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Correlation between near-infrared Raman spectroscopy and the histopathological analysis of atherosclerosis in human coronary arteries

✍ Scribed by Landulfo Silveira Jr.; Sokki Sathaiah; Renato A. Zângaro; Marcos T. T. Pacheco; Maria C. Chavantes; Carlos A. G. Pasqualucci


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
129 KB
Volume
30
Category
Article
ISSN
0196-8092

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✦ Synopsis


Abstract

Background and Objectives

Modern diagnostic methods such as near‐infrared Raman spectroscopy (NIRS) allow quantification and evaluation of human atherosclerotic lesions, which can be useful in diagnosing coronary artery disease. The objective of the present study is to obtain feasible diagnostic information to detect atheromatous plaque using NIRS combined with discriminant analysis.

Study Design/Material and Methods

An 830 nm Ti: sapphire laser pumped by an argon laser provides near‐infrared excitation. A spectrograph disperses light scattered from arterial tissue and a liquid‐nitrogen cooled CCD detects the Raman spectra. A total of 111 arterial fragments were scanned and Raman results were compared with histopathology. Principal components analysis (PCA) and Mahalanobis distance (m‐distance) were used to model an algorithm for tissue classification into three categories: non‐atherosclerotic (NA), non‐calcified (NC), and calcified (C) using Raman spectra. Spectra were randomly separated into training and prospective groups.

Results

It has been found that, for the NA tissue, the algorithm has sensitivity of 84 and 78% and specificity of 91 and 93% for training and prospective groups, respectively. For the NC tissue the algorithm has sensitivity of 88 and 90% and specificity of 88 and 83%. For the C tissue both sensitivity and specificity were maximum, 100%.

Conclusions

An algorithm using PCA and discriminant analysis based on m‐distance has been developed and successfully applied to diagnose coronary artery disease by NIRS obtaining good sensitivity and specificity for each tissue category. Lasers Surg. Med. 30:290–297, 2002. © 2002 Wiley‐Liss, Inc.


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