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Effects of peripheral vascular intervention on ischemia-modified albumin

Authors :
Stefan Förster
Esin Akcakoyunlu
Martin Reincke
Christian la Fougère
Reinhold Tiling
Hans X. Hoyer
Christof Weber
Christoph Schuhmann
Hae-Young Sohn
Marcus Hacker
Source :
Coronary Artery Disease. 18:375-379
Publication Year :
2007
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2007.

Abstract

Ischemia -modified albumin was regarded as an early marker of cardiac ischemia. On the other hand, it has been reported that increased ischemia-modified albumin levels are associated with unstable plaque processes like percutaneous coronary intervention, acute coronary syndrome or myocardial infarction. This prospective study aimed to investigate the role of ischemia-modified albumin in patients with peripheral vascular disease undergoing peripheral vascular intervention, a plaque-altering procedure without evidence of tissue ischemia. Peripheral vascular intervention was performed in 21 consecutive patients (68.2+/-13.3 years) with typical leg claudication and documented peripheral vascular disease. Additionally, 96 consecutive patients (66+/-12.0 years) undergoing routine exercise stress test for the exclusion of functionally relevant coronary artery disease were defined as controls. It was assumed that in the latter patients no unstable plaque-altering processes were present. Blood samples were drawn before, and 30 min and 3 h after, revascularization in the peripheral vascular intervention group, as well as before, and 30 min and 3 h after, maximum stress testing in the control group, respectively. Ischemia-modified albumin levels were analyzed using the albumin cobalt-binding test. In patients undergoing peripheral vascular intervention, ischemia-modified albumin increased from 116.6+/-19.1 U/ml at baseline to 132.0+/-19.3 U/ml 30 min after intervention (+14.4+/-15.7%, P

Details

ISSN :
09546928
Volume :
18
Database :
OpenAIRE
Journal :
Coronary Artery Disease
Accession number :
edsair.doi.dedup.....c668cbc2f8e4dce98dd41e425fac0c19
Full Text :
https://doi.org/10.1097/mca.0b013e3281ac2094