A whole process interpretable and multi-modal deep reinforcement learning for diagnosis and analysis of Alzheimer's disease

Author(s):  
Quan Zhang ◽  
Qian Du ◽  
Guohua Liu

Abstract Objective Alzheimer's disease (AD), a common disease of the elderly with unknown etiology, has been bothering many people, especially with the aging of the population and the younger trend of this disease. Current AI methods based on individual information or magnetic resonance imaging (MRI) can solve the problem of diagnostic sensitivity and specificity, but still face the challenges of interpretability and clinical feasibility. In this study, we propose an interpretable multimodal deep reinforcement learning model for inferring pathological features and diagnosis of Alzheimer's disease. Approach First, for better clinical feasibility, the compressed-sensing MRI image is reconstructed by an interpretable deep reinforcement learning model. Then, the reconstructed MRI is input into the full convolution neural network to generate a pixel-level disease probability of risk map (DPM) of the whole brain for Alzheimer's disease. Finally, the DPM of important brain regions and individual information are input into the attention-based fully deep neural network to obtain the diagnosis results and analyze the biomarkers. 1349 multi-center samples were used to construct and test the model. Main Results Finally, the model obtained 99.6%±0.2, 97.9%±0.2, and 96.1%±0.3 area under curve (AUC) in ADNI, AIBL, and NACC, respectively. The model also provides an effective analysis of multimodal pathology and predicts the imaging biomarkers on MRI and the weight of each individual information. In this study, a deep reinforcement learning model was designed, which can not only accurately diagnose AD, but also analyze potential biomarkers. Significance In this study, a deep reinforcement learning model was designed. The model builds a bridge between clinical practice and artificial intelligence diagnosis and provides a viewpoint for the interpretability of artificial intelligence technology.

2021 ◽  
Vol 11 (4) ◽  
pp. 1574
Author(s):  
Shabana Urooj ◽  
Satya P. Singh ◽  
Areej Malibari ◽  
Fadwa Alrowais ◽  
Shaeen Kalathil

Effective and accurate diagnosis of Alzheimer’s disease (AD), as well as early-stage detection, has gained more and more attention in recent years. For AD classification, we propose a new hybrid method for early detection of Alzheimer’s disease (AD) using Polar Harmonic Transforms (PHT) and Self-adaptive Differential Evolution Wavelet Neural Network (SaDE-WNN). The orthogonal moments are used for feature extraction from the grey matter tissues of structural Magnetic Resonance Imaging (MRI) data. Irrelevant features are removed by the feature selection process through evaluating the in-class and among-class variance. In recent years, WNNs have gained attention in classification tasks; however, they suffer from the problem of initial parameter tuning, parameter setting. We proposed a WNN with the self-adaptation technique for controlling the Differential Evolution (DE) parameters, i.e., the mutation scale factor (F) and the cross-over rate (CR). Experimental results on the Alzheimer’s disease Neuroimaging Initiative (ADNI) database indicate that the proposed method yields the best overall classification results between AD and mild cognitive impairment (MCI) (93.7% accuracy, 86.0% sensitivity, 98.0% specificity, and 0.97 area under the curve (AUC)), MCI and healthy control (HC) (92.9% accuracy, 95.2% sensitivity, 88.9% specificity, and 0.98 AUC), and AD and HC (94.4% accuracy, 88.7% sensitivity, 98.9% specificity and 0.99 AUC).


Biomedicines ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 823
Author(s):  
Ekaterina A. Rudnitskaya ◽  
Tatiana A. Kozlova ◽  
Alena O. Burnyasheva ◽  
Natalia A. Stefanova ◽  
Nataliya G. Kolosova

Sporadic Alzheimer’s disease (AD) is a severe disorder of unknown etiology with no definite time frame of onset. Recent studies suggest that middle age is a critical period for the relevant pathological processes of AD. Nonetheless, sufficient data have accumulated supporting the hypothesis of “neurodevelopmental origin of neurodegenerative disorders”: prerequisites for neurodegeneration may occur during early brain development. Therefore, we investigated the development of the most AD-affected brain structures (hippocampus and prefrontal cortex) using an immunohistochemical approach in senescence-accelerated OXYS rats, which are considered a suitable model of the most common—sporadic—type of AD. We noticed an additional peak of neurogenesis, which coincides in time with the peak of apoptosis in the hippocampus of OXYS rats on postnatal day three. Besides, we showed signs of delayed migration of neurons to the prefrontal cortex as well as disturbances in astrocytic and microglial support of the hippocampus and prefrontal cortex during the first postnatal week. Altogether, our results point to dysmaturation during early development of the brain—especially insufficient glial support—as a possible “first hit” leading to neurodegenerative processes and AD pathology manifestation later in life.


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