Show simple item record

dc.contributor.advisorBai, Li
dc.creatorLi, Yiran
dc.date.accessioned2022-08-15T19:04:24Z
dc.date.available2022-08-15T19:04:24Z
dc.date.issued2022
dc.identifier.urihttp://hdl.handle.net/20.500.12613/8041
dc.description.abstractChemical exchange saturation transfer (CEST) magnetic resonance imaging (MRI) has emerged as a novel technology for precise diagnosis of various diseases using either endogenous molecules or exogenous administered contrast agents. CEST MRI methods rely on molecular signal saturation through radiofrequency pulses with the same frequency as a prescribed molecule (e.g., glutamate) to be measured in a magnetic field. Because the background signal from water modular is generally greater than the signal from the prescribed molecular by several orders of magnitude, there are many different types of molecules with similar magnetic frequency to be applied in CEST MRI. However, any offset from the desired frequency will produce large discrepancies due to the reduction of the background signal saturation. Current practice relies on acquiring extensive data at intentionally changed saturation frequencies and estimating the desired signal through data interpolation. This method is effective, but takes long acquisition time, making it impractical for clinical applications. To address this challenge, I developed CEST MRI methods to achieve the following two goals: 1) to accelerate the acquisition time; and 2) to increase the CEST contrast quantification quality. As the in-vivo MR environment is highly complicated and difficult to model accurately, I proposed to use deep learning (DL) to achieve these two goals. Three different methods are proposed to improve the procedure of CEST MRI: 1) a deep learning-based Glutamate CEST imaging B0-inhomogeneity correction method (DL-B0GluCEST) to accelerate the total scan time; 2) an improved DL-B0GluCEST method using data acquired from the downfield Z-spectrum only; 3) two deep learning-based methods for estimating B0 inhomogeneities from fewer calibration data. In contrast to currently practiced methods, my CEST methods are believing to be the first-of-its-kind CEST MRI methods utilizing deep learning approaches. More importantly, in my demonstrated applications, three proposed deep learning-based methods showed CEST contrast quantification quality improvement while significantly reducing CEST acquisition time by over 60%, 80%, and 80%, respectively.
dc.format.extent94 pages
dc.language.isoeng
dc.publisherTemple University. Libraries
dc.relation.ispartofTheses and Dissertations
dc.rightsIN COPYRIGHT- This Rights Statement can be used for an Item that is in copyright. Using this statement implies that the organization making this Item available has determined that the Item is in copyright and either is the rights-holder, has obtained permission from the rights-holder(s) to make their Work(s) available, or makes the Item available under an exception or limitation to copyright (including Fair Use) that entitles it to make the Item available.
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectElectrical engineering
dc.titleSIMULTANEOUS ARTIFACTS CORRECTION AND ACCELERATION FOR CHEMICAL EXCHANGE SATURATION TRANSFER IMAGING VIA DEEP LEARNING
dc.typeText
dc.type.genreThesis/Dissertation
dc.contributor.committeememberWang, Ze
dc.contributor.committeememberDu, Liang
dc.contributor.committeememberBiswas, Saroj K.
dc.contributor.committeememberErnst, Thomas
dc.description.departmentElectrical and Computer Engineering
dc.relation.doihttp://dx.doi.org/10.34944/dspace/8013
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.description.degreePh.D.
dc.identifier.proqst14969
dc.creator.orcid0000-0002-5502-2106
dc.date.updated2022-08-11T22:09:43Z
refterms.dateFOA2022-08-15T19:04:24Z
dc.identifier.filenameLi_temple_0225E_14969.pdf


Files in this item

Thumbnail
Name:
Li_temple_0225E_14969.pdf
Size:
2.662Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record