Generative adversarial network constrained multiple loss autoencoder: A deep learning-based individual atrophy detection for Alzheimer's disease and mild cognitive impairment

被引:19
作者
Shi, Rong [1 ]
Sheng, Can [2 ]
Jin, Shichen [1 ]
Zhang, Qi [1 ]
Zhang, Shuoyan [1 ]
Zhang, Liang
Ding, Changchang [1 ]
Wang, Luyao [1 ]
Wang, Lei [4 ]
Han, Ying [2 ,3 ,5 ,6 ,9 ]
Jiang, Jiehui [7 ,8 ]
机构
[1] Shanghai Univ, Sch Informat & Commun Engn, Shanghai, Peoples R China
[2] Xuanwu Hosp Capital Med Univ, Dept Neurol, Beijing, Peoples R China
[3] Hainan Univ, Sch Biomed Engn, Key Lab Biomed Engn Hainan Prov, Haikou, Peoples R China
[4] Drexel Univ, Coll Comp & Informat, Philadelphia, PA USA
[5] Beijing Inst Brain Disorders, Ctr Alzheimers Dis, Beijing, Peoples R China
[6] Natl Clin Res Ctr Geriatr Disorders, Beijing, Peoples R China
[7] Shanghai Univ, Inst Biomed Engn, Sch Life Sci, Shanghai, Peoples R China
[8] Shanghai Univ, Inst Biomed Engn, Sch Informat & Commun Engn, Shanghai 200444, Peoples R China
[9] Capital Med Univ, Dept Neurol, Xuanwu Hosp, Beijing 100053, Peoples R China
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
Alzheimer's disease; GAN; magnetic resonance imaging; precision medicine; MEDIAL TEMPORAL-LOBE; CORTICAL SIGNATURE; HIPPOCAMPAL; HETEROGENEITY; PERFORMANCE; BIOMARKER; DEMENTIA; PATTERNS; IMAGES; SHAPE;
D O I
10.1002/hbm.26146
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Exploring individual brain atrophy patterns is of great value in precision medicine for Alzheimer's disease (AD) and mild cognitive impairment (MCI). However, the current individual brain atrophy detection models are deficient. Here, we proposed a framework called generative adversarial network constrained multiple loss autoencoder (GANCMLAE) for precisely depicting individual atrophy patterns. The GANCMLAE model was trained using normal controls (NCs) from the Alzheimer's Disease Neuroimaging Initiative cohort, and the Xuanwu cohort was employed to validate the robustness of the model. The potential of the model for identifying different atrophy patterns of MCI subtypes was also assessed. Furthermore, the clinical application potential of the GANCMLAE model was investigated. The results showed that the model can achieve good image reconstruction performance on the structural similarity index measure (0.929 +/- 0.003), peak signal-to-noise ratio (31.04 +/- 0.09), and mean squared error (0.0014 +/- 0.0001) with less latent loss in the Xuanwu cohort. The individual atrophy patterns extracted from this model are more precise in reflecting the clinical symptoms of MCI subtypes. The individual atrophy patterns exhibit a better discriminative power in identifying patients with AD and MCI from NCs than those of the t-test model, with areas under the receiver operating characteristic curve of 0.867 (95%: 0.837-0.897) and 0.752 (95%: 0.71-0.790), respectively. Similar findings are also reported in the AD and MCI subgroups. In conclusion, the GANCMLAE model can serve as an effective tool for individualised atrophy detection.
引用
收藏
页码:1129 / 1146
页数:18
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