4.6 Article

Sex Modulates the Pathological Aging Effect on Caudate Functional Connectivity in Mild Cognitive Impairment

期刊

FRONTIERS IN PSYCHIATRY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2022.804168

关键词

aging effect; caudate; mild cognitive impairment; functional connectivity; Alzheimer's Disease; sex difference

资金

  1. NIH [1RF1AG071566, COBRE 5P20GM109025]
  2. Cleveland Clinic Keep Memory Alive Young Investigator Award
  3. Women's Alzheimer's Movement
  4. Alzheimer's Disease Neuroimaging Initiative (ADNI
  5. National Institutes of Health) [U01 AG024904]
  6. DOD ADNI (Department of Defense) [W81XWH-12-2-0012]
  7. National Institute on Aging
  8. National Institute of Biomedical Imaging and Bioengineering
  9. ADNI clinical sites in Canada

向作者/读者索取更多资源

The purpose of this study was to assess the impact of pathological aging on caudate functional connectivity in individuals with mild cognitive impairment (MCI) and investigate the role of sex and amyloid in this process. The results showed that the MCI group had a significantly stronger age-related increase in caudate nodal strength compared to the cognitive normal (CN) group. The aging effect on caudate nodal strength was significant only for women with MCI, and the connectivity between the caudate and ventral prefrontal cortex played a substantial role in this aging effect. The study suggests that caudate nodal strength may serve as a sensitive biomarker of pathological aging in women with MCI.
PurposeTo assess the pathological aging effect on caudate functional connectivity among mild cognitive impairment (MCI) participants and examine whether and how sex and amyloid contribute to this process. Materials and MethodsTwo hundred and seventy-seven functional magnetic resonance imaging (fMRI) sessions from 163 cognitive normal (CN) older adults and 309 sessions from 139 participants with MCI were included as the main sample in our analysis. Pearson's correlation was used to characterize the functional connectivity (FC) between caudate nuclei and each brain region, then caudate nodal strength was computed to quantify the overall caudate FC strength. Association analysis between caudate nodal strength and age was carried out in MCI and CN separately using linear mixed effect (LME) model with covariates (education, handedness, sex, Apolipoprotein E4, and intra-subject effect). Analysis of covariance was conducted to investigate sex, amyloid status, and their interaction effects on aging with the fMRI data subset having amyloid status available. LME model was applied to women and men separately within MCI group to evaluate aging effects on caudate nodal strength and each region's connectivity with caudate nuclei. We then evaluated the roles of sex and amyloid status in the associations of neuropsychological scores with age or caudate nodal strength. An independent cohort was used to validate the sex-dependent aging effects in MCI. ResultsThe MCI group had significantly stronger age-related increase of caudate nodal strength compared to the CN group. Analyzing women and men separately revealed that the aging effect on caudate nodal strength among MCI participants was significant only for women (left: P = 6.23 x 10(-7), right: P = 3.37 x 10(-8)), but not for men (P > 0.3 for bilateral caudate nuclei). The aging effects on caudate nodal strength were not significantly mediated by brain amyloid burden. Caudate connectivity with ventral prefrontal cortex substantially contributed to the aging effect on caudate nodal strength in women with MCI. Higher caudate nodal strength is significantly related to worse cognitive performance in women but not in men with MCI. ConclusionSex modulates the pathological aging effects on caudate nodal strength in MCI regardless of amyloid status. Caudate nodal strength may be a sensitive biomarker of pathological aging in women with MCI.

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