TY - JOUR
T1 - New methods for time-resolved fluorescence spectroscopy data analysis based on the laguerre expansion technique
T2 - Applications in tissue diagnosis
AU - Jo, Javier A.
AU - Marcu, L.
AU - Fang, Q.
AU - Papaioannou, T.
AU - Qiao, J. H.
AU - Fishbein, M. C.
AU - Beseth, B.
AU - Dorafshar, A. H.
AU - Reil, T.
AU - Baker, D.
AU - Freischlag, J.
PY - 2007
Y1 - 2007
N2 - Objectives: A new deconvolution method for the analysis of time-resolved laser-induced fluorescence spectroscopy (TR-LIFS) data is introduced and applied for tissue diagnosis. Method: The intrinsic TR-LIFS decays are expanded on a Laguerre basis, and the computed Laguerre expansion coefficients (LEC) are used to characterize the sample fluorescence emission. The method was applied for the diagnosis of atherosclerotic vulnerable plaques. Results: At a first stage, using a rabbit atherosclerotic model, 73 TR-LIFS in-vivo measurements from the normal and atherosclerotic aorta segments of eight rabbits were taken. The Laguerre deconvolution technique was able to accurately deconvolve the TR-LIFS measurements. More interesting, the LEC reflected the changes in the arterial biochemical composition and provided discrimination of lesions rich in macrophages/foam-cells with high sensitivity (> 85%) and specificity (> 95%). At a second stage, 348 TR-LIFS measure-ments were obtained from the explanted carotid arteries of 30 patients. Lesions with significant inflammatory cells (macrophages/foam-cells and lymphocytes) were detected with high sensitivity (> 80%) and specificity (> 90%), using LEC-based classifiers. Conclusion: This study has demonstrated the potential of using TR-LIFS information by means of LEC for in-vivo tissue diagnosis, and specifically for detecting inflammation in atherosclerotic lesions, a key marker of plaque vulnerability.
AB - Objectives: A new deconvolution method for the analysis of time-resolved laser-induced fluorescence spectroscopy (TR-LIFS) data is introduced and applied for tissue diagnosis. Method: The intrinsic TR-LIFS decays are expanded on a Laguerre basis, and the computed Laguerre expansion coefficients (LEC) are used to characterize the sample fluorescence emission. The method was applied for the diagnosis of atherosclerotic vulnerable plaques. Results: At a first stage, using a rabbit atherosclerotic model, 73 TR-LIFS in-vivo measurements from the normal and atherosclerotic aorta segments of eight rabbits were taken. The Laguerre deconvolution technique was able to accurately deconvolve the TR-LIFS measurements. More interesting, the LEC reflected the changes in the arterial biochemical composition and provided discrimination of lesions rich in macrophages/foam-cells with high sensitivity (> 85%) and specificity (> 95%). At a second stage, 348 TR-LIFS measure-ments were obtained from the explanted carotid arteries of 30 patients. Lesions with significant inflammatory cells (macrophages/foam-cells and lymphocytes) were detected with high sensitivity (> 80%) and specificity (> 90%), using LEC-based classifiers. Conclusion: This study has demonstrated the potential of using TR-LIFS information by means of LEC for in-vivo tissue diagnosis, and specifically for detecting inflammation in atherosclerotic lesions, a key marker of plaque vulnerability.
KW - Atherosclerosis
KW - Laguerre deconvolution
KW - Time-resolved fluorescence spectroscopy
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U2 - 10.1055/s-0038-1625408
DO - 10.1055/s-0038-1625408
M3 - Article
C2 - 17347757
AN - SCOPUS:33947534859
SN - 0026-1270
VL - 46
SP - 206
EP - 211
JO - Methods of information in medicine
JF - Methods of information in medicine
IS - 2
ER -