Cargando…

Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia

IMPORTANCE: The neurological substrates of visual artistic creativity (VAC) are unknown. VAC is demonstrated here to occur early in frontotemporal dementia (FTD), and multimodal neuroimaging is used to generate a novel mechanistic hypothesis involving dorsomedial occipital cortex enhancement. These...

Descripción completa

Detalles Bibliográficos
Autores principales: Friedberg, Adit, Pasquini, Lorenzo, Diggs, Ryan, Glaubitz, Erika A., Lopez, Lucia, Illán-Gala, Ignacio, Iaccarino, Leonardo, La Joie, Renaud, Mundada, Nidhi, Knudtson, Marguerite, Neylan, Kyra, Brown, Jesse, Allen, Isabel Elaine, Rankin, Katherine P., Bonham, Luke W., Yokoyama, Jennifer S., Ramos, Eliana M., Geschwind, Daniel H., Spina, Salvatore, Grinberg, Lea T., Miller, Zachary A., Kramer, Joel H., Rosen, Howard, Gorno-Tempini, Maria Luisa, Rabinovici, Gil, Seeley, William W., Miller, Bruce L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972248/
https://www.ncbi.nlm.nih.gov/pubmed/36848111
http://dx.doi.org/10.1001/jamaneurol.2023.0001
_version_ 1784898281011150848
author Friedberg, Adit
Pasquini, Lorenzo
Diggs, Ryan
Glaubitz, Erika A.
Lopez, Lucia
Illán-Gala, Ignacio
Iaccarino, Leonardo
La Joie, Renaud
Mundada, Nidhi
Knudtson, Marguerite
Neylan, Kyra
Brown, Jesse
Allen, Isabel Elaine
Rankin, Katherine P.
Bonham, Luke W.
Yokoyama, Jennifer S.
Ramos, Eliana M.
Geschwind, Daniel H.
Spina, Salvatore
Grinberg, Lea T.
Miller, Zachary A.
Kramer, Joel H.
Rosen, Howard
Gorno-Tempini, Maria Luisa
Rabinovici, Gil
Seeley, William W.
Miller, Bruce L.
author_facet Friedberg, Adit
Pasquini, Lorenzo
Diggs, Ryan
Glaubitz, Erika A.
Lopez, Lucia
Illán-Gala, Ignacio
Iaccarino, Leonardo
La Joie, Renaud
Mundada, Nidhi
Knudtson, Marguerite
Neylan, Kyra
Brown, Jesse
Allen, Isabel Elaine
Rankin, Katherine P.
Bonham, Luke W.
Yokoyama, Jennifer S.
Ramos, Eliana M.
Geschwind, Daniel H.
Spina, Salvatore
Grinberg, Lea T.
Miller, Zachary A.
Kramer, Joel H.
Rosen, Howard
Gorno-Tempini, Maria Luisa
Rabinovici, Gil
Seeley, William W.
Miller, Bruce L.
author_sort Friedberg, Adit
collection PubMed
description IMPORTANCE: The neurological substrates of visual artistic creativity (VAC) are unknown. VAC is demonstrated here to occur early in frontotemporal dementia (FTD), and multimodal neuroimaging is used to generate a novel mechanistic hypothesis involving dorsomedial occipital cortex enhancement. These findings may illuminate a novel mechanism underlying human visual creativity. OBJECTIVE: To determine the anatomical and physiological underpinnings of VAC in FTD. DESIGN, SETTING, AND PARTICIPANTS: This case-control study analyzed records of 689 patients who met research criteria for an FTD spectrum disorder between 2002 and 2019. Individuals with FTD and emergence of visual artistic creativity (VAC-FTD) were matched to 2 control groups based on demographic and clinical parameters: (1) not visually artistic FTD (NVA-FTD) and (2) healthy controls (HC). Analysis took place between September 2019 to December 2021. MAIN OUTCOMES AND MEASURES: Clinical, neuropsychological, genetic, and neuroimaging data were analyzed to characterize VAC-FTD and compare VAC-FTD with control groups. RESULTS: Of 689 patients with FTD, 17 (2.5%) met VAC-FTD inclusion criteria (mean [SD] age, 65 [9.7] years; 10 [58.8%] female). NVA-FTD (n = 51; mean [SD] age, 64.8 [7] years; 25 [49.0%] female) and HC (n = 51; mean [SD] age, 64.5 [7.2] years; 25 [49%] female) groups were well matched to VAC-FTD demographically. Emergence of VAC occurred around the time of onset of symptoms and was disproportionately seen in patients with temporal lobe predominant degeneration (8 of 17 [47.1%]). Atrophy network mapping identified a dorsomedial occipital region whose activity inversely correlated, in healthy brains, with activity in regions found within the patient-specific atrophy patterns in VAC-FTD (17 of 17) and NVA-FTD (45 of 51 [88.2%]). Structural covariance analysis revealed that the volume of this dorsal occipital region was strongly correlated in VAC-FTD, but not in NVA-FTD or HC, with a volume in the primary motor cortex corresponding to the right-hand representation. CONCLUSIONS AND RELEVANCE: This study generated a novel hypothesis about the mechanisms underlying the emergence of VAC in FTD. These findings suggest that early lesion-induced activation of dorsal visual association areas may predispose some patients to the emergence of VAC under certain environmental or genetic conditions. This work sets the stage for further exploration of enhanced capacities arising early in the course of neurodegeneration.
format Online
Article
Text
id pubmed-9972248
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Medical Association
record_format MEDLINE/PubMed
spelling pubmed-99722482023-03-01 Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia Friedberg, Adit Pasquini, Lorenzo Diggs, Ryan Glaubitz, Erika A. Lopez, Lucia Illán-Gala, Ignacio Iaccarino, Leonardo La Joie, Renaud Mundada, Nidhi Knudtson, Marguerite Neylan, Kyra Brown, Jesse Allen, Isabel Elaine Rankin, Katherine P. Bonham, Luke W. Yokoyama, Jennifer S. Ramos, Eliana M. Geschwind, Daniel H. Spina, Salvatore Grinberg, Lea T. Miller, Zachary A. Kramer, Joel H. Rosen, Howard Gorno-Tempini, Maria Luisa Rabinovici, Gil Seeley, William W. Miller, Bruce L. JAMA Neurol Original Investigation IMPORTANCE: The neurological substrates of visual artistic creativity (VAC) are unknown. VAC is demonstrated here to occur early in frontotemporal dementia (FTD), and multimodal neuroimaging is used to generate a novel mechanistic hypothesis involving dorsomedial