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dc.contributor.authorFitzmaurice, Maryann
dc.contributor.authorGardecki, Joseph A.
dc.contributor.authorAngheloiu, George O.
dc.contributor.authorAwasthi, Samir
dc.contributor.authorMotz, Jason T.
dc.contributor.authorKramer, John R.
dc.contributor.authorFeld, Michael S.
dc.contributor.authorScepanovic, Obrad R.
dc.contributor.authorDasari, Ramachandra Rao
dc.date.accessioned2014-06-05T17:01:47Z
dc.date.available2014-06-05T17:01:47Z
dc.date.issued2006-03
dc.date.submitted2005-11
dc.identifier.issn10833668
dc.identifier.issn1560-2281
dc.identifier.urihttp://hdl.handle.net/1721.1/87654
dc.description.abstractVulnerable plaques, which are responsible for most acute ischemic events, are presently invisible to x-ray angiography. Their primary morphological features include a thin or ulcerated fibrous cap, a large necrotic core, superficial foam cells, and intraplaque hemorrhage. We present evidence that multimodal spectroscopy (MMS), a novel method that combines diffuse reflectance spectroscopy (DRS), intrinsic fluorescence spectroscopy (IFS), and Raman spectroscopy (RS), can detect these markers of plaque vulnerability. To test this concept, we perform an MMS feasibility study on 17 human carotid artery specimens. Following the acquisition of spectra, each specimen is histologically evaluated. Two parameters from DRS, hemoglobin concentration and a scattering parameter, are used to detect intraplaque hemorrhage and foam cells; an IFS parameter that relates to the amount of collagen in the topmost layers of the tissue is used to detect the presence of a thin fibrous cap; and an RS parameter related to the amount of cholesterol and necrotic material is used to detect necrotic core. Taken together, these spectral parameters can generally identify the vulnerable plaques. The results indicate that MMS provides depth-sensitive and complementary morphological information about plaque composition. A prospective in vivo study will be conducted to validate these findings.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01-HL-64675)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant P41-RR-02594)en_US
dc.language.isoen_US
dc.publisherSPIEen_US
dc.relation.isversionofhttp://dx.doi.org/10.1117/1.2187943en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSPIEen_US
dc.titleDetection of morphological markers of vulnerable atherosclerotic plaque using multimodal spectroscopyen_US
dc.typeArticleen_US
dc.identifier.citationScepanovic, Obrad R., Maryann Fitzmaurice, Joseph A. Gardecki, George O. Angheloiu, Samir Awasthi, Jason T. Motz, John R. Kramer, Ramachandra R. Dasari, and Michael S. Feld. “Detection of Morphological Markers of Vulnerable Atherosclerotic Plaque Using Multimodal Spectroscopy.” Journal of Biomedical Optics 11, no. 2 (2006): 021007. © 2006 Society of Photo-Optical Instrumentation Engineersen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physicsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Spectroscopy Laboratoryen_US
dc.contributor.mitauthorScepanovic, Obrad R.en_US
dc.contributor.mitauthorGardecki, Joseph A.en_US
dc.contributor.mitauthorAngheloiu, George O.en_US
dc.contributor.mitauthorAwasthi, Samiren_US
dc.contributor.mitauthorKramer, John R.en_US
dc.contributor.mitauthorDasari, Ramachandra Raoen_US
dc.contributor.mitauthorFeld, Michael S.en_US
dc.relation.journalJournal of Biomedical Opticsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsScepanovic, Obrad R.; Fitzmaurice, Maryann; Gardecki, Joseph A.; Angheloiu, George O.; Awasthi, Samir; Motz, Jason T.; Kramer, John R.; Dasari, Ramachandra R.; Feld, Michael S.en_US
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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