4.6 Article

Relationship of sex differences in cortical thickness and memory among cognitively healthy subjects and individuals with mild cognitive impairment and Alzheimer disease

期刊

ALZHEIMERS RESEARCH & THERAPY
卷 14, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13195-022-00973-1

关键词

Alzheimer Disease Dementia; Mild cognitive impairment; Sex; Magnetic resonance imaging; Cortical thickness; Memory; RAVLT; Machine learning

资金

  1. National Institute of General Medical Sciences of the National Institutes of Health [5P20GM109025]
  2. Nevada Exploratory Alzheimer's Disease Research Center (NVeADRC) [P20-AG068053]
  3. Women's Alzheimer's Movement/Maria Shriver
  4. Peter and Angela Dal Pezzo funds
  5. NINDS [U01NS093334]
  6. NIA [R01AG053798, R35AG71476]
  7. NIH [RF1-AG071566, R01-AG074392]
  8. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health) [U01 AG024904]
  9. DOD ADNI (Department of Defense) [W81XWH-12-2-0012]
  10. National Institute on Aging
  11. National Institute of Biomedical Imaging and Bioengineering
  12. AbbVie
  13. Alzheimer's Association
  14. Alzheimer's Drug Discovery Foundation
  15. Araclon Biotech
  16. BioClinica, Inc.
  17. Biogen
  18. Bristol-Myers Squibb Company
  19. CereSpir, Inc.
  20. Cogstate
  21. Eisai Inc.
  22. Elan Pharmaceuticals, Inc.
  23. Eli Lilly and Company
  24. EuroImmun
  25. F. Hoffmann-La Roche Ltd
  26. Genentech, Inc.
  27. Fujirebio
  28. GE Healthcare
  29. IXICO Ltd.
  30. Janssen Alzheimer Immunotherapy Research & Development, LLC.
  31. Johnson & Johnson Pharmaceutical Research & Development LLC.
  32. Lumosity
  33. Lundbeck
  34. Merck Co., Inc.
  35. Meso Scale Diagnostics, LLC.
  36. NeuroRx Research
  37. Neurotrack Technologies
  38. Novartis Pharmaceuticals Corporation
  39. Pfizer Inc.
  40. Piramal Imaging
  41. Servier
  42. Takeda Pharmaceutical Company
  43. Transition Therapeutics
  44. Canadian Institutes of Health Research
  45. Cleveland Clinic Lou Ruvo Center for Brain Health (Keep Memory Alive Foundation)

向作者/读者索取更多资源

This study, based on ADNI data, found that women have greater cortical thickness and better memory performance compared to men. Furthermore, differences in memory and cortical thickness between sexes may play a key role in the vulnerability and progression of ADD in women compared to men. Machine learning techniques showed that sex differences in cortical thickness are most relevant in the early stages of ADD neurodegeneration.
Background An aging society has increased rates of late onset Alzheimer disease dementia (ADD), the most common form of age-related dementia. This neurodegenerative disease disproportionately affects women. Methods We use data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) to examine sex differences in cortical thickness (CT) and memory performance. Analyses of covariance (ANCOVA) models were used to examine effects of sex and diagnosis (DX) on CT and verbal memory. For regions demonstrating significant interaction effects of sex and DX, we tested whether sex moderated cognition-thickness relationships. We used machine learning as a complementary method to explore multivariate CT differences between women and men. Results Women demonstrated greater CT in many brain regions. More specifically, men showed relatively consistent CT declines in all stages, from normal control (NC) to ADD in the bilateral cingulate cortex, bilateral temporal regions, and left precuneus; women had more stable CT in these regions between NC and mild cognitive impairment (MCI) stages, but sharper declines from MCI to ADD. Similarly, for the Rey Auditory Verbal Learning Test (RAVLT), ANCOVA analyses showed that women had significantly better immediate and delayed recall scores than men, at NC and MCI stages, but greater differences, cross-sectionally, from MCI to ADD than men. We found significant sex moderation effects between RAVLT-immediate scores and CT of right isthmus-cingulate for all subjects across DX. Partial correlation analyses revealed that increased CT of right isthmus-cingulate was associated with better verbal learning in women, driven by positron emission tomography defined amyloid positive (A beta+) subjects. Significant sex-moderation effects in cognition-thickness relationships were further found in the right middle-temporal, left precuneus, and left superior temporal regions in A beta+ subjects. Using a machine learning approach, we investigated multivariate CT differences between women and men, showing an accuracy in classification of 75% for A beta+ cognitively NC participants. Conclusions Sex differences in memory and CT can play a key role in the different vulnerability and progression of ADD in women compared to men. Machine learning indicates sex differences in CT are most relevant early in the ADD neurodegeneration.

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