» Articles » PMID: 35599483

Gender/Sex Differences in the Association of Mild Behavioral Impairment with Cognitive Aging

Overview
Publisher Sage Publications
Specialties Geriatrics
Neurology
Date 2022 May 23
PMID 35599483
Authors
Affiliations
Soon will be listed here.
Abstract

Background: While the gender/sex differences in neuropsychiatric symptoms in dementia population are well described, gender/sex differences in mild behavioral impairment (MBI) in dementia-free populations and the relationship to cognitive performance and to subsequent cognitive decline have not been studied.

Objective: We aimed to explore gender/sex differences in the association of MBI with the level of cognitive performance and its rate of decline in a dementia-free cohort.

Methods: We studied 8,181 older adults enrolled in the online PROTECT UK Study. MBI was assessed using the MBI Checklist and cognition was measured by digit span, paired associate learning, spatial working memory, and verbal reasoning. Statistical analysis was conducted using linear regression models and linear mixed-effects models.

Results: Out of 8,181 individuals (median age 63 years, 73% females), 11% of females and 14% of males had MBI syndrome. Females exhibited less often symptoms of decreased motivation (45% versus 36% in males), impulse dyscontrol (40% versus 44% in males; p = 0.001) and social inappropriateness (12% versus 15%; p < 0.001), while they showed more often symptoms of emotional dysregulation (45% versus 36%; p < 0.001). The associations of MBI domains with some measures of cognitive performance and decline were stronger in males than females, with the exception of the association of emotional dysregulation with the rate of cognitive decline in verbal reasoning, which was present exclusively in females.

Conclusion: MBI may influence cognition to a greater extent in males than in females. We propose that predictors and biomarkers of dementia should consider gender/sex as an effect modifier.

Citing Articles

Menopausal symptom burden as a predictor of mid- to late-life cognitive function and mild behavioral impairment symptoms: A CAN-PROTECT study.

Crockford J, Guan D, Einstein G, Ballard C, Creese B, Corbett A PLoS One. 2025; 20(3):e0301165.

PMID: 40043017 PMC: 11882070. DOI: 10.1371/journal.pone.0301165.


Synaptic vulnerability to amyloid-β and tau pathologies differentially disrupts emotional and memory neural circuits.

Capilla-Lopez M, Deprada A, Andrade-Talavera Y, Martinez-Gallego I, Coatl-Cuaya H, Sotillo P Mol Psychiatry. 2025; .

PMID: 39885298 DOI: 10.1038/s41380-025-02901-9.


Possible influence of sex on the relationship between dual-task gait costs and cognitive decline in older adults.

Christova M, Fresnoza S, Palli C, Staubmann W, Guggenberger B PLoS One. 2025; 20(1):e0317365.

PMID: 39883741 PMC: 11781657. DOI: 10.1371/journal.pone.0317365.


Inflammaging and Brain Aging.

Jurcau M, Jurcau A, Cristian A, Hogea V, Diaconu R, Nunkoo V Int J Mol Sci. 2024; 25(19).

PMID: 39408862 PMC: 11476611. DOI: 10.3390/ijms251910535.


Linking cognitive and behavioral reserve: Evidence from the CAN-PROTECT study.

Guan D, Mortby M, Pike G, Ballard C, Creese B, Corbett A Alzheimers Dement (N Y). 2024; 10(4):e12497.

PMID: 39372373 PMC: 11450604. DOI: 10.1002/trc2.12497.