Deep learning based neuronal soma detection and counting for Alzheimer's disease analysis. (May 2021)

• Record Type: Journal Article
• Authors: Li, Qiufu; Zhang, Yu; Liang, Hanbang; Gong, Hui; Jiang, Liang; Liu, Qiong; Shen, Linlin
• Is Part Of: Computer methods and programs in biomedicine. Volume 203(2021)
• Publication Date: 2021-05
• Subjects: Alzheimer's disease (AD) -- Micro-optical sectioning tomography (MOST) -- Brain region -- Neuronal soma -- Convolutional neural network (CNN) -- Deep learning; Medicine -- Computer programs -- Periodicals; Biology -- Computer programs -- Periodicals; Computers -- Periodicals; Medicine -- Periodicals; Médecine -- Logiciels -- Périodiques; Biologie -- Logiciels -- Périodiques; Biology -- Computer programs; Medicine -- Computer programs; Periodicals; Electronic journals; 610.28
• DOI: 10.1016/j.cmpb.2021.106023
• Languages: English
• ISSNs: 0169-2607

Abstract

Abstract: Background and objective: Alzheimer's Disease (AD) is associated with neuronal damage and decrease. Micro-Optical Sectioning Tomography (MOST) provides an approach to acquire high-resolution images for neuron analysis in the whole-brain. Application of this technique to AD mouse brain enables us to investigate neuron changes during the progression of AD pathology. However, how to deal with the huge amount of data becomes the bottleneck. Methods: Using MOST technology, we acquired 3D whole-brain images of six AD mice, and sampled the imaging data of four regions in each mouse brain for AD progression analysis. To count the number of neurons, we proposed a deep learning based method by detecting neuronal soma in the neuronal images. In our method, the neuronal images were first cut into small cubes, then a Convolutional Neural Network (CNN) classifier was designed to detect the neuronal soma by classifying the cubes into three categories, "soma", "fiber", and "background". Results: Compared with the manual method and currently available NeuroGPS software, our method demonstrates faster speed and higher accuracy in identifying neurons from the MOST images. By applying our method to various brain regions of 6-month-old and 12-month-old AD mice, we found that the amount of neurons in three brain regions (lateral entorhinal cortex, medial entorhinal cortex, and presubiculum) decreased slightly with the increase of age, which is consistent with the experimental results previously reported. Conclusion: This paper provides a new method to automatically handle the huge amounts of data and accurately identify neuronal soma from the MOST images. It also provides the potential possibility to construct a whole-brain neuron projection to reveal the impact of AD pathology on mouse brain.