Late-life cynical hostility is associated with white matter alterations and the risk of Alzheimer's disease.

Alzheimer Disease Cerebral white matter Personality cohort corpus callosum risk factor

Journal

Psychological medicine
ISSN: 1469-8978
Titre abrégé: Psychol Med
Pays: England
ID NLM: 1254142

Informations de publication

Date de publication:
14 Apr 2021
Historique:
entrez: 14 4 2021
pubmed: 15 4 2021
medline: 15 4 2021
Statut: aheadofprint

Résumé

Cynical hostility (CH), a specific dimension of hostility that consists of a mistrust of others, has been suggested as a high-risk trait for dementia. However, the influence of CH on the incidence of Alzheimer's disease (AD) remains poorly understood. This study investigated whether late-life CH is associated with AD risk and structural neuroimaging markers of AD. In community-dwelling older adults from the French ESPRIT cohort (n = 1388), incident dementia rate according to CH level was monitored during an 8-year follow-up and analyzed using Cox proportional hazards regression models. Brain magnetic resonance imaging volumes were measured at baseline (n = 508). Using automated segmentation procedures (Freesurfer 6.0), the authors assessed brain grey and white volumes on all magnetic resonance imaging scans. They also measured white matter hyperintensities volumes using semi-automated procedures. Mean volumes according to the level of CH were compared using ANOVA. Eighty-four participants developed dementia (32 with AD). After controlling for potential confounders, high CH was predictive of AD (HR 2.74; 95% CI 1.10-6.85; p = 0.030) and all dementia types are taken together (HR 2.30; 95% CI 1.10-4.80; p = 0.027). High CH was associated with white matter alterations, particularly smaller anterior corpus callosum volume (p < 0.01) after False Discovery Rate correction, but not with grey matter volumes. High CH in late life is associated with cerebral white matter alterations, designated as early markers of dementia, and higher AD risk. Identifying lifestyle and biological determinants related to CH could provide clues on AD physiopathology and avenues for prevention strategies.

Sections du résumé

BACKGROUND BACKGROUND
Cynical hostility (CH), a specific dimension of hostility that consists of a mistrust of others, has been suggested as a high-risk trait for dementia. However, the influence of CH on the incidence of Alzheimer's disease (AD) remains poorly understood. This study investigated whether late-life CH is associated with AD risk and structural neuroimaging markers of AD.
METHODS METHODS
In community-dwelling older adults from the French ESPRIT cohort (n = 1388), incident dementia rate according to CH level was monitored during an 8-year follow-up and analyzed using Cox proportional hazards regression models. Brain magnetic resonance imaging volumes were measured at baseline (n = 508). Using automated segmentation procedures (Freesurfer 6.0), the authors assessed brain grey and white volumes on all magnetic resonance imaging scans. They also measured white matter hyperintensities volumes using semi-automated procedures. Mean volumes according to the level of CH were compared using ANOVA.
RESULTS RESULTS
Eighty-four participants developed dementia (32 with AD). After controlling for potential confounders, high CH was predictive of AD (HR 2.74; 95% CI 1.10-6.85; p = 0.030) and all dementia types are taken together (HR 2.30; 95% CI 1.10-4.80; p = 0.027). High CH was associated with white matter alterations, particularly smaller anterior corpus callosum volume (p < 0.01) after False Discovery Rate correction, but not with grey matter volumes.
CONCLUSIONS CONCLUSIONS
High CH in late life is associated with cerebral white matter alterations, designated as early markers of dementia, and higher AD risk. Identifying lifestyle and biological determinants related to CH could provide clues on AD physiopathology and avenues for prevention strategies.

Identifiants

pubmed: 33849668
doi: 10.1017/S0033291721000416
pii: S0033291721000416
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-10

Auteurs

Fabienne Cyprien (F)

IGF, Univ Montpellier, CNRS, INSERM, Montpellier, France.
CHU Montpellier, Montpellier, France.

Claudine Berr (C)

INM, Univ Montpellier, INSERM, Montpellier, France.

Jerome J Maller (JJ)

Monash Alfred Psychiatry Research Centre, The Alfred & Monash University School of Psychology and Psychiatry, Melbourne, Australia.

Chantal Meslin (C)

Centre for Mental Health Research, Australian National University, Canberra, Australia.

Mélissa Gentreau (M)

IGF, Univ Montpellier, CNRS, INSERM, Montpellier, France.

Thibault Mura (T)

INM, Univ Montpellier, INSERM, Montpellier, France.
CHU Nîmes, Nîmes, France.

Audrey Gabelle (A)

CHU Montpellier, Montpellier, France.
INM, Univ Montpellier, INSERM, Montpellier, France.

Philippe Courtet (P)

IGF, Univ Montpellier, CNRS, INSERM, Montpellier, France.
CHU Montpellier, Montpellier, France.

Karen Ritchie (K)

INM, Univ Montpellier, INSERM, Montpellier, France.
Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.

Marie-Laure Ancelin (ML)

INM, Univ Montpellier, INSERM, Montpellier, France.

Sylvaine Artero (S)

IGF, Univ Montpellier, CNRS, INSERM, Montpellier, France.

Classifications MeSH