Abstract |
Accumulation of numerous macrophages in the fibrous cap is a key identifying feature of plaque inflammation and vulnerability. This study investigates the use of time-resolved laser-induced fluorescence spectroscopy (TR-LIFS) as a potential tool for detection of macrophage foam cells in the intima of atherosclerotic plaques. Experiments were conducted in vivo on 14 New Zealand rabbits (6 control, 8 hypercholesterolemic) following aortotomy to expose the intimal luminal surface of the aorta. Tissue autofluorescence was induced with a nitrogen pulse laser (337 nm, 1 ns). Lesions were histologically classified by the percent of collagen or macrophage foam cells as well as thickness of the intima. Using parameters derived from the time-resolved fluorescence emission of plaques, we determined that intima rich in macrophage foam cells can be distinguished from intima rich in collagen with high sensitivity (>85%) and specificity (>95%). This study demonstrates, for the first time, that a time-resolved fluorescence-based technique can differentiate and demark macrophage content versus collagen content in vivo. Our results suggest that TR-LIFS technique can be used in clinical applications for identification of inflammatory cells important in plaque formation and rupture.
|
Authors | Laura Marcu, Qiyin Fang, Javier A Jo, Thanassis Papaioannou, Amir Dorafshar, Todd Reil, Jian-Hua Qiao, J Dennis Baker, Julie A Freischlag, Michael C Fishbein |
Journal | Atherosclerosis
(Atherosclerosis)
Vol. 181
Issue 2
Pg. 295-303
(Aug 2005)
ISSN: 0021-9150 [Print] Ireland |
PMID | 16039283
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, P.H.S.)
|
Topics |
- Animals
- Atherosclerosis
(immunology, pathology)
- Disease Models, Animal
- Image Processing, Computer-Assisted
(instrumentation, methods)
- Lasers
- Macrophages
(pathology)
- Male
- Microscopy, Fluorescence
(instrumentation, methods)
- Rabbits
|