Effect of sex on the APOE4-aging interaction in the white matter microstructure of cognitively normal older adults using diffusion-tensor MRI with orthogonal-tensor decomposition (DT-DOME)

被引:1
|
作者
Srisaikaew, Patcharaporn [1 ,2 ]
Chad, Jordan A. [3 ,4 ]
Mahakkanukrauh, Pasuk [2 ,5 ]
Anderson, Nicole D. [3 ,6 ]
Chen, J. Jean [3 ,4 ,7 ]
机构
[1] Chiang Mai Univ, Fac Med, PhD Program Anat, Chiang Mai, Thailand
[2] Chiang Mai Univ, Fac Med, Dept Anat, Chiang Mai, Thailand
[3] Baycrest Hlth Sci, Rotman Res Inst, Toronto, ON, Canada
[4] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[5] Chiang Mai Univ, Excellence Osteol Res & Training Ctr, Chiang Mai, Thailand
[6] Univ Toronto, Dept Psychol & Psychiat, Toronto, ON, Canada
[7] Univ Toronto, Inst Biomed Engn, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
apolipoprotein E4 gene; cognitively normal older adults; diffusion tensor imaging (DTI); tensor decomposition; white matter (WM); sex effects; mode of anisotropy (MO); norm of anisotropy (NA); APOLIPOPROTEIN-E GENOTYPE; APOE EPSILON-4 ALLELE; ALZHEIMERS-DISEASE; RISK-FACTORS; INTEGRITY; BRAIN; AGE; CARRIERS; GENDER; INTERVENTION;
D O I
10.3389/fnins.2023.1049609
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The influence of the apolipoprotein E epsilon 4 allele (APOE4) on brain microstructure of cognitively normal older adults remains incompletely understood, in part due to heterogeneity within study populations. In this study, we examined white-matter microstructural integrity in cognitively normal older adults as a function of APOE4 carrier status using conventional diffusion-tensor imaging (DTI) and the novel orthogonal-tensor decomposition (DT-DOME), accounting for the effects of age and sex. Age associations with white-matter microstructure did not significantly depend on APOE4 status, but did differ between sexes, emphasizing the importance of accounting for sex differences in APOE research. Moreover, we found the DT-DOME to be more sensitive than conventional DTI metrics to such age-related and sex effects, especially in crossing WM fiber regions, and suggest their use in further investigation of white matter microstructure across the life span in health and disease.
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页数:13
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