Why the study?
Chronic alcohol intake elevates cardiovascular risks, and the diagnostic value of carbohydrate-deficient transferrin compared to traditional biomarkers in heart failure needed evaluation.
Does carbohydrate-deficient transferrin (CDT) correlate with biomarkers of myocardial damage and liver function in patients with advanced heart failure?
Does carbohydrate-deficient transferrin (CDT) correlate with biomarkers of myocardial damage and liver function in patients with advanced heart failure?
In patients with advanced HFrEF, CDT correlates with liver enzymes but not with NT-proBNP or troponin T, serving as a potential marker for undisclosed chronic alcohol consumption.
CDT should not guide myocardial damage assessment in advanced HF; leaves open its role in screening for chronic alcohol use.
Introduction Cardiovascular diseases (CVDs) are the leading cause of death in the world. The dose of 60 g of alcohol / day has been estimated to significantly increase the risk of developing high blood pressure, arrhythmias, hemorrhagic stroke, and cardiomyopathy. The aim of the study was to evaluate the diagnostic value of CDT when compared with gammaglutamyltransferase (GGT), alkaline phosphatase (ALP), N-terminal fragment brain natriuretic peptide (NT pro-BNP) and troponin T biomarkers in patients with heart failure. Materials and Methods The study was conducted on 59 patients with advanced heart failure with reduced ejection fraction (EF<40%). CDT serum levels were measured using CDT kit, Chromsystems Instruments & Chemicals GmbH, Germany and were expressed as a percentage of total transferrin using high-performance liquid chromatography (HPLC). Results Nineteen patients (n = 19) expressed a normal level of carbohydrate deficiency transferrin <1.2% of the total transferrin found in plasma. The results are obtained from 34 patients (n = 34) were within the range doubtful for the test (1.2–2.5%). In 6 Patients (n = 6) the results of more than 2.5% of CDT content were observed, which could indicate chronic alcohol consumption. Conclusions No statistically significant correlations between CDT and troponin T or NT pro-BNP were identified.
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Waś et al. (2023) studied this question.
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