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患阿尔茨海默病风险的中年个体的白质微观和宏观结构特性:与性别和绝经状态的关联

White matter micro- and macrostructural properties in midlife individuals at risk for Alzheimer's disease: Associations with sex and menopausal status.

作者信息

Raikes Adam C, Dyke Jonathan P, Nerattini Matilde, Boneu Camila, Ajila Trisha, Fauci Francesca, Battista Michael, Pahlajani Silky, Williams Schantel, Brinton Roberta Diaz, Mosconi Lisa

机构信息

Center for Innovation in Brain Science, University of Arizona, Tucson, Arizona 85719.

Department of Radiology, Weill Cornell Medicine, New York, New York 10021.

出版信息

bioRxiv. 2025 Jun 13:2025.06.09.658686. doi: 10.1101/2025.06.09.658686.


DOI:10.1101/2025.06.09.658686
PMID:40661344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12259052/
Abstract

Women are at greater lifetime risk for Alzheimer's disease (AD), potentially due to midlife fractional anisotropy (FA) and lower mean diffusivity in fornix and corpus callosum, indicating more densely organized white matter. Perimenopausal women were the exception, with white matter profiles closely resembling those of men. Perimenopausal women exhibited minimal or absent fiber cross-section and FDC sex differences and a reversal of the fornix FA advantage observed in pre- and postmenopausal women. These cross-sectional results are consistent with sex differences in white matter organization. Importantly, the perimenopause emerges as a critical window of neural reorganization in the female midlife aging brain characterized by temporary convergence toward male-like white matter organization. Longitudinal analyses are key to identifying women who do or do not revert to a premenopausal profile, which may inform AD risk.

摘要

女性患阿尔茨海默病(AD)的终生风险更高,这可能是由于中年时穹窿和胼胝体的分数各向异性(FA)以及较低的平均扩散率,表明白质组织更密集。围绝经期女性是个例外,她们的白质特征与男性非常相似。围绝经期女性的纤维横截面和FDC性别差异最小或不存在,并且在绝经前和绝经后女性中观察到的穹窿FA优势出现了逆转。这些横断面结果与白质组织的性别差异一致。重要的是,围绝经期成为女性中年衰老大脑神经重组的关键窗口,其特征是暂时向男性样白质组织趋同。纵向分析对于识别是否恢复到绝经前状态的女性至关重要,这可能有助于了解AD风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/2483d78f18c8/nihpp-2025.06.09.658686v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/d279a5108526/nihpp-2025.06.09.658686v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/3e4cbf391ca7/nihpp-2025.06.09.658686v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/1276321c1adf/nihpp-2025.06.09.658686v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/2483d78f18c8/nihpp-2025.06.09.658686v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/d279a5108526/nihpp-2025.06.09.658686v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/3e4cbf391ca7/nihpp-2025.06.09.658686v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/1276321c1adf/nihpp-2025.06.09.658686v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5e/12259052/2483d78f18c8/nihpp-2025.06.09.658686v1-f0004.jpg

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White matter micro- and macrostructural properties in midlife individuals at risk for Alzheimer's disease: Associations with sex and menopausal status.

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本文引用的文献

[1]
Sources of information waste in neuroimaging: mishandling structures, thinking dichotomously, and over-reducing data.

Apert Neuro. 2022

[2]
Neurophysiological correlates of subjective cognitive decline in perimenopausal and postmenopausal midlife women at risk for Alzheimer's disease.

Menopause. 2025-5-1

[3]
How fiber bundle alterations differ in presumed LATE and amnestic Alzheimer's disease.

Alzheimers Dement. 2024-10

[4]
CAT: a computational anatomy toolbox for the analysis of structural MRI data.

Gigascience. 2024-1-2

[5]
Menstrual cycle-driven hormone concentrations co-fluctuate with white and gray matter architecture changes across the whole brain.

Hum Brain Mapp. 2024-8-1

[6]
Sex-related variability of white matter tracts in the whole HCP cohort.

Brain Struct Funct. 2024-9

[7]
In vivo brain estrogen receptor density by neuroendocrine aging and relationships with cognition and symptomatology.

Sci Rep. 2024-6-20

[8]
Fixel-Based Analysis Reveals Tau-Related White Matter Changes in Early Stages of Alzheimer's Disease.

J Neurosci. 2024-5-1

[9]
Sex-specific associations of serum cortisol with brain biomarkers of Alzheimer's risk.

Sci Rep. 2024-3-6

[10]
Systematic review and meta-analysis of the effects of menopause hormone therapy on risk of Alzheimer's disease and dementia.

Front Aging Neurosci. 2023-10-23

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