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               <dc:title>Understanding Alzheimer’s disease progression through phenotypes discovery using manifold learning techniques</dc:title>
               <dc:creator>Pattarone, Natalia Karina</dc:creator>
               <dc:subject>MRI</dc:subject>
               <dc:subject>Imaging Techniques</dc:subject>
               <dc:subject>Alzheimer</dc:subject>
               <dc:subject>Manifolds</dc:subject>
               <dc:subject>Longitudinal Data</dc:subject>
               <dc:subject>Cross-sectional Data</dc:subject>
               <dc:description>Treball fi de màster de: Master in Intelligent Interactive Systems</dc:description>
               <dc:description>Tutor: Gemma Piella</dc:description>
               <dc:description>Alzheimer’s disease (AD) is clinically highly heterogeneous, varying in terms of&#xd;
rates of progression, test and cognitive symptoms among patients, as well as from&#xd;
a neuroimaging perspective. In the datasets provided by The Alzheimer’s Disease&#xd;
Neuroimaging Initiative (ADNI), researchers collect, validate and utilize data, including&#xd;
MRI and PET images, genetics, cognitive tests, CSF and blood biomarkers&#xd;
as predictors of the disease. Data coming from these datasets allow discovering&#xd;
phenotypes that could help to better understand the disease and provide targeted&#xd;
treatment.&#xd;
The objective of this thesis is to identify data-driven phenotypes using manifold&#xd;
learning and unsupervised clustering on multimodal longitudinal imaging and nonimaging&#xd;
data. First, we apply a novel approach for dimensionality reduction called&#xd;
PHATE that captures both local and global nonlinear structure using an informationgeometric&#xd;
distance between datapoints that would facilitate the discovery of possible&#xd;
AD phenotypes. Over PHATE output space, we performed a multiple-kernel unsupervised&#xd;
clustering to obtain profiles and describe AD phenotypes where features are&#xd;
weighted to construct kernels. Our results show that our approach can reveal AD&#xd;
progression trajectories in a lower dimensionality space, improving the results of the&#xd;
profiling where we obtained 4 possible profile subgroups using MRI cross-sectional&#xd;
baseline data and 8 possible profile subgroups when using longitudinal data. Furthermore,&#xd;
longitudinal data established clearer separation among profiles and higher&#xd;
significance for cognitive tests and general volumetric cerebral values than baseline&#xd;
data. Identifying these profiles could be useful for more personalized treatment of&#xd;
such a heterogeneous disease as AD.</dc:description>
               <dc:date>2021-12-20T11:47:03Z</dc:date>
               <dc:date>2021-12-20T11:47:03Z</dc:date>
               <dc:date>2021-07</dc:date>
               <dc:type>info:eu-repo/semantics/masterThesis</dc:type>
               <dc:rights>© Tots els drets reservats</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
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