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    <subfield code="a">Praewphan Tocharoenkul  </subfield>
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    <subfield code="a">Pathum Thani, Thailand :</subfield>
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    <subfield code="a">A research study submitted in partial fulfillment of the requirements for the degree of Master of Engineering in Data Science and Artificial Intelligence, School of Engineering and Technology</subfield>
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    <subfield code="a">At present, there is no cure for Alzheimer{u2019}s disease. However, there are treatment  options for patients to have a better quality of life. Treatment makes use of acetyl cholinesterase inhibitorsto reduce destruction of the structures of the brain. It would be  very helpful if we can diagnose Alzheimer{u2019}s disease early and accurately. In the  literature, there are currently no models able to automatically classify abnormalities  related to Alzheimer{u2019}s disease in terms of severity level. I aim to develop a model able  to classify each lobe of the brain in term of severity. To achieve the aim, I performed three steps to developed models. Frist, I built a dataset  for training atrophy severity level classification models based on GCA assessment, then  I segmented the dataset according to the lobes of the brain. Finally, I aim to build a  model suitable for classifying each lobe of the brain in terms of severity. In the experiments, the models can classify the severity level for each lobe of brain.  The overall model obtained a test accuracy of 62.75%, broken down into the four  classes with frontal accuracy of 68.0%, parietal accuracy of 54.0%, a temporal accuracy  of 62.0%, and occipital accuracy of 67.0%. There are some limitations to the  experiments. First, I focused mainly on the axial view, which was recommended by Dr.  Dittapong in the initial studying stage. Because the dataset is complicated and sensitive  to label accurately, there may be discrepancies in the dataset. Due to the project time  limitations, I was unable to obtain substantial medical a training and knowledge. To  segment the dataset into each lobe of the brain, I picked a range of specific slices for  each lobe of the brain manually. Within the range I chose, there are some regions that  are not specific for the lobe, which may affect the accuracy of the model. From the model in this thesis, I further understand brain anatomy, especially the  structure of sulci and gyri, specific parts of the brain, limitations of the dataset, and how  to build the model to classify the severity level for each lobe of brain. In this thesis, I  developed an initial version of such a mode. While the result is not yet to be ready for  clinical utilization, it has laid some foundations for future research. </subfield>
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