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Cortical Inhibition and Plasticity in Major Depressive Disorder

BACKGROUND: Major depressive disorder (MDD) is a severe psychiatric disorder that is associated with various cognitive impairments, including learning and memory deficits. As synaptic plasticity is considered an important mechanism underlying learning and memory, deficits in cortical plasticity migh...

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Autores principales: Castricum, Jesminne, Birkenhager, Tom K., Kushner, Steven A., Elgersma, Ype, Tulen, Joke H. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825489/
https://www.ncbi.nlm.nih.gov/pubmed/35153873
http://dx.doi.org/10.3389/fpsyt.2022.777422
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author Castricum, Jesminne
Birkenhager, Tom K.
Kushner, Steven A.
Elgersma, Ype
Tulen, Joke H. M.
author_facet Castricum, Jesminne
Birkenhager, Tom K.
Kushner, Steven A.
Elgersma, Ype
Tulen, Joke H. M.
author_sort Castricum, Jesminne
collection PubMed
description BACKGROUND: Major depressive disorder (MDD) is a severe psychiatric disorder that is associated with various cognitive impairments, including learning and memory deficits. As synaptic plasticity is considered an important mechanism underlying learning and memory, deficits in cortical plasticity might play a role in the pathophysiology of patients with MDD. We used Transcranial Magnetic Stimulation (TMS) to assess inhibitory neurotransmission and cortical plasticity in the motor cortex of MDD patients and controls. METHODS: We measured the cortical silent period (CSP) and short interval cortical inhibition (SICI), as well as intermittent theta-burst stimulation (iTBS), in 9 drug-free MDD inpatients and 18 controls. RESULTS: The overall response to the CSP, SICI, and iTBS paradigms was not significantly different between the patient and control groups. iTBS induction resulted in significant potentiation after 20 mins in the control group (t((17)) = −2.8, p = 0.01), whereas no potentiation was observed in patients. CONCLUSIONS: Potentiation of MEP amplitudes was not observed within the MDD group. No evidence was found for medium-to-large effect size differences in CSP and SICI measures in severely depressed drug-free patients, suggesting that reduced cortical inhibition is unlikely to be a robust correlate of the pathophysiological mechanism in MDD. However, these findings should be interpreted with caution due to the high inter-subject variability and the small sample size. SIGNIFICANCE: These findings advance our understanding of neurophysiological functioning in drug-free severely depressed inpatients.
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spelling pubmed-88254892022-02-10 Cortical Inhibition and Plasticity in Major Depressive Disorder Castricum, Jesminne Birkenhager, Tom K. Kushner, Steven A. Elgersma, Ype Tulen, Joke H. M. Front Psychiatry Psychiatry BACKGROUND: Major depressive disorder (MDD) is a severe psychiatric disorder that is associated with various cognitive impairments, including learning and memory deficits. As synaptic plasticity is considered an important mechanism underlying learning and memory, deficits in cortical plasticity might play a role in the pathophysiology of patients with MDD. We used Transcranial Magnetic Stimulation (TMS) to assess inhibitory neurotransmission and cortical plasticity in the motor cortex of MDD patients and controls. METHODS: We measured the cortical silent period (CSP) and short interval cortical inhibition (SICI), as well as intermittent theta-burst stimulation (iTBS), in 9 drug-free MDD inpatients and 18 controls. RESULTS: The overall response to the CSP, SICI, and iTBS paradigms was not significantly different between the patient and control groups. iTBS induction resulted in significant potentiation after 20 mins in the control group (t((17)) = −2.8, p = 0.01), whereas no potentiation was observed in patients. CONCLUSIONS: Potentiation of MEP amplitudes was not observed within the MDD group. No evidence was found for medium-to-large effect size differences in CSP and SICI measures in severely depressed drug-free patients, suggesting that reduced cortical inhibition is unlikely to be a robust correlate of the pathophysiological mechanism in MDD. However, these findings should be interpreted with caution due to the high inter-subject variability and the small sample size. SIGNIFICANCE: These findings advance our understanding of neurophysiological functioning in drug-free severely depressed inpatients. Frontiers Media S.A. 2022-01-26 /pmc/articles/PMC8825489/ /pubmed/35153873 http://dx.doi.org/10.3389/fpsyt.2022.777422 Text en Copyright © 2022 Castricum, Birkenhager, Kushner, Elgersma and Tulen. 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 Psychiatry
Castricum, Jesminne
Birkenhager, Tom K.
Kushner, Steven A.
Elgersma, Ype
Tulen, Joke H. M.
Cortical Inhibition and Plasticity in Major Depressive Disorder
title Cortical Inhibition and Plasticity in Major Depressive Disorder
title_full Cortical Inhibition and Plasticity in Major Depressive Disorder
title_fullStr Cortical Inhibition and Plasticity in Major Depressive Disorder
title_full_unstemmed Cortical Inhibition and Plasticity in Major Depressive Disorder
title_short Cortical Inhibition and Plasticity in Major Depressive Disorder
title_sort cortical inhibition and plasticity in major depressive disorder
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825489/
https://www.ncbi.nlm.nih.gov/pubmed/35153873
http://dx.doi.org/10.3389/fpsyt.2022.777422
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