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Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS
Pseudobulbar affect is a disorder of emotional expression commonly observed in amyotrophic lateral sclerosis (ALS), presenting as episodes of involuntary laughter, or crying. The objective of the current study was to determine the association between frequency of pathological laughter and crying (PL...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296641/ https://www.ncbi.nlm.nih.gov/pubmed/34305804 http://dx.doi.org/10.3389/fneur.2021.704059 |
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author | Tu, Sicong Huang, Mengjie Caga, Jashelle Mahoney, Colin J. Kiernan, Matthew C. |
author_facet | Tu, Sicong Huang, Mengjie Caga, Jashelle Mahoney, Colin J. Kiernan, Matthew C. |
author_sort | Tu, Sicong |
collection | PubMed |
description | Pseudobulbar affect is a disorder of emotional expression commonly observed in amyotrophic lateral sclerosis (ALS), presenting as episodes of involuntary laughter, or crying. The objective of the current study was to determine the association between frequency of pathological laughter and crying (PLC) episodes with clinical features, cognitive impairment, and brainstem pathology. Thirty-five sporadic ALS patients underwent neuropsychological assessment, with a subset also undergoing brain imaging. The Center for Neurological Study Lability Scale (CNS-LS) was used to screen for presence and severity of pseudobulbar affect (CNS-LS ≥ 13) and frequency of PLC episodes. Presence of pseudobulbar affect was significantly higher in bulbar onset ALS (p = 0.02). Frequency of PLC episodes was differentially associated with cognitive performance and brainstem integrity. Notably pathological laughter frequency, but not crying, showed a significant positive association with executive dysfunction on the Trail Making Test B-A (R(2) = 0.14, p = 0.04). Similarly, only pathological laughter frequency demonstrated a significant negative correlation with gray matter volume of the brainstem (R(2) = 0.46, p < 0.01), and mean fractional anisotropy of the superior cerebellar peduncles (left: R(2) = 0.44, p < 0.01; right: R(2) = 0.44, p < 0.01). Hierarchical regression indicated brainstem imaging in combination with site of symptom onset explained 73% of the variance in pathological laughter frequency in ALS. The current findings suggest emotional lability is underpinned by degeneration across distinct neural circuits, with brainstem integrity critical in the emergence of pathological laughter. |
format | Online Article Text |
id | pubmed-8296641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82966412021-07-23 Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS Tu, Sicong Huang, Mengjie Caga, Jashelle Mahoney, Colin J. Kiernan, Matthew C. Front Neurol Neurology Pseudobulbar affect is a disorder of emotional expression commonly observed in amyotrophic lateral sclerosis (ALS), presenting as episodes of involuntary laughter, or crying. The objective of the current study was to determine the association between frequency of pathological laughter and crying (PLC) episodes with clinical features, cognitive impairment, and brainstem pathology. Thirty-five sporadic ALS patients underwent neuropsychological assessment, with a subset also undergoing brain imaging. The Center for Neurological Study Lability Scale (CNS-LS) was used to screen for presence and severity of pseudobulbar affect (CNS-LS ≥ 13) and frequency of PLC episodes. Presence of pseudobulbar affect was significantly higher in bulbar onset ALS (p = 0.02). Frequency of PLC episodes was differentially associated with cognitive performance and brainstem integrity. Notably pathological laughter frequency, but not crying, showed a significant positive association with executive dysfunction on the Trail Making Test B-A (R(2) = 0.14, p = 0.04). Similarly, only pathological laughter frequency demonstrated a significant negative correlation with gray matter volume of the brainstem (R(2) = 0.46, p < 0.01), and mean fractional anisotropy of the superior cerebellar peduncles (left: R(2) = 0.44, p < 0.01; right: R(2) = 0.44, p < 0.01). Hierarchical regression indicated brainstem imaging in combination with site of symptom onset explained 73% of the variance in pathological laughter frequency in ALS. The current findings suggest emotional lability is underpinned by degeneration across distinct neural circuits, with brainstem integrity critical in the emergence of pathological laughter. Frontiers Media S.A. 2021-07-08 /pmc/articles/PMC8296641/ /pubmed/34305804 http://dx.doi.org/10.3389/fneur.2021.704059 Text en Copyright © 2021 Tu, Huang, Caga, Mahoney and Kiernan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Tu, Sicong Huang, Mengjie Caga, Jashelle Mahoney, Colin J. Kiernan, Matthew C. Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS |
title | Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS |
title_full | Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS |
title_fullStr | Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS |
title_full_unstemmed | Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS |
title_short | Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS |
title_sort | brainstem correlates of pathological laughter and crying frequency in als |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296641/ https://www.ncbi.nlm.nih.gov/pubmed/34305804 http://dx.doi.org/10.3389/fneur.2021.704059 |
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