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Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment
Depression is one of the most frequent and burdensome non-motor symptoms in Parkinson’s disease (PD), across all stages. Even when its severity is mild, PD depression has a great impact on quality of life for these patients and their caregivers. Accordingly, accurate diagnosis, supported by validate...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200562/ https://www.ncbi.nlm.nih.gov/pubmed/35705848 http://dx.doi.org/10.1007/s40266-022-00942-1 |
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author | Prange, Stéphane Klinger, Hélène Laurencin, Chloé Danaila, Teodor Thobois, Stéphane |
author_facet | Prange, Stéphane Klinger, Hélène Laurencin, Chloé Danaila, Teodor Thobois, Stéphane |
author_sort | Prange, Stéphane |
collection | PubMed |
description | Depression is one of the most frequent and burdensome non-motor symptoms in Parkinson’s disease (PD), across all stages. Even when its severity is mild, PD depression has a great impact on quality of life for these patients and their caregivers. Accordingly, accurate diagnosis, supported by validated scales, identification of risk factors, and recognition of motor and non-motor symptoms comorbid to depression are critical to understanding the neurobiology of depression, which in turn determines the effectiveness of dopaminergic drugs, antidepressants and non-pharmacological interventions. Recent advances using in vivo functional and structural imaging demonstrate that PD depression is underpinned by dysfunction of limbic networks and monoaminergic systems, depending on the stage of PD and its associated symptoms, including apathy, anxiety, rapid eye movement sleep behavior disorder (RBD), cognitive impairment and dementia. In particular, the evolution of serotonergic, noradrenergic, and dopaminergic dysfunction and abnormalities of limbic circuits across time, involving the anterior cingulate and orbitofrontal cortices, amygdala, thalamus and ventral striatum, help to delineate the variable expression of depression in patients with prodromal, early and advanced PD. Evidence is accumulating to support the use of dual serotonin and noradrenaline reuptake inhibitors (desipramine, nortriptyline, venlafaxine) in patients with PD and moderate to severe depression, while selective serotonin reuptake inhibitors, repetitive transcranial magnetic stimulation and cognitive behavioral therapy may also be considered. In all patients, recent findings advocate that optimization of dopamine replacement therapy and evaluation of deep brain stimulation of the subthalamic nucleus to improve motor symptoms represents an important first step, in addition to physical activity. Overall, this review indicates that increasing understanding of neurobiological changes help to implement a roadmap of tailored interventions for patients with PD and depression, depending on the stage and comorbid symptoms underlying PD subtypes and their prognosis. |
format | Online Article Text |
id | pubmed-9200562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-92005622022-06-17 Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment Prange, Stéphane Klinger, Hélène Laurencin, Chloé Danaila, Teodor Thobois, Stéphane Drugs Aging Review Article Depression is one of the most frequent and burdensome non-motor symptoms in Parkinson’s disease (PD), across all stages. Even when its severity is mild, PD depression has a great impact on quality of life for these patients and their caregivers. Accordingly, accurate diagnosis, supported by validated scales, identification of risk factors, and recognition of motor and non-motor symptoms comorbid to depression are critical to understanding the neurobiology of depression, which in turn determines the effectiveness of dopaminergic drugs, antidepressants and non-pharmacological interventions. Recent advances using in vivo functional and structural imaging demonstrate that PD depression is underpinned by dysfunction of limbic networks and monoaminergic systems, depending on the stage of PD and its associated symptoms, including apathy, anxiety, rapid eye movement sleep behavior disorder (RBD), cognitive impairment and dementia. In particular, the evolution of serotonergic, noradrenergic, and dopaminergic dysfunction and abnormalities of limbic circuits across time, involving the anterior cingulate and orbitofrontal cortices, amygdala, thalamus and ventral striatum, help to delineate the variable expression of depression in patients with prodromal, early and advanced PD. Evidence is accumulating to support the use of dual serotonin and noradrenaline reuptake inhibitors (desipramine, nortriptyline, venlafaxine) in patients with PD and moderate to severe depression, while selective serotonin reuptake inhibitors, repetitive transcranial magnetic stimulation and cognitive behavioral therapy may also be considered. In all patients, recent findings advocate that optimization of dopamine replacement therapy and evaluation of deep brain stimulation of the subthalamic nucleus to improve motor symptoms represents an important first step, in addition to physical activity. Overall, this review indicates that increasing understanding of neurobiological changes help to implement a roadmap of tailored interventions for patients with PD and depression, depending on the stage and comorbid symptoms underlying PD subtypes and their prognosis. Springer International Publishing 2022-06-16 2022 /pmc/articles/PMC9200562/ /pubmed/35705848 http://dx.doi.org/10.1007/s40266-022-00942-1 Text en © The Author(s) 2022, Corrected Publication 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Review Article Prange, Stéphane Klinger, Hélène Laurencin, Chloé Danaila, Teodor Thobois, Stéphane Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment |
title | Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment |
title_full | Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment |
title_fullStr | Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment |
title_full_unstemmed | Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment |
title_short | Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment |
title_sort | depression in patients with parkinson’s disease: current understanding of its neurobiology and implications for treatment |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200562/ https://www.ncbi.nlm.nih.gov/pubmed/35705848 http://dx.doi.org/10.1007/s40266-022-00942-1 |
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