Sex-specificities in anxiety and depressive symptoms across the lifespan and their links with multimodal neuroimaging.


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
01 01 2022
Historique:
received: 14 06 2021
revised: 03 10 2021
accepted: 06 10 2021
pubmed: 13 10 2021
medline: 27 1 2022
entrez: 12 10 2021
Statut: ppublish

Résumé

Anxiety and depressive symptoms are associated with impaired well-being, higher risk of developing psychoaffective disorders and are risk factors for Alzheimer's disease (AD). To further understand their relevance and the mechanisms underlying their link with AD, our aims were to assess how anxiety and depressive symptoms changed with age and related to AD neuroimaging biomarkers across the adult lifespan, while also exploring sex specificities. 210 cognitively normal participants aged 19-86 years (101 men, 109 women) completed assessments of anxiety and depressive symptoms with the STAI-A and MADRS respectively, and neuroimaging measurements including structural MRI, FDG-PET and amyloid-PET. 167 of those were followed-up over 1.5-3 years. Multiple regressions were performed to assess the links between anxiety or depressive symptoms versus age, global cognition or each imaging modality, both cross-sectionally and longitudinally; and general linear models we used to test the interactive effect of sex on these associations. Depressive symptoms decreased with age, while anxiety symptoms increased only among women. Higher anxiety symptoms were associated with lower grey matter (GM) volume and glucose metabolism, with an interaction of sex, this relationship being significant only in women. Longitudinally, only low baseline GM volume predicted an increase in anxiety symptoms with time. Only 43% of participants reported depressive symptoms. Despite additional analyses, the low variability in the measure might have prevented us from detecting subtle changes. This study emphasizes the need to consider anxiety symptoms in assessments for dementia risk, particularly in women.

Sections du résumé

BACKGROUND
Anxiety and depressive symptoms are associated with impaired well-being, higher risk of developing psychoaffective disorders and are risk factors for Alzheimer's disease (AD). To further understand their relevance and the mechanisms underlying their link with AD, our aims were to assess how anxiety and depressive symptoms changed with age and related to AD neuroimaging biomarkers across the adult lifespan, while also exploring sex specificities.
METHODS
210 cognitively normal participants aged 19-86 years (101 men, 109 women) completed assessments of anxiety and depressive symptoms with the STAI-A and MADRS respectively, and neuroimaging measurements including structural MRI, FDG-PET and amyloid-PET. 167 of those were followed-up over 1.5-3 years. Multiple regressions were performed to assess the links between anxiety or depressive symptoms versus age, global cognition or each imaging modality, both cross-sectionally and longitudinally; and general linear models we used to test the interactive effect of sex on these associations.
RESULTS
Depressive symptoms decreased with age, while anxiety symptoms increased only among women. Higher anxiety symptoms were associated with lower grey matter (GM) volume and glucose metabolism, with an interaction of sex, this relationship being significant only in women. Longitudinally, only low baseline GM volume predicted an increase in anxiety symptoms with time.
LIMITATIONS
Only 43% of participants reported depressive symptoms. Despite additional analyses, the low variability in the measure might have prevented us from detecting subtle changes.
CONCLUSIONS
This study emphasizes the need to consider anxiety symptoms in assessments for dementia risk, particularly in women.

Identifiants

pubmed: 34637806
pii: S0165-0327(21)01072-7
doi: 10.1016/j.jad.2021.10.004
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

593-602

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Inès Moulinet (I)

Normandie Univ, UNICAEN, INSERM, U1237, PhIND Physiopathology and Imaging of Neurological Disorders, Institute Blood and Brain @ Caen-Normandie (BB@C), GIP Cyceron, 4 Bvd Henri Becquerel, Caen 14000, France.

Brigitte Landeau (B)

Normandie Univ, UNICAEN, INSERM, U1237, PhIND Physiopathology and Imaging of Neurological Disorders, Institute Blood and Brain @ Caen-Normandie (BB@C), GIP Cyceron, 4 Bvd Henri Becquerel, Caen 14000, France.

Edelweiss Touron (E)

Normandie Univ, UNICAEN, INSERM, U1237, PhIND Physiopathology and Imaging of Neurological Disorders, Institute Blood and Brain @ Caen-Normandie (BB@C), GIP Cyceron, 4 Bvd Henri Becquerel, Caen 14000, France.

Vincent De La Sayette (V)

Normandie Univ, UNICAEN, EPHE, INSERM, U1077, PSL Recherche Universités, CHU de Caen, Neuropsychologie et Imagerie de la Mémoire Humaine, GIP Cyceron, Caen 14000, France; Service de Neurologie, CHU de Caen, Caen, France.

Béatrice Desgranges (B)

Normandie Univ, UNICAEN, EPHE, INSERM, U1077, PSL Recherche Universités, CHU de Caen, Neuropsychologie et Imagerie de la Mémoire Humaine, GIP Cyceron, Caen 14000, France.

Denis Vivien (D)

Normandie Univ, UNICAEN, INSERM, U1237, PhIND Physiopathology and Imaging of Neurological Disorders, Institute Blood and Brain @ Caen-Normandie (BB@C), GIP Cyceron, 4 Bvd Henri Becquerel, Caen 14000, France; Department of Clinical Research, Caen Normandy Hospital (CHU) de Caen, Caen 14000, France.

Natalie Marchant (N)

Division of Psychiatry, University College London, London, United Kingdom.

Géraldine Poisnel (G)

Normandie Univ, UNICAEN, INSERM, U1237, PhIND Physiopathology and Imaging of Neurological Disorders, Institute Blood and Brain @ Caen-Normandie (BB@C), GIP Cyceron, 4 Bvd Henri Becquerel, Caen 14000, France.

Gaël Chételat (G)

Normandie Univ, UNICAEN, INSERM, U1237, PhIND Physiopathology and Imaging of Neurological Disorders, Institute Blood and Brain @ Caen-Normandie (BB@C), GIP Cyceron, 4 Bvd Henri Becquerel, Caen 14000, France. Electronic address: chetelat@cyceron.fr.

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