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The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum

INTRODUCTION: Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two phenotypes of the same neurodegenerative disease, the FTD-ALS spectrum. What determines the development of one rather than the other phenotype is still unknown. Based on the clinical observation that patients...

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Autores principales: Vinceti, Giulia, Carbone, Chiara, Gallingani, Chiara, Fiondella, Luigi, Salemme, Simone, Zucchi, Elisabetta, Martinelli, Ilaria, Gianferrari, Giulia, Tondelli, Manuela, Mandrioli, Jessica, Chiari, Annalisa, Zamboni, Giovanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582748/
https://www.ncbi.nlm.nih.gov/pubmed/37859765
http://dx.doi.org/10.3389/fnins.2023.1248622
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author Vinceti, Giulia
Carbone, Chiara
Gallingani, Chiara
Fiondella, Luigi
Salemme, Simone
Zucchi, Elisabetta
Martinelli, Ilaria
Gianferrari, Giulia
Tondelli, Manuela
Mandrioli, Jessica
Chiari, Annalisa
Zamboni, Giovanna
author_facet Vinceti, Giulia
Carbone, Chiara
Gallingani, Chiara
Fiondella, Luigi
Salemme, Simone
Zucchi, Elisabetta
Martinelli, Ilaria
Gianferrari, Giulia
Tondelli, Manuela
Mandrioli, Jessica
Chiari, Annalisa
Zamboni, Giovanna
author_sort Vinceti, Giulia
collection PubMed
description INTRODUCTION: Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two phenotypes of the same neurodegenerative disease, the FTD-ALS spectrum. What determines the development of one rather than the other phenotype is still unknown. Based on the clinical observation that patients’ personality seems to differ between the two phenotypes, i.e., ALS patients tend to display kind, prosocial behaviors whereas FTD patients tend to present anti-social behaviors, and that these traits are often reported as pre-existing the disease onset by caregivers, we set up to study experimentally patients’ personality in their premorbid life. METHODS: We first tested for differences between groups, then tested the association between premorbid personality and current functional organization of the brain. Premorbid personality of a cohort of forty patients, 27 FTD and 13 ALS, was explored through the NEO Personality Inventory 3 (NEO-PI-3), which analyses the five main personality factors, completed by the caregiver with reference to patient’s personality 20 years before symptoms onset (premorbid). A subgroup of patients underwent a brain MRI including structural and resting-state functional MRI (rsfMRI). RESULTS: A significant difference between FTD and ALS in premorbid personality emerged in the Openness (133.92 FTD vs. 149.84 ALS, p = 0.01) and Extraversion (136.55 FTD vs. 150.53 ALS, p = 0.04) factors. This suggests that ALS patients had been, in their premorbid life, more open to new experiences, more sociable and optimistic than FTD patients. They also showed greater functional connectivity than both FTD and a control group in the Salience resting state network, over and above differences in gray matter atrophy. Finally, there was a positive correlation between premorbid Openness and functional connectivity in the Salience network across all patients, suggesting a possible association between premorbid personality and current functional organization of the brain, irrespective of the degree of atrophy. DISCUSSION: Our proof-of-concept results suggest that premorbid personality may eventually predispose to the development of one, rather than the other, phenotype in the FTD-ALS spectrum.
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spelling pubmed-105827482023-10-19 The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum Vinceti, Giulia Carbone, Chiara Gallingani, Chiara Fiondella, Luigi Salemme, Simone Zucchi, Elisabetta Martinelli, Ilaria Gianferrari, Giulia Tondelli, Manuela Mandrioli, Jessica Chiari, Annalisa Zamboni, Giovanna Front Neurosci Neuroscience INTRODUCTION: Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two phenotypes of the same neurodegenerative disease, the FTD-ALS spectrum. What determines the development of one rather than the other phenotype is still unknown. Based on the clinical observation that patients’ personality seems to differ between the two phenotypes, i.e., ALS patients tend to display kind, prosocial behaviors whereas FTD patients tend to present anti-social behaviors, and that these traits are often reported as pre-existing the disease onset by caregivers, we set up to study experimentally patients’ personality in their premorbid life. METHODS: We first tested for differences between groups, then tested the association between premorbid personality and current functional organization of the brain. Premorbid personality of a cohort of forty patients, 27 FTD and 13 ALS, was explored through the NEO Personality Inventory 3 (NEO-PI-3), which analyses the five main personality factors, completed by the caregiver with reference to patient’s personality 20 years before symptoms onset (premorbid). A subgroup of patients underwent a brain MRI including structural and resting-state functional MRI (rsfMRI). RESULTS: A significant difference between FTD and ALS in premorbid personality emerged in the Openness (133.92 FTD vs. 149.84 ALS, p = 0.01) and Extraversion (136.55 FTD vs. 150.53 ALS, p = 0.04) factors. This suggests that ALS patients had been, in their premorbid life, more open to new experiences, more sociable and optimistic than FTD patients. They also showed greater functional connectivity than both FTD and a control group in the Salience resting state network, over and above differences in gray matter atrophy. Finally, there was a positive correlation between premorbid Openness and functional connectivity in the Salience network across all patients, suggesting a possible association between premorbid personality and current functional organization of the brain, irrespective of the degree of atrophy. DISCUSSION: Our proof-of-concept results suggest that premorbid personality may eventually predispose to the development of one, rather than the other, phenotype in the FTD-ALS spectrum. Frontiers Media S.A. 2023-10-04 /pmc/articles/PMC10582748/ /pubmed/37859765 http://dx.doi.org/10.3389/fnins.2023.1248622 Text en Copyright © 2023 Vinceti, Carbone, Gallingani, Fiondella, Salemme, Zucchi, Martinelli, Gianferrari, Tondelli, Mandrioli, Chiari and Zamboni. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Vinceti, Giulia
Carbone, Chiara
Gallingani, Chiara
Fiondella, Luigi
Salemme, Simone
Zucchi, Elisabetta
Martinelli, Ilaria
Gianferrari, Giulia
Tondelli, Manuela
Mandrioli, Jessica
Chiari, Annalisa
Zamboni, Giovanna
The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum
title The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum
title_full The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum
title_fullStr The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum
title_full_unstemmed The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum
title_short The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum
title_sort association between lifelong personality and clinical phenotype in the ftd-als spectrum
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582748/
https://www.ncbi.nlm.nih.gov/pubmed/37859765
http://dx.doi.org/10.3389/fnins.2023.1248622
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