Differential Role for Hippocampal Subfields in Alzheimer's Disease Progression Revealed with Deep Learning

被引:24
|
作者
Kwak, Kichang [1 ]
Niethammer, Marc [1 ,2 ]
Giovanello, Kelly S. [1 ,3 ]
Styner, Martin [2 ,4 ]
Dayan, Eran [1 ,5 ]
机构
[1] Univ N Carolina, Biomed Res Imaging Ctr, Chapel Hill, NC 27515 USA
[2] Univ N Carolina, Dept Comp Sci, Chapel Hill, NC 27515 USA
[3] Univ N Carolina, Dept Psychol & Neurosci, Chapel Hill, NC 27515 USA
[4] Univ N Carolina, Dept Psychiat, Chapel Hill, NC 27515 USA
[5] Univ N Carolina, Dept Radiol, Chapel Hill, NC 27515 USA
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
Alzheimer's disease; cognitive decline; deep learning; hippocampus; mild cognitive impairment; MILD COGNITIVE IMPAIRMENT; MRI; CONVERSION; ATROPHY; VOLUME; VIVO; SEGMENTATION; RELIABILITY; DEMENTIA; ROBUST;
D O I
10.1093/cercor/bhab223
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mild cognitive impairment (MCI) is often considered the precursor of Alzheimer's disease. However, MCI is associated with substantially variable progression rates, which are not well understood. Attempts to identify the mechanisms that underlie MCI progression have often focused on the hippocampus but have mostly overlooked its intricate structure and subdivisions. Here, we utilized deep learning to delineate the contribution of hippocampal subfields to MCI progression. We propose a dense convolutional neural network architecture that differentiates stable and progressive MCI based on hippocampal morphometry with an accuracy of 75.85%. A novel implementation of occlusion analysis revealed marked differences in the contribution of hippocampal subfields to the performance of the model, with presubiculum, CA1, subiculum, and molecular layer showing the most central role. Moreover, the analysis reveals that 10.5% of the volume of the hippocampus was redundant in the differentiation between stable and progressive MCI.
引用
收藏
页码:467 / 478
页数:12
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