli
Single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe
title Single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe
title_full Single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe
title_fullStr Single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe
title_full_unstemmed Single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe
title_short Single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe
title_sort single‐neuron correlate of epilepsy‐related cognitive deficits in visual recognition memory in right mesial temporal lobe
topic Full‐length Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403636/
https://www.ncbi.nlm.nih.gov/pubmed/34289113
http://dx.doi.org/10.1111/epi.17010
work_keys_str_mv AT leeseungj singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT beamdaniellee singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT schjetnanandreagp singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT paullynnk singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT chandravadianand singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT reedchrystalm singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT chungjeffreym singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT rossianb singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT valiantetaufika singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT mamelakadamn singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe
AT rutishauserueli singleneuroncorrelateofepilepsyrelatedcognitivedeficitsinvisualrecognitionmemoryinrightmesialtemporallobe