Identifying sex-specific risk architectures for predicting amyloid deposition using neural networks

被引:2
|
作者
Wang, Linghai [1 ,5 ]
Kolobaric, Antonija [1 ]
Aizenstein, Howard [1 ,2 ,3 ]
Lopresti, Brian [1 ]
Tudorascu, Dana [4 ]
Snitz, Beth [1 ]
Klunk, William [2 ,3 ]
Wu, Minjie [2 ]
机构
[1] Univ Pittsburgh, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Med, Pittsburgh, PA USA
[4] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA USA
[5] Geriatr Psychiat Neuroimaging Lab, Off 52017, UPMC Oxford Bldg,3501 Forbes Ave, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Small vessel disease; Machine learning; Beta-amyloid; Sex differences; WHITE-MATTER HYPERINTENSITIES; DISEASE; BETA; COGNITION; BURDEN;
D O I
10.1016/j.neuroimage.2023.120147
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In older adults without dementia, White Matter Hyperintensities (WMH) in MRI have been shown to be highly associated with cerebral amyloid deposition, measured by the Pittsburgh compound B (PiB) PET. However, the relation to age, sex, and education in explaining this association is not well understood. We use the voxel counts of regional WMH, age, one-hot encoded sex, and education to predict the regional PiB using a multilayer perceptron with only rectilinear activations using mean squared error. We then develop a novel, robust metric to understand the relevance of each input variable for prediction. Our observations indicate that sex is the most relevant pre-dictor of PiB and that WMH is not relevant for prediction. These results indicate that there is a sex-specific risk architecture for A beta deposition.
引用
收藏
页数:8
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