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Contribution of neuroimaging in late-life depression

ABSTRACT: Late-life depression (LLD) is currently a hot topic for neuroimaging studies, while an increasing number of imaging modalities are now available for the characterization of brain structure and function. Changes in brain volumes, including hippocampal volume, have been observed in LLD, alth...

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Autor principal: Desmidt, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417497/
http://dx.doi.org/10.1192/j.eurpsy.2023.56
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author Desmidt, T.
author_facet Desmidt, T.
author_sort Desmidt, T.
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description ABSTRACT: Late-life depression (LLD) is currently a hot topic for neuroimaging studies, while an increasing number of imaging modalities are now available for the characterization of brain structure and function. Changes in brain volumes, including hippocampal volume, have been observed in LLD, although results are inconsistent. Vascular lesions are more consistently associated with LLD and may constitute factors of poor prognosis. More recent MRI modalities, including fMRI and DTI, also show interesting results, notably to assess treatment response in LLD. Molecular Imaging also has the potential to improve our understanding of the pathophysiology of LLD, using imaging such as PET-FDG and Amyloid PET. Finally, there are emerging studies with novel neuroimaging modalities such as Ultrasound to measure subtle mechanical properties in the brain of patients with LLD. Finally, we contend that neuroimaging has the potential to provide markers for the identification of subcategories of LLD (vascular depression, amyloid depression, etc.) as well as prognostic values and markers for treatment response. DISCLOSURE OF INTEREST: None Declared
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spelling pubmed-104174972023-08-12 Contribution of neuroimaging in late-life depression Desmidt, T. Eur Psychiatry Abstract ABSTRACT: Late-life depression (LLD) is currently a hot topic for neuroimaging studies, while an increasing number of imaging modalities are now available for the characterization of brain structure and function. Changes in brain volumes, including hippocampal volume, have been observed in LLD, although results are inconsistent. Vascular lesions are more consistently associated with LLD and may constitute factors of poor prognosis. More recent MRI modalities, including fMRI and DTI, also show interesting results, notably to assess treatment response in LLD. Molecular Imaging also has the potential to improve our understanding of the pathophysiology of LLD, using imaging such as PET-FDG and Amyloid PET. Finally, there are emerging studies with novel neuroimaging modalities such as Ultrasound to measure subtle mechanical properties in the brain of patients with LLD. Finally, we contend that neuroimaging has the potential to provide markers for the identification of subcategories of LLD (vascular depression, amyloid depression, etc.) as well as prognostic values and markers for treatment response. DISCLOSURE OF INTEREST: None Declared Cambridge University Press 2023-07-19 /pmc/articles/PMC10417497/ http://dx.doi.org/10.1192/j.eurpsy.2023.56 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Desmidt, T.
Contribution of neuroimaging in late-life depression
title Contribution of neuroimaging in late-life depression
title_full Contribution of neuroimaging in late-life depression
title_fullStr Contribution of neuroimaging in late-life depression
title_full_unstemmed Contribution of neuroimaging in late-life depression
title_short Contribution of neuroimaging in late-life depression
title_sort contribution of neuroimaging in late-life depression
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417497/
http://dx.doi.org/10.1192/j.eurpsy.2023.56
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