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. 2025 Jan;21(1):e14343.
doi: 10.1002/alz.14343. Epub 2024 Dec 22.

Sex and APOE ε4 allele differences in longitudinal white matter microstructure in multiple cohorts of aging and Alzheimer's disease

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Sex and APOE ε4 allele differences in longitudinal white matter microstructure in multiple cohorts of aging and Alzheimer's disease

Amalia Peterson et al. Alzheimers Dement. 2025 Jan.

Abstract

Introduction: The effects of sex and apolipoprotein E (APOE)-Alzheimer's disease (AD) risk factors-on white matter microstructure are not well characterized.

Methods: Diffusion magnetic resonance imaging data from nine well-established longitudinal cohorts of aging were free water (FW)-corrected and harmonized. This dataset included 4741 participants (age = 73.06 ± 9.75) with 9671 imaging sessions over time. FW and FW-corrected fractional anisotropy (FAFWcorr) were used to assess differences in white matter microstructure by sex and APOE ε4 carrier status.

Results: Sex differences in FAFWcorr in projection tracts and APOE ε4 differences in FW limbic and occipital transcallosal tracts were most pronounced.

Discussion: There are prominent differences in white matter microstructure by sex and APOE ε4 carrier status. This work adds to our understanding of disparities in AD. Additional work to understand the etiology of these differences is warranted.

Highlights: Sex and apolipoprotein E (APOE) ε4 carrier status relate to white matter microstructural integrity. Females generally have lower free water-corrected fractional anisotropy compared to males. APOE ε4 carriers tended to have higher free water than non-carriers.

Keywords: Alzheimer's disease; aging; sex differences; white matter disease.

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Conflict of interest statement

S.C.J. has served on advisory boards for Enigma Biomedical and ALZPath in the past 2 years. A.J.S. receives support from multiple NIH grants (P30 AG010133, P30 AG072976, R01 AG019771, R01 AG057739, U19 AG024904, R01 LM013463, R01 AG068193, T32 AG071444, U01 AG068057, U01 AG072177, U19 AG074879, and U24 AG074855). He has also received support from Avid Radiopharmaceuticals, a subsidiary of Eli Lilly (in kind contribution of PET tracer precursor) and participated in scientific advisory boards (Bayer Oncology, Eisai, Novo Nordisk, and Siemens Medical Solutions USA, Inc) and an observational study monitoring board (MESA, NIH NHLBI), as well as external advisory committees for multiple NIA grants. He also serves as editor in chief of Brain Imaging and Behavior, a Springer‐Nature journal. B.A.L. serves as editor in chief of SPIE Journal of Medical Imaging. L.L.B. serves as deputy editor of Alzheimer's & Dementia. A.L.J. serves on the NINDS DIVERSE VCID and NINDS RECOVERY observational study monitoring boards. She serves on the scientific advisory committee for the Paul B. Beeson Emerging Leaders Career Development Program, American Federation for Aging Research. She serves on the Clin‐STAR Coordinating Center External Advisory Committee, the external advisory board for the Kansas Alzheimer's Disease Core Center, and the Alzheimer's Disease and Related Dementia Advisory Council. A.W.T. serves on the RHU‐SHIVA data safety monitoring board and the ADNI Steering Committee and Executive Committee and is a member of the World Dementia Council and the Alzheimer's Disease Initiative Global Technical Advisory Committee. T.J.H. serves on the scientific advisory board for Vivid Genomics. He serves as Alzheimer's & Dementia: TRCI deputy editor and the Alzheimer's & Dementia senior associate editor. J.E.W. received financial support from IONIS pharmaceuticals. A.P., A.S., D.Z., Y.Y., A.D., K.D.D., N.S., K.R.P., M.E.K., C.G., N.M.K., Z.L., T.Y., Y.K., L.D., K.A.G., F.E.C., S.L.R., L.L.B.H., Y.A., K.A., G.E., C.D., D.T., P.M.T., E.C.M., M.H., D.W., P.Z., K.S., M.A., W.K., S.A.B., J.S., D.A.B., S.M.R., D.B.A., ADNI, BIOCARD, and ADSP have no conflicts to disclose. The authors declare no conflicts of interest. Author disclosures are available in the supporting information.

Figures

FIGURE 1
FIGURE 1
Forty‐eight white matter tractography templates were used in the present study, and can be grouped into TC (A), association (B), projection (C), and limbic tracts (D). IFG, inferior frontal gyrus; IFOF, inferior fronto‐occipital fasciculus; ILF, inferior longitudinal fasciculus; IPL, inferior parietal lobe; M1, primary motor cortex; PMd, dorsal premotor; PMv, ventral premotor; S1, primary somatosensory cortex; SLF, superior longitudinal fasciculus; SLF‐TP, temporoparietal superior longitudinal fasciculus; SMA, supplementary motor area; SPL, superior parietal lobe; TC, transcallosal; UF, uncinate fasciculus.
FIGURE 2
FIGURE 2
The main effects of sex and APOE ε4 on change in white matter microstructure. Linear mixed effects regression was conducted to determine the association of sex and APOE ε4 positivity on change in FAFWcorr (A) and change in FW (B). For both measures, heatmaps are grouped by tract type and illustrate the test statistic (i.e., z value) for each independent regression analysis. The top sex and APOE ε4 associations for both measures are illustrated with spaghetti plots. *Tracts surviving correction for multiple comparisons. APOE, apolipoprotein E; CC, corpus callosum; FAFWcorr, free water‐corrected fractional anisotropy; FW, free water; IFG, inferior frontal gyrus; IFOF, inferior fronto‐occipital fasciculus; ILF, inferior longitudinal fasciculus; IPL, inferior parietal lobe; M1, primary motor cortex; PMd, dorsal premotor; PMv, ventral premotor; S1, primary somatosensory cortex; SLF, superior longitudinal fasciculus; SLF‐TP, temporoparietal superior longitudinal fasciculus; SMA, supplementary motor area; SPL, superior parietal lobe; TC, transcallosal; UF, uncinate fasciculus.
FIGURE 3
FIGURE 3
Aggregated tract‐type associations with changes in white matter microstructure. z values of individual tracts were grouped into the following tract types: association, limbic, projection, prefrontal TC, motor TC, parietal TC, and occipital TC for FAFWcorr (A) and FW (B). The left, middle, and right columns display the sex main effect (red), APOE ε4 main effect (blue), and sex × APOE ε4 interaction (orange), respectively. APOE, apolipoprotein E; FAFWcorr, free water–corrected fractional anisotropy; FW, free water; TC, transcallosal.

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