Title
Laguerre-based method for analysis of time-resolved fluorescence data: Application to in-vivo characterization and diagnosis of atherosclerotic lesions
Date Issued
01 March 2006
Access level
open access
Resource Type
journal article
Author(s)
Fang Q.
Papaioannou T.
Baker J.D.
Dorafshar A.H.
Reil T.
Qiao J.H.
Fishbein M.C.
Freischlag J.A.
Marcu L.
University of California
Abstract
We report the application of the Laguerre deconvolution technique (LDT) to the analysis of in-vivo time-resolved laser-induced fluorescence spectroscopy (TR-LIFS) data and the diagnosis of atherosclerotic plaques. TR-LIFS measurements were obtained in vivo from normal and atherosclerotic aortas (eight rabbits, 73 areas), and subsequently analyzed using LDT. Spectral and time-resolved features were used to develop four classification algorithms: linear discriminant analysis (LDA), stepwise LDA (SLDA), principal component analysis (PCA), and artificial neural network (ANN). Accurate deconvolution of TR-LIFS in-vivo measurements from normal and atherosclerotic arteries was provided by LDT. The derived Laguerre expansion coefficients reflected changes in the arterial biochemical composition, and provided a means to discriminate lesions rich in macrophages with high sensitivity (>85%) and specificity (>95%). Classification algorithms (SLDA and PCA) using a selected number of features with maximum discriminating power provided the best performance. This study demonstrates the potential of the LDT for in-vivo tissue diagnosis, and specifically for the detection of macrophages infiltration in atherosclerotic lesions, a key marker of plaque vulnerability. © 2006 Society of Photo-Optical Instrumentation Engineers.
Volume
11
Issue
2
Language
English
OCDE Knowledge area
Tecnologías que implican la manipulación de células, tejidos, órganos o todo el organismo
Subjects
Scopus EID
2-s2.0-33746404371
PubMed ID
Source
Journal of Biomedical Optics
ISSN of the container
10833668
Sponsor(s)
This work was supported by the National Institutes of Health grant R01 HL 67377.
Sources of information:
Directorio de Producción Científica
Scopus