Academic Unit, Peninsula Clinical School, Central Clinical School, Melbourne, Monash University, Victoria, Australia.
Department of Geriatric Medicine, Peninsula Health, Melbourne, Victoria, Australia.
J Clin Endocrinol Metab. 2021 Jan 23;106(2):410-420. doi: 10.1210/clinem/dgaa847.
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.
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.
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.
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.
年龄和性别是痴呆的危险因素,而绝经与认知功能障碍有关。以前的研究主要考虑了性别和绝经对年龄的独立影响。我们研究了在中年期间,年龄是否与性别或绝经相互作用来解释痴呆的影像学生物标志物。
在这项英国生物库参与者的脑磁共振成像(MRI)的横断面研究中,我们探讨了年龄与性别或绝经状态在解释总脑容量(TBV)、灰质体积(GMV)、白质体积(WMV)、白质高信号体积(WMHV)、区域皮质体积和皮质下体积方面的相互作用。
共有 1827 名绝经后妇女、230 名绝经前/围绝经期妇女和 2165 名男子(中位年龄 63.3 岁)的数据可用。TBV 存在年龄与性别之间的显著交互作用(P=0.024),TBV 与年龄的负相关在女性中更为陡峭(β=-5.35 毫升/年),而在男性中则较平缓(β=-4.77 毫升/年)。GMV 和 WMV 也观察到类似的年龄-性别相互作用。在女性中,年龄与绝经状态之间存在显著的交互作用(P=0.007),TBV 与年龄的负相关在绝经后妇女(β=-5.89 毫升/年)中比绝经前/围绝经期妇女(β=-1.61 毫升/年)更为陡峭。GMV 较低和 WMHV 较高也存在类似的年龄-绝经交互作用。在区域皮质和皮质下脑容量方面,发现这些年龄-性别和年龄-绝经相互作用的方向存在差异。
性别和绝经在中年期间都与年龄相互作用,解释痴呆的 MRI 生物标志物。需要进一步研究以了解驱动这些相互作用的机制,从而制定延迟痴呆的策略。