The key role of depression and supramarginal gyrus in frailty: a cross-sectional study.

MRI aging brain cognitive impairment depression frailty supramarginal gyrus

Journal

Frontiers in aging neuroscience
ISSN: 1663-4365
Titre abrégé: Front Aging Neurosci
Pays: Switzerland
ID NLM: 101525824

Informations de publication

Date de publication:
2023
Historique:
received: 15 09 2023
accepted: 26 10 2023
medline: 29 11 2023
pubmed: 29 11 2023
entrez: 29 11 2023
Statut: epublish

Résumé

The age-related decrease in reserve and resistance to stressors is recognized as frailty, one of the most significant challenges identified in recent years. Despite a well-acknowledged association of frailty with cognitive impairment, depression, and gray matter morphology, no clear data are available regarding the nature of this relationship. This cross-sectional study aims to disentangle the role of the behavioral, neuropsychological, and neural components as predictors or moderators of frailty. Ninety-six older adults (mean age = 75.49 ± 6.62) were consecutively enrolled and underwent a clinical and MRI (3 T) evaluation to assess frailty, physical activity, global cognitive level, depression, wellbeing, autonomy in daily living, cortical thickness, and subcortical volumes. Results showed a full mediation of depression on the link between cortical thickness and frailty, while the cognitive level showed no significant mediating role. In particular, left supramarginal thickness had a predicting role on depression, that in turn impacted frailty occurrence. Finally, handgrip weakness was an early key indicator of frailty in this study's cohort. These data substantiate the role of depression in mediating the link between neural integrity of the supramarginal gyrus and frailty. In the complexity of frailty, handgrip weakness seems to be an early key indicator. These results are relevant for the design of rehabilitation interventions aimed at reversing the frail condition.

Sections du résumé

Background UNASSIGNED
The age-related decrease in reserve and resistance to stressors is recognized as frailty, one of the most significant challenges identified in recent years. Despite a well-acknowledged association of frailty with cognitive impairment, depression, and gray matter morphology, no clear data are available regarding the nature of this relationship. This cross-sectional study aims to disentangle the role of the behavioral, neuropsychological, and neural components as predictors or moderators of frailty.
Methods UNASSIGNED
Ninety-six older adults (mean age = 75.49 ± 6.62) were consecutively enrolled and underwent a clinical and MRI (3 T) evaluation to assess frailty, physical activity, global cognitive level, depression, wellbeing, autonomy in daily living, cortical thickness, and subcortical volumes.
Results UNASSIGNED
Results showed a full mediation of depression on the link between cortical thickness and frailty, while the cognitive level showed no significant mediating role. In particular, left supramarginal thickness had a predicting role on depression, that in turn impacted frailty occurrence. Finally, handgrip weakness was an early key indicator of frailty in this study's cohort.
Conclusion UNASSIGNED
These data substantiate the role of depression in mediating the link between neural integrity of the supramarginal gyrus and frailty. In the complexity of frailty, handgrip weakness seems to be an early key indicator. These results are relevant for the design of rehabilitation interventions aimed at reversing the frail condition.

Identifiants

pubmed: 38020757
doi: 10.3389/fnagi.2023.1292417
pmc: PMC10665836
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1292417

Informations de copyright

Copyright © 2023 Isernia, Blasi, Baglio, Cabinio, Cecconi, Rossetto, Cazzoli, Blasi, Bruckmann, Giunco, Sorbi, Clerici and Baglio.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Sara Isernia (S)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Valeria Blasi (V)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Gisella Baglio (G)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Monia Cabinio (M)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Pietro Cecconi (P)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Federica Rossetto (F)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Marta Cazzoli (M)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Francesco Blasi (F)

Fondazione Istituto FIRC di Oncologia Molecolare, Milan, Italy.

Chiara Bruckmann (C)

Fondazione Istituto FIRC di Oncologia Molecolare, Milan, Italy.

Fabrizio Giunco (F)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Sandro Sorbi (S)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Mario Clerici (M)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.

Francesca Baglio (F)

IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.

Classifications MeSH