Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Mehta, Kanikaa; b | Mohebbi, Mohammadrezaa; c | Pasco, Julie A.a; d; e; f | Williams, Lana J.a; f | Walder, Kena | Ng, Boon Lungg | Gupta, Veer Balaa; *
Affiliations: [a] Deakin University, IMPACT – The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Geelong, VIC, Australia | [b] Baker Heart and Diabetes Institute, Melbourne, VIC, Australia | [c] Biostatistics Unit, Faculty of Health, Deakin University, Burwood, VIC, Australia | [d] Department of Medicine-Western Health, The University of Melbourne, St Albans, VIC, Australia | [e] Department of Epidemiology and Preventive Medicine, Monash University, Prahran, VIC, Australia | [f] Barwon Health, Geelong, VIC, Australia | [g] Department of Geriatric Medicine, Barwon Health, Geelong, VIC, Australia
Correspondence: [*] Correspondence to: Veer Bala Gupta, Deakin University, IMPACT – The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Geelong, VIC 3216, Australia. E-mail: veer.gupta@deakin.edu.au.
Abstract: Background:Poor cognitive function, a major disabling condition of older age, is often considered a prodromal feature of dementia. High mortality and the lack of a cure for dementia have necessitated a focus on the identification of potentially modifiable risk factors. Mental and physical health conditions such as mood disorders and bone loss have been previously linked with poor cognition individually although their combined effect remains largely unknown. Objective:Considering the multifactorial nature of dementia pathology, we investigated whether mood disorders, bone health and their interaction are associated with cognitive function in a population-based sample of men. Methods:Four hundred and forty-two male participants were drawn from the Geelong Osteoporosis Study. Cognitive function was assessed using the CogState Brief Battery, which measured cognitive performance across four domains and was used to compute overall cognitive function. Mood disorders and hip bone mineral density (BMD) were determined using a semi-structured clinical interview and dual-energy X-ray absorptiometry, respectively. Results:Hip BMD (Bcoeff = 0.56, 95% CI: [0.07, 1.05], p = 0.025) but not mood disorder (Bcoeff = –0.50, 95% CI: [–0.20, 0.10], p = 0.529) was associated with overall cognitive function after accounting for potential confounders. Interaction effects were observed between the two exposures (Bcoeff = –1.37, 95% CI: [–2.49, –0.26], p = 0.016) suggesting that individuals without a mood disorder displayed better cognitive performance with increasing BMD, while those with a lifetime history of mood disorder displayed poorer cognitive function with increasing BMD. Conclusions:These findings highlight the importance of exploring interactions among potentially modifiable health conditions associated with cognitive function.
Keywords: Alzheimer’s disease, bone mineral density, cognitive function, interaction, mood disorder
DOI: 10.3233/JAD-230140
Journal: Journal of Alzheimer's Disease, vol. 96, no. 1, pp. 381-393, 2023
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
sales@iospress.com
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
info@iospress.nl
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office info@iospress.nl
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
china@iospress.cn
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
如果您在出版方面需要帮助或有任何建, 件至: editorial@iospress.nl