occipital cortex enhancement. These findings may illuminate a novel mechanism underlying human visual creativity. OBJECTIVE: To determine the anatomical and physiological underpinnings of VAC in FTD. DESIGN, SETTING, AND PARTICIPANTS: This case-control study analyzed records of 689 patients who met research criteria for an FTD spectrum disorder between 2002 and 2019. Individuals with FTD and emergence of visual artistic creativity (VAC-FTD) were matched to 2 control groups based on demographic and clinical parameters: (1) not visually artistic FTD (NVA-FTD) and (2) healthy controls (HC). Analysis took place between September 2019 to December 2021. MAIN OUTCOMES AND MEASURES: Clinical, neuropsychological, genetic, and neuroimaging data were analyzed to characterize VAC-FTD and compare VAC-FTD with control groups. RESULTS: Of 689 patients with FTD, 17 (2.5%) met VAC-FTD inclusion criteria (mean [SD] age, 65 [9.7] years; 10 [58.8%] female). NVA-FTD (n = 51; mean [SD] age, 64.8 [7] years; 25 [49.0%] female) and HC (n = 51; mean [SD] age, 64.5 [7.2] years; 25 [49%] female) groups were well matched to VAC-FTD demographically. Emergence of VAC occurred around the time of onset of symptoms and was disproportionately seen in patients with temporal lobe predominant degeneration (8 of 17 [47.1%]). Atrophy network mapping identified a dorsomedial occipital region whose activity inversely correlated, in healthy brains, with activity in regions found within the patient-specific atrophy patterns in VAC-FTD (17 of 17) and NVA-FTD (45 of 51 [88.2%]). Structural covariance analysis revealed that the volume of this dorsal occipital region was strongly correlated in VAC-FTD, but not in NVA-FTD or HC, with a volume in the primary motor cortex corresponding to the right-hand representation. CONCLUSIONS AND RELEVANCE: This study generated a novel hypothesis about the mechanisms underlying the emergence of VAC in FTD. These findings suggest that early lesion-induced activation of dorsal visual association areas may predispose some patients to the emergence of VAC under certain environmental or genetic conditions. This work sets the stage for further exploration of enhanced capacities arising early in the course of neurodegeneration. American Medical Association 2023-02-27 2023-04 /pmc/articles/PMC9972248/ /pubmed/36848111 http://dx.doi.org/10.1001/jamaneurol.2023.0001 Text en Copyright 2023 Friedberg A et al. JAMA Neurology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Friedberg, Adit
Pasquini, Lorenzo
Diggs, Ryan
Glaubitz, Erika A.
Lopez, Lucia
Illán-Gala, Ignacio
Iaccarino, Leonardo
La Joie, Renaud
Mundada, Nidhi
Knudtson, Marguerite
Neylan, Kyra
Brown, Jesse
Allen, Isabel Elaine
Rankin, Katherine P.
Bonham, Luke W.
Yokoyama, Jennifer S.
Ramos, Eliana M.
Geschwind, Daniel H.
Spina, Salvatore
Grinberg, Lea T.
Miller, Zachary A.
Kramer, Joel H.
Rosen, Howard
Gorno-Tempini, Maria Luisa
Rabinovici, Gil
Seeley, William W.
Miller, Bruce L.
Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia
title Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia
title_full Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia
title_fullStr Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia
title_full_unstemmed Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia
title_short Prevalence, Timing, and Network Localization of Emergent Visual Creativity in Frontotemporal Dementia
title_sort prevalence, timing, and network localization of emergent visual creativity in frontotemporal dementia
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972248/
https://www.ncbi.nlm.nih.gov/pubmed/36848111
http://dx.doi.org/10.1001/jamaneurol.2023.0001
work_keys_str_mv AT friedbergadit prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT pasquinilorenzo prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT diggsryan prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT glaubitzerikaa prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT lopezlucia prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT illangalaignacio prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT iaccarinoleonardo prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT lajoierenaud prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT mundadanidhi prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT knudtsonmarguerite prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT neylankyra prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT brownjesse prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT allenisabelelaine prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT rankinkatherinep prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT bonhamlukew prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT yokoyamajennifers prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT ramoselianam prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT geschwinddanielh prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT spinasalvatore prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT grinbergleat prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT millerzacharya prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT kramerjoelh prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT rosenhoward prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT gornotempinimarialuisa prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT rabinovicigil prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT seeleywilliamw prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia
AT millerbrucel prevalencetimingandnetworklocalizationofemergentvisualcreativityinfrontotemporaldementia