<?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>2026-09-19T09:48:44Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/89990" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/89990</identifier><datestamp>2026-06-17T14:43:28Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</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" lang="en_US">Elfar AdalIsteinsson.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Fan, Audrey Peiwen</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science.</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">2014-09-19T21:32:59Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2014-09-19T21:32:59Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2014</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2014</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/89990</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">890131091</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Ph. D., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2014.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (pages 101-133).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The healthy brain consumes 20% of total oxygen used by the body under normal conditions. Continuous oxygen delivery to neural tissue is needed to maintain normal brain function and viability. Reliable measurements of brain oxygenation can provide critical information to diagnose and manage diseases in which this oxygen supply is disturbed, including stroke and tumor. In acute stroke, for instance, metabolic biomarkers such as local oxygen extraction fraction (OEF) have been shown to identify tissue at risk of infarction by positron emission tomography. This knowledge can then be used to identify patients who are candidates for reperfusion therapies or to avoid thrombolytic therapy in futile situations. Unfortunately, there is currently no clinically feasible method for radiologists to assess brain oxygenation in patients. My thesis aims to address this need through development of a clinically viable tool to examine regional OEF in the brain with magnetic resonance imaging (MRI). We have designed a novel imaging and analysis method to quantify oxygenation in cerebral veins. MRI phase images are sensitive to local, oxygenation-dependent magnetic field variations in brain vessels, due to the presence of paramagnetic deoxyhemoglobin molecules in venous blood. Our method was developed on a 3 Tesla MRI scanner and tested in 10 healthy volunteers during hypercapnia, i.e. breathing of low levels of CO₂. This respiratory challenge changes the baseline oxygenation state of the brain, enabling us to test whether our MRI method can detect different levels of OEF in vivo. We also show that OEF is reduced in 23 patients with multiple sclerosis, an autoimmune disease of the central nervous disease, and relates to their performance on cognitive tasks.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Audrey P. Fan.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">133 pages</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Electrical Engineering and Computer Science.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Development, testing, and application of quantitative oxygenation imaging from magnetic susceptibility by MRI</dim:field>
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   	&lt;Title>Development, testing, and application of quantitative oxygenation imaging from magnetic susceptibility by MRI&lt;/Title>
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   	&lt;PublicationDate>2014&lt;/PublicationDate>
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        	&lt;DisplayName>Fan, Audrey Peiwen&lt;/DisplayName>
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    &lt;Keyword>Electrical Engineering and Computer Science.&lt;/Keyword>
   	&lt;Abstract>The healthy brain consumes 20% of total oxygen used by the body under normal conditions. Continuous oxygen delivery to neural tissue is needed to maintain normal brain function and viability. Reliable measurements of brain oxygenation can provide critical information to diagnose and manage diseases in which this oxygen supply is disturbed, including stroke and tumor. In acute stroke, for instance, metabolic biomarkers such as local oxygen extraction fraction (OEF) have been shown to identify tissue at risk of infarction by positron emission tomography. This knowledge can then be used to identify patients who are candidates for reperfusion therapies or to avoid thrombolytic therapy in futile situations. Unfortunately, there is currently no clinically feasible method for radiologists to assess brain oxygenation in patients. My thesis aims to address this need through development of a clinically viable tool to examine regional OEF in the brain with magnetic resonance imaging (MRI). We have designed a novel imaging and analysis method to quantify oxygenation in cerebral veins. MRI phase images are sensitive to local, oxygenation-dependent magnetic field variations in brain vessels, due to the presence of paramagnetic deoxyhemoglobin molecules in venous blood. Our method was developed on a 3 Tesla MRI scanner and tested in 10 healthy volunteers during hypercapnia, i.e. breathing of low levels of CO₂. This respiratory challenge changes the baseline oxygenation state of the brain, enabling us to test whether our MRI method can detect different levels of OEF in vivo. We also show that OEF is reduced in 23 patients with multiple sclerosis, an autoimmune disease of the central nervous disease, and relates to their performance on cognitive tasks.&lt;/Abstract>
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