Troponin levels in patients with stable CAD

Abstract Introduction Cardiac troponins are known as specific markers of myocardial damage. Their elevation in the serum is not always related to acute myocardial ischaemia. The increased sensitivity of diagnostic kits has resulted in an increase in the number of positive results in patients without...

Full description

Saved in:
Bibliographic Details
Published in:Cor et vasa (English ed.) Vol. 59; no. 3; pp. e229 - e234
Main Authors: Daněk, Josef, Hnátek, Tomáš, Malý, Martin, Táborský, Miloš, Běláček, Jaromír, Škvaril, Jan, Pospíšilová, Lenka, Černohous, Miroslav, Sedloň, Pavel, Hajšl, Martin, Zavoral, Miroslav
Format: Journal Article
Language:English
Published: Elsevier Urban & Partner Sp. z o.o 01-06-2017
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Abstract Introduction Cardiac troponins are known as specific markers of myocardial damage. Their elevation in the serum is not always related to acute myocardial ischaemia. The increased sensitivity of diagnostic kits has resulted in an increase in the number of positive results in patients without acute coronary syndrome (ACS). Study objectives To determine the level of highly sensitive troponin T (hs TnT) in stable patients (without ACS) before selective coronarography (SCG) and to determine the correlation between hs TnT values and the extent of atherosclerotic damage to the coronary arteries. Methodology We studied a group of 251 consecutive patients with indications for SCG diagnosis. Indication criteria were stable angina pectoris, shortness of breath, newly diagnosed heart failure, syncope, and ventricular arrhythmia. Exclusion criteria were acute coronary syndrome, including unstable angina pectoris, prior cardiopulmonary resuscitation, cerebrovascular accident (CVA) within the last 6 months, and ongoing sepsis. The hs TnT value was determined before SCG (normal range, 0–0.013 μg/l). Monitored parameters included coronary angiography (70% stenosis of coronary artery diameter was considered significant coronary disease), age, gender, heart rate, and serum creatinine levels. The study included 182 patients with normal renal function and 69 patients with renal insufficiency. The results were processed using STATISTICA (version 12), StatSoft©, Inc. (2013). Results The average age of the studied population was 69.6 ± 10.3 years (median, 70 years); 33% of patients were women. The serum level of hs TnT for the entire population was 0.031 ± 0.091 μg/l (0.014). A positive hs TnT was noted in 133 patients. The population study group consisted of 121 patients with normal coronary arteries or with insignificant atherosclerotic disease. Significant damage involving one or more arteries was present in 130 patients. In the subgroup with significant coronary disease, we found a significantly higher hs TnT level than in the group of patients without significant coronary disease: 0.043 ± 0.125 μg/l (0.018) vs. 0.019 ± 0.018 μg/l (0.013) ( p = 0.008) (Mann–Whitney test). Significantly higher troponin levels were found in the group of patients with renal insufficiency than in the subgroup with normal creatinine levels: 0.057 ± 0.150 μg/l (0.023) vs. 0.022 ± 0.053 μg/l (0.012), respectively ( p < 0.05) (Mann–Whitney test). Conclusion Slightly elevated serum troponin T levels are common in patients with stable coronary artery disease (CAD). We observed a significant correlation between the level of troponin and the presence of atherosclerotic damage to the coronary arteries. A significant correlation between the value of troponin and the extent of atherosclerotic damage (in terms of the number of damaged arteries) could not be demonstrated. On the basis of our findings, the absolute level of troponin T in patients with stable CAD must be interpreted with caution, especially in patients who also have renal insufficiency. Determination of basal troponin T levels in patients with stable CAD is reasonable as they may be used for comparison in case of change in a patient's clinical condition.
ISSN:0010-8650
1803-7712
DOI:10.1016/j.crvasa.2016.12.001