scholarly journals The Relationship between Gamma Glutamyl Transferase Levels and the Clinical Outcomes in Patients with ST-Segment Elevation Myocardial Infarction Undergoing Primary PCI

2013 ◽  
Vol 62 (18) ◽  
pp. C215 ◽  
Author(s):  
Mehmet Gül ◽  
Hüseyin Uyarel ◽  
Mehmet Ergelen ◽  
Ahmet Ekmekci ◽  
Ender Özal ◽  
...  
2007 ◽  
Vol 96 (8) ◽  
pp. 557-565 ◽  
Author(s):  
Volkhard Kurowski ◽  
Evangelos Giannitsis ◽  
Dirk P. Killermann ◽  
Uwe K. H. Wiegand ◽  
Ralph Toelg ◽  
...  

Author(s):  
Sujesh Kumar N. ◽  
Sajitha Krishnan

Background: Acute coronary syndrome (ACS) remains a leading cause of mortality and morbidity world-wide. Atherosclerosis is the predominant cause of ACS and biomarkers that could detect vulnerable atherosclerotic plaque could potentially be of great value in identifying patients at risk of developing coronary events. The aim was to assess the role of gamma-glutamyl transferase (GGT) in atherosclerosis process. The objective was to compare serum levels of GGT in patients with ACS and control subjects, and also to find out the association between GGT and atherogenic risk factors such as diabetes mellitus, hypertension, dyslipidemia and smoking.Methods: The design was a prospective case control study where a total of 151 patients, 100 ACS patients and 51 control subjects with the age group of 30-80 years were enrolled for the study. GGT was estimated by kinetic colour test using Beckman Coulter AU2700 analyser.Results: The mean GGT levels of ST-segment elevation myocardial infarction (STEMI), non-ST-segment elevation myocardial infarction (NSTEMI) and unstable angina (UA) subgroups were 93.86, 87.87 and 29.27 U/L respectively, which showed statistical significant difference (p<0.001) when compared with control subjects 21.99 U/L. The higher GGT levels in ACS patients also correlated with angiographic diagnosis of atherosclerosis. No significant difference was noted in GGT levels among ACS subgroups having risk factors and without having risk factors. Conclusions: Significantly higher GGT levels found in ACS patients reflects the burden of atherosclerotic changes and this association implies that GGT estimation can be used as an adjuvant biomarker that may help in identifying patients who are potentially at risk of coronary atherosclerosis.


2019 ◽  
Vol 40 (Supplement_1) ◽  
Author(s):  
A Karathanos ◽  
Y F Lin ◽  
L Dannenberg ◽  
C Parco ◽  
V Schulze ◽  
...  

Abstract Background Cardiovascular guidelines recommend adjunct glycoprotein IIb/IIIa inhibitors (GPI) only in selected patients with acute ST-segment elevation myocardial infarction (STEMI). Purpose This study aimed to evaluate routine GPI use in STEMI treated with primary PCI. Methods Online databases were systematically searched for randomised controlled trials (RCTs) of routine GPI vs. control therapy in STEMI. Data from retrieved studies were abstracted and evaluated in a comprehensive meta-analysis using Mantel-Haenszel estimates of risk ratios (RR) as summary statistics. Results After systematic review, twenty-one RCTs with 8,585 patients were included: ten trials randomized tirofiban (T), nine abciximab (A), one eptifibatide (E), one trial used A+T; only one trial used DAPT with prasugrel/ ticagrelor. Routine GPI were associated with a significant reduction in all-cause mortality at 30 days (2.4% (GPI) vs. 3.2%; risk ratio (RR) 0.72; p=0.01) and 6 months (3.7% vs. 4.8%; RR 0.76; p=0.02), and a reduction in recurrent MI (1.1% vs. 2.1%; RR 0.55; p=0.0006), repeat revascularization (2.5% vs. 4.1%; RR 0.63; p=0.0001), TIMI flow <3 after PCI (5.4% vs. 8.2%; RR 0.61; p<0.0001) and ischemic stroke (RR 0.42; p=0.04). Major (4.7% vs. 3.4%; RR 1.35; p=0.005) and minor bleedings (7.2% vs. 5.1%; RR 1.39; p=0.006) but not intracranial bleedings (0.1% vs. 0%; RR 2.7; p=0.37) were significantly increased under routine GPI. Conclusions Routine GPI administration during primary PCI in STEMI resulted in mortality reduction, driven by reductions in recurrent ischemic events – however predominantly in trials pre-prasugrel/ticagrelor. Trials in contemporary STEMI management are needed to confirm these findings.


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