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Hypomania, Depression, Euthymia: New Evidence in Parkinson's Disease

The field related to mood disorders in Parkinson's disease (PD) is fragmented. The aim of this cohort observational study was to evaluate whether the episodes of mood alteration could appear in different disease stages and to verify how nonmotor symptoms were led off into different stages. We e...

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Autores principales: Canesi, Margherita, Lavolpe, Sara, Cereda, Viviana, Ranghetti, Alessandra, Maestri, Roberto, Pezzoli, Gianni, Rusconi, Maria Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718041/
https://www.ncbi.nlm.nih.gov/pubmed/33294055
http://dx.doi.org/10.1155/2020/5139237
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author Canesi, Margherita
Lavolpe, Sara
Cereda, Viviana
Ranghetti, Alessandra
Maestri, Roberto
Pezzoli, Gianni
Rusconi, Maria Luisa
author_facet Canesi, Margherita
Lavolpe, Sara
Cereda, Viviana
Ranghetti, Alessandra
Maestri, Roberto
Pezzoli, Gianni
Rusconi, Maria Luisa
author_sort Canesi, Margherita
collection PubMed
description The field related to mood disorders in Parkinson's disease (PD) is fragmented. The aim of this cohort observational study was to evaluate whether the episodes of mood alteration could appear in different disease stages and to verify how nonmotor symptoms were led off into different stages. We enrolled 93 PD outpatients (three groups: drug naive—DN; not exhibiting motor fluctuations—n-MF; and exhibiting motor fluctuations—MF) and 50 healthy controls. Mood state was assessed through the Internal State Scale (ISS) while depressive symptoms were evaluated through the Beck Depression Inventory-II (BDI-II), nonmotor symptoms by means of the Non-Motor Symptoms Scale (NMSS), and the presence of impulse control disorders (ICDs) with the Questionnaire for Impulsive-Compulsive Disorders in Parkinson's Disease (QUIP). Clinical and pharmacological data have also been recorded. No significant differences in mood state distribution between groups were observed. Nevertheless, as regards the mood state distribution within groups, in n-MF (47.6%) and MF patients (50%), (hypo)mania presence was significantly higher than other symptoms. In DN patients, hypomania showed a prevalence of 38.1% although it was not significant. At least one ICD was reported in 29.3% of n-MF and 50% of MF patients. In the MF group, a moderate positive correlation between ISS ACTivation subscale scores and the presence of ICDs and compulsive medication use emerged. Finally, MF patients reported higher BDI-II total scores than DN. Our results show that mood alterations in PD, considering both depressive symptoms and mood elevation, are related to the advanced stages of the disease as well as the presence of ICDs, and dopaminergic therapy would not always be able to restore a normal mood condition.
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spelling pubmed-77180412020-12-07 Hypomania, Depression, Euthymia: New Evidence in Parkinson's Disease Canesi, Margherita Lavolpe, Sara Cereda, Viviana Ranghetti, Alessandra Maestri, Roberto Pezzoli, Gianni Rusconi, Maria Luisa Behav Neurol Research Article The field related to mood disorders in Parkinson's disease (PD) is fragmented. The aim of this cohort observational study was to evaluate whether the episodes of mood alteration could appear in different disease stages and to verify how nonmotor symptoms were led off into different stages. We enrolled 93 PD outpatients (three groups: drug naive—DN; not exhibiting motor fluctuations—n-MF; and exhibiting motor fluctuations—MF) and 50 healthy controls. Mood state was assessed through the Internal State Scale (ISS) while depressive symptoms were evaluated through the Beck Depression Inventory-II (BDI-II), nonmotor symptoms by means of the Non-Motor Symptoms Scale (NMSS), and the presence of impulse control disorders (ICDs) with the Questionnaire for Impulsive-Compulsive Disorders in Parkinson's Disease (QUIP). Clinical and pharmacological data have also been recorded. No significant differences in mood state distribution between groups were observed. Nevertheless, as regards the mood state distribution within groups, in n-MF (47.6%) and MF patients (50%), (hypo)mania presence was significantly higher than other symptoms. In DN patients, hypomania showed a prevalence of 38.1% although it was not significant. At least one ICD was reported in 29.3% of n-MF and 50% of MF patients. In the MF group, a moderate positive correlation between ISS ACTivation subscale scores and the presence of ICDs and compulsive medication use emerged. Finally, MF patients reported higher BDI-II total scores than DN. Our results show that mood alterations in PD, considering both depressive symptoms and mood elevation, are related to the advanced stages of the disease as well as the presence of ICDs, and dopaminergic therapy would not always be able to restore a normal mood condition. Hindawi 2020-11-26 /pmc/articles/PMC7718041/ /pubmed/33294055 http://dx.doi.org/10.1155/2020/5139237 Text en Copyright © 2020 Margherita Canesi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Canesi, Margherita
Lavolpe, Sara
Cereda, Viviana
Ranghetti, Alessandra
Maestri, Roberto
Pezzoli, Gianni
Rusconi, Maria Luisa
Hypomania, Depression, Euthymia: New Evidence in Parkinson's Disease
title Hypomania, Depression, Euthymia: New Evidence in Parkinson's Disease
title_full Hypomania, Depression, Euthymia: New Evidence in Parkinson's Disease
title_fullStr Hypomania, Depression, Euthymia: New Evidence in Parkinson's Disease
title_full_unstemmed Hypomania, Depression, Euthymia: New Evidence in Parkinson's Disease
title_short Hypomania, Depression, Euthymia: New Evidence in Parkinson's Disease
title_sort hypomania, depression, euthymia: new evidence in parkinson's disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718041/
https://www.ncbi.nlm.nih.gov/pubmed/33294055
http://dx.doi.org/10.1155/2020/5139237
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