INCREASES IN SERUM UNBOUND FREE FATTY-ACID LEVELS FOLLOWING CORONARY ANGIOPLASTY

Citation
Am. Kleinfeld et al., INCREASES IN SERUM UNBOUND FREE FATTY-ACID LEVELS FOLLOWING CORONARY ANGIOPLASTY, The American journal of cardiology, 78(12), 1996, pp. 1350-1354
Citations number
23
Categorie Soggetti
Cardiac & Cardiovascular System
ISSN journal
00029149
Volume
78
Issue
12
Year of publication
1996
Pages
1350 - 1354
Database
ISI
SICI code
0002-9149(1996)78:12<1350:IISUFF>2.0.ZU;2-G
Abstract
Serum unbound free fatty acid levels (FFu) were measured in patients u ndergoing percutaneous transluminal coronary angioplasty (PTCA) using the fluorescent probe acrylodan intestinal fatty acid binding protein (ADIFAB). These ore the first measurements of FFA(u) under nonphysiolo gic conditions. In these studies, FFA(u) levels were determined in 22 patients 5 minutes before and 30 minutes after the procedure. Post-PTC A FFA(u) levels were higher than pre-PTCA levels in all patients. The average post-PTCA level for all patients was 103 nM, about 14-fold hig her than the 7.5 nM value observed in healthy subjects. Although all p atients exhibited elevated FFA(u) levels after PTCA, ischemic ST-segme nt changes were observed in only 11 of these patients. The average pos t-PTCA FFA(u) levels for patients with significant ST-segment changes (123 nM) were significantly higher than those in patients who did not exhibit such changes (47 nM). Average FFA(u) (22 nM) levels before the procedure were elevated in the patient population relative to healthy subjects and these values correlated positively with post-PTCA levels . These results suggest that increased serum FFA(u) levels reflect ang ioplasty-induced ischemia and that FFA(u) levels may provide a more se nsitive measure of ischemia than electrocardiographic measurements. Mo reover, because 30% of these patients had post-PTCA FFA(u) concentrati ons exceeding those found to alter in vitro cell function, the increas ed serum FFA(u) levels that accompany ischemia may be deleterious for myocardial function. (C) 1996 by Excerpta Medica, Inc.