痴呆
神经影像学
疾病
弗雷明翰心脏研究
计算机科学
神经心理学
弗雷明翰风险评分
生物标志物
人口
深度学习
医学
阿尔茨海默病
人工智能
心理学
神经科学
认知
病理
生物化学
化学
环境卫生
作者
Shangran Qiu,Prajakta Joshi,Matthew I. Miller,Chonghua Xue,Xiao Zhou,Cody Karjadi,Gary H. Chang,Anant S. Joshi,Brigid Dwyer,Shuhan Zhu,Michelle Kaku,Yan Zhou,Yazan J. Alderazi,Arun Swaminathan,Sachin Kedar,Marie Saint‐Hilaire,Sanford Auerbach,Jing Yuan,E. Alton Sartor,Rhoda Au,Vijaya B. Kolachalama
出处
期刊:Brain
[Oxford University Press]
日期:2020-04-08
卷期号:143 (6): 1920-1933
被引量:280
标识
DOI:10.1093/brain/awaa137
摘要
Abstract Alzheimer’s disease is the primary cause of dementia worldwide, with an increasing morbidity burden that may outstrip diagnosis and management capacity as the population ages. Current methods integrate patient history, neuropsychological testing and MRI to identify likely cases, yet effective practices remain variably applied and lacking in sensitivity and specificity. Here we report an interpretable deep learning strategy that delineates unique Alzheimer’s disease signatures from multimodal inputs of MRI, age, gender, and Mini-Mental State Examination score. Our framework linked a fully convolutional network, which constructs high resolution maps of disease probability from local brain structure to a multilayer perceptron and generates precise, intuitive visualization of individual Alzheimer’s disease risk en route to accurate diagnosis. The model was trained using clinically diagnosed Alzheimer’s disease and cognitively normal subjects from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) dataset (n = 417) and validated on three independent cohorts: the Australian Imaging, Biomarker and Lifestyle Flagship Study of Ageing (AIBL) (n = 382), the Framingham Heart Study (n = 102), and the National Alzheimer’s Coordinating Center (NACC) (n = 582). Performance of the model that used the multimodal inputs was consistent across datasets, with mean area under curve values of 0.996, 0.974, 0.876 and 0.954 for the ADNI study, AIBL, Framingham Heart Study and NACC datasets, respectively. Moreover, our approach exceeded the diagnostic performance of a multi-institutional team of practicing neurologists (n = 11), and high-risk cerebral regions predicted by the model closely tracked post-mortem histopathological findings. This framework provides a clinically adaptable strategy for using routinely available imaging techniques such as MRI to generate nuanced neuroimaging signatures for Alzheimer’s disease diagnosis, as well as a generalizable approach for linking deep learning to pathophysiological processes in human disease.
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