<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-20T05:00:52Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/162692" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/162692</identifier><datestamp>2025-09-19T04:49:07Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131023</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Szolovits, Peter</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Li, Jonathan</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2025-09-18T14:27:36Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2025-09-18T14:27:36Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2025-05</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="submitted">2025-06-23T14:02:50.246Z</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1721.1/162692</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">This work focuses on the progression from metabolic dysfunction-associated fatty liver to metabolic dysfunction-associated steatohepatitis, a more serious prognosis that can lead to liver failure and death. Additional adverse progressed outcomes include hepatic failure, fibrosis, cirrhosis, and malignant neoplasm of liver and intrahepatic bile ducts. We explore the possibility of using different machine learning techniques, including logistic regression, XGBoost, random forest, and decision trees to predict the likelihood of progression. We use data from Massachusetts General Brigham to train our models, incorporating demographics, physical measurements, lab results, and doctor notes. As a result of this project, we our best model was an XGBoost classifier with an AUROC of 0.800 with random forest at a similar performance of 0.786. However, all of our models had low AUPRC and sensitivity, indicating both overfitting and an imbalanced dataset.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree">M.Eng.</dim:field>
   <dim:field mdschema="dc" element="publisher">Massachusetts Institute of Technology</dim:field>
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   <dim:field mdschema="dc" element="title">Predicting Progression of Metabolic Dysfunction-associated Steatotic Liver Disease</dim:field>
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   <dim:field mdschema="thesis" element="degree" qualifier="name">Master of Engineering in Electrical Engineering and Computer Science</dim:field>
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   	&lt;Title>Predicting Progression of Metabolic Dysfunction-associated Steatotic Liver Disease&lt;/Title>
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   	&lt;PublicationDate>2025-05&lt;/PublicationDate>
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        	&lt;DisplayName>Li, Jonathan&lt;/DisplayName>
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            &lt;DisplayName>Massachusetts Institute of Technology&lt;/DisplayName>
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   	&lt;Abstract>This work focuses on the progression from metabolic dysfunction-associated fatty liver to metabolic dysfunction-associated steatohepatitis, a more serious prognosis that can lead to liver failure and death. Additional adverse progressed outcomes include hepatic failure, fibrosis, cirrhosis, and malignant neoplasm of liver and intrahepatic bile ducts. We explore the possibility of using different machine learning techniques, including logistic regression, XGBoost, random forest, and decision trees to predict the likelihood of progression. We use data from Massachusetts General Brigham to train our models, incorporating demographics, physical measurements, lab results, and doctor notes. As a result of this project, we our best model was an XGBoost classifier with an AUROC of 0.800 with random forest at a similar performance of 0.786. However, all of our models had low AUPRC and sensitivity, indicating both overfitting and an imbalanced dataset.&lt;/Abstract>
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