4.5 Article

Sex differences in brain aging among adults with family history of Alzheimer's disease and APOE4 genetic risk

Journal

NEUROIMAGE-CLINICAL
Volume 30, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2021.102620

Keywords

Family history; APOE; Brain aging; Alzheimer's disease

Categories

Funding

  1. CIHR Sex and Gender Research Chair [GS9-171369, 201610PJT-153321]
  2. NSERC [RGPIN-2018-05761]
  3. Wilfred and Joyce Posluns Chair in Women's Brain Health and Aging (the Women's Brain Health Initiative)
  4. Wilfred and Joyce Posluns Chair in Women's Brain Health and Aging (Ontario Brain Institute)
  5. Wilfred and Joyce Posluns Chair in Women's Brain Health and Aging (Canadian Institutes of Health Research)
  6. Canadian Consortium on Neurodegeneration and Aging's Women, Sex, Gender, and Dementia Cross-Cutting Program
  7. Natural Science and Engineering Research Council Graham Bell Canada Graduate Scholarship-Doctoral
  8. Healthy Brains Healthy Lives Doctoral Fellowship
  9. McGill University
  10. Fonds de Recherche du Quebec - Sante
  11. Pfizer Canada
  12. Levesque Foundation
  13. Douglas Hospital Research Centre and Foundation
  14. Government of Canada
  15. Canada Fund for Innovation

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The study found that women with AD risk factors experience greater brain aging than men, and higher BMI may help reduce brain aging in women but not in men. Additionally, physical activity is more beneficial for men's brain aging than women's in those with certain risk factors.
Emerging evidence suggests that Alzheimer's Disease (AD) risk factors may differentially contribute to disease trajectory in women than men. Determining the effect of AD risk factors on brain aging in women, compared to men, is critical for understanding whether there are sex differences in the pathways towards AD in cognitively intact but at-risk adults. Brain Age Gap (BAG) is a concept used increasingly as a measure of brain health; BAG is defined as the difference between predicted age (based on structural MRI) and chronological age, with negative values reflecting preserved brain health with age. Using BAG, we investigated whether there were sex differences in the brain effects of AD risk factors (i.e., family history of AD, and carrying an apolipopmtein E epsilon 4 allele [+APOE4]) in cognitively intact adults, and if this relationship was moderated by modifiable factors (i.e. body mass index [BMI], blood pressure and physical activity). We undertook a cross-sectional study of structural MRIs from 1067 cognitively normal adults across four neuroimaging datasets. An elastic net regression model found that women with a family history of AD and +APOE4 genotype had more advanced brain aging than their male counterparts. In a sub-cohort of women with those risk factors, higher BMI was associated with less brain aging whereas lower BMI was not. In a sub-cohort of women and men with +APOE4, engaging in physical activity was more beneficial to men's brain aging than women's. Our results demonstrate that AD risk factors are associated with greater brain aging in women than men, although there may be more unexplored modifiable factors that influence this relationship. These findings suggest that the complex interplay between unmodifiable and modifiable AD risk factors can potentially protect against brain aging in women and men.

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