Interactions Between Age, Sex, Menopause, and Brain Structure at Midlife: A UK Biobank Study

Author:

Than Stephanie12ORCID,Moran Chris12,Beare Richard13,Vincent Amanda J45,Collyer Taya A1,Wang Wei16,Callisaya Michele L17,Thomson Russell8,Phan Thanh G9,Fornito Alex10,Srikanth Velandai K12

Affiliation:

1. Academic Unit, Peninsula Clinical School, Central Clinical School, Melbourne, Monash University, Victoria, Australia

2. Department of Geriatric Medicine, Peninsula Health, Melbourne, Victoria, Australia

3. Developmental Imaging, Murdoch Children’s Research Institute, Melbourne, Victoria, Australia

4. Monash Centre for Health Research and Implementation, School of Public Health and Preventative Medicine, Monash University, Melbourne, Victoria, Australia

5. Department of Endocrinology, Monash Health, Melbourne, Victoria, Australia

6. Department of Clinical Epidemiology, School of Public Health and Preventative Medicine, Cabrini Institute, Monash University, Melbourne, Victoria, Australia

7. Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia

8. Centre for Research in Mathematics, Western Sydney University, Sydney, New South Wales, Australia

9. Stroke and Aging Research Group, School of Clinical Sciences, Monash University, Melbourne, Victoria, Australia

10. Monash Biomedical Imaging, School of Psychological Science, Turner Institute for Brain and Mental Health, Monash University, Melbourne, Victoria, Australia

Abstract

Abstract Objectives Age and female sex are risk factors for dementia, and menopause is associated with cognitive dysfunction. Previous work largely considered the effects of sex and menopause as being independent of age. We studied whether age interacts with sex or menopause in explaining imaging biomarkers of dementia during midlife. Methods In this cross-sectional study of UK Biobank participants with brain magnetic resonance imaging (MRI), we explored the interaction of age with sex or menopausal status in explaining total brain volume (TBV), gray matter volume (GMV), white matter volume (WMV), white matter hyperintensity volume (WMHV), regional cortical volume , and subcortical volume. Results Data were available for 1827 postmenopausal women, 230 pre/perimenopausal women and 2165 men (median age 63.3 years). There was a significant interaction between age and sex (P = .024) for TBV, where the inverse association age with TBV was steeper in women (β = –5.35 mL/year) than in men (β = –4.77 mL/year). Similar age–sex interactions were also observed for GMV and WMV. In women, there was a significant interaction between age and menopausal status (P = .007) where the inverse association of age with TBV was steeper in postmenopausal (β = –5.89 mL/year) than in pre/perimenopausal women (β = –1.61 mL/year). Similar age–menopause interactions were found in predicting lower GMV and higher WMHV. Differences in the direction of these age–sex and age–menopause interactions were found for regional cortical and subcortical brain volumes. Conclusion Sex and menopause both interact with age during midlife in explaining MRI biomarkers of dementia. Further work is required to understand the mechanisms driving these interactions to develop strategies for delaying dementia.

Funder

National Health and Medical Research Council of Australia

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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