TY - JOUR
T1 - Laguerre-based method for analysis of time-resolved fluorescence data
T2 - Application to in-vivo characterization and diagnosis of atherosclerotic lesions
AU - Jo, Javier A.
AU - Fang, Qiyin
AU - Papaioannou, Thanassis
AU - Baker, J. Dennis
AU - Dorafshar, Amir
AU - Reil, Todd
AU - Qiao, Jian Hua
AU - Fishbein, Michael C.
AU - Freischlag, Julie A.
AU - Marcu, Laura
N1 - Funding Information:
This work was supported by the National Institutes of Health grant R01 HL 67377.
PY - 2006/3
Y1 - 2006/3
N2 - 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.
AB - 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.
KW - Fluorescence spectroscopy
KW - Laguerre deconvolution
KW - Optical diagnosis
KW - Vulnerable atherosclerotic plaques
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U2 - 10.1117/1.2186045
DO - 10.1117/1.2186045
M3 - Article
C2 - 16674179
AN - SCOPUS:33746404371
SN - 1083-3668
VL - 11
JO - Journal of biomedical optics
JF - Journal of biomedical optics
IS - 2
M1 - 021004
ER -