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Late life bipolar disorder evolving into frontotemporal dementia mimic

OBJECTIVES: Although bipolar disorder has been understood classically as a cyclic disease with full recovery between mood episodes, in the last decade, evidence has accumulated supporting progressive features. The clinical picture of advanced or end-stage bipolar disorder is heterogeneous with possi...

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Autores principales: Dols, Annemiek, Krudop, Welmoed, Möller, Christiane, Shulman, Kenneth, Sajatovic, Martha, Pijnenburg, Yolande AL
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019473/
https://www.ncbi.nlm.nih.gov/pubmed/27660450
http://dx.doi.org/10.2147/NDT.S99229
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author Dols, Annemiek
Krudop, Welmoed
Möller, Christiane
Shulman, Kenneth
Sajatovic, Martha
Pijnenburg, Yolande AL
author_facet Dols, Annemiek
Krudop, Welmoed
Möller, Christiane
Shulman, Kenneth
Sajatovic, Martha
Pijnenburg, Yolande AL
author_sort Dols, Annemiek
collection PubMed
description OBJECTIVES: Although bipolar disorder has been understood classically as a cyclic disease with full recovery between mood episodes, in the last decade, evidence has accumulated supporting progressive features. The clinical picture of advanced or end-stage bipolar disorder is heterogeneous with possible deficits in cognition and behavior, as illustrated by our case series. CASES: From our neuropsychiatric outpatient clinic, we describe four cases with bipolar disorder gradually developing a clinical syndrome, including apathy, disinhibition, loss of empathy, stereotypical behavior, and compulsiveness, fulfilling the criteria for possible behavioral variant frontotemporal dementia. All cases were diagnosed with bipolar 1 disorder at least 10 years before the onset of the current symptoms, which were not due to recent mood episodes or switches of medication. In all cases, 3–7 years of follow-up yielded no progression. Repeated neuroimaging was within normal limits. Cerebrospinal fluid biomarker studies were not supportive of underlying neurodegenerative pathology. C9orf72 mutation status was negative in all cases. CONCLUSION: Symptoms fitting the criteria for possible behavioral variant frontotemporal dementia may be present in end-stage of bipolar disorder. An alternative neurodegenerative nature seems unlikely based on repeated normal neuroimaging and the absence of clinical progression. Functional involvement of the frontal-subcortical networks might play a role.
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spelling pubmed-50194732016-09-22 Late life bipolar disorder evolving into frontotemporal dementia mimic Dols, Annemiek Krudop, Welmoed Möller, Christiane Shulman, Kenneth Sajatovic, Martha Pijnenburg, Yolande AL Neuropsychiatr Dis Treat Case Series OBJECTIVES: Although bipolar disorder has been understood classically as a cyclic disease with full recovery between mood episodes, in the last decade, evidence has accumulated supporting progressive features. The clinical picture of advanced or end-stage bipolar disorder is heterogeneous with possible deficits in cognition and behavior, as illustrated by our case series. CASES: From our neuropsychiatric outpatient clinic, we describe four cases with bipolar disorder gradually developing a clinical syndrome, including apathy, disinhibition, loss of empathy, stereotypical behavior, and compulsiveness, fulfilling the criteria for possible behavioral variant frontotemporal dementia. All cases were diagnosed with bipolar 1 disorder at least 10 years before the onset of the current symptoms, which were not due to recent mood episodes or switches of medication. In all cases, 3–7 years of follow-up yielded no progression. Repeated neuroimaging was within normal limits. Cerebrospinal fluid biomarker studies were not supportive of underlying neurodegenerative pathology. C9orf72 mutation status was negative in all cases. CONCLUSION: Symptoms fitting the criteria for possible behavioral variant frontotemporal dementia may be present in end-stage of bipolar disorder. An alternative neurodegenerative nature seems unlikely based on repeated normal neuroimaging and the absence of clinical progression. Functional involvement of the frontal-subcortical networks might play a role. Dove Medical Press 2016-09-07 /pmc/articles/PMC5019473/ /pubmed/27660450 http://dx.doi.org/10.2147/NDT.S99229 Text en © 2016 Dols et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Case Series
Dols, Annemiek
Krudop, Welmoed
Möller, Christiane
Shulman, Kenneth
Sajatovic, Martha
Pijnenburg, Yolande AL
Late life bipolar disorder evolving into frontotemporal dementia mimic
title Late life bipolar disorder evolving into frontotemporal dementia mimic
title_full Late life bipolar disorder evolving into frontotemporal dementia mimic
title_fullStr Late life bipolar disorder evolving into frontotemporal dementia mimic
title_full_unstemmed Late life bipolar disorder evolving into frontotemporal dementia mimic
title_short Late life bipolar disorder evolving into frontotemporal dementia mimic
title_sort late life bipolar disorder evolving into frontotemporal dementia mimic
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019473/
https://www.ncbi.nlm.nih.gov/pubmed/27660450
http://dx.doi.org/10.2147/NDT.S99229
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