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Updated: May 17, 2026

A Minimally Invasive Model of Aortic Stenosis in Swine
Published on: October 20, 2023
Copeptin constitutes a novel biomarker of degenerative aortic stenosis
Katarzyna Mizia-Stec1, Bartosz Lasota, Magdalena Mizia
11st Department of Cardiology, Medical University of Silesia, 45/47 Ziołowa, 40-635, Katowice, Poland, kmizia@op.pl.
Insights
Serum copeptin levels are elevated in patients with aortic stenosis (AS), correlating with disease severity. Copeptin shows diagnostic potential for AS, independent of coronary artery disease.
Area of Science:
- Cardiology
- Biomarker Research
- Cardiovascular Diseases
Background:
- Copeptin is an emerging biomarker for cardiovascular diseases.
- The diagnostic utility of copeptin in degenerative aortic stenosis (AS) with preserved left ventricular systolic function remains unclear.
- This study investigates copeptin's role in AS severity and its relationship with coronary artery disease (CAD).
Purpose of the Study:
- To assess serum copeptin levels in patients with degenerative AS and preserved left ventricular systolic function.
- To determine the association between copeptin levels and AS severity (effective orifice area).
- To evaluate if coexisting coronary artery disease (CAD) influences copeptin levels.
Main Methods:
- Sixty-four patients with AS (severe and moderate) and 23 controls were enrolled.
- Serum copeptin and N-terminal pro-brain natriuretic peptide (NT-proBNP) levels were measured using enzyme-linked immunosorbent assay.
- Correlation and receiver-operating characteristic (ROC) analyses were performed.
Main Results:
- Mean serum copeptin concentrations were significantly higher in AS patients (severe: 405 pg/ml, moderate: 351 pg/ml) compared to controls (302 pg/ml).
- Copeptin levels correlated inversely with effective orifice area (EOA) in AS patients (r = -0.55, P < 0.001).
- Copeptin demonstrated good diagnostic performance for severe/moderate AS (sensitivity 71%, specificity 87%) with a cut-off of 354 pg/ml; no correlation with NT-proBNP or CAD was found.
Conclusions:
- Serum copeptin is a novel biomarker for degenerative aortic stenosis.
- Copeptin levels reflect AS severity in patients with preserved left ventricular systolic function.
- Coexisting coronary artery disease does not interfere with copeptin's diagnostic value in AS.
Abstract:
Copeptin is a new biomarker of cardiovascular diseases. Its diagnostic value in degenerative aortic valve stenosis (AS) with preserved left ventricle systolic function is unknown. We aimed to assess the association of serum copeptin levels with AS severity and coexistence of coronary artery disease (CAD). Sixty-four patients with AS and preserved left ventricle systolic function including 40 with severe degenerative AS (group sAS, effective orifice area EOA = 0.67 cm(2)) and 24 with moderate degenerative AS (group mAS, EOA = 1.40 cm(2)) were enrolled into the study. Twenty-three patients without AS and heart failure, matched for age, sex, and CAD occurrence served as the control group (group C). Serum levels of copeptin and N-terminal pro-brain natriuretic peptide (NT-proBNP) were measured using enzyme-linked immunosorbent assay. The mean serum copeptin concentrations were significantly higher in patients with AS: sAS (405 pg/ml) and mAS (351 pg/ml; sAS vs mAS P < 0.05), compared with group C (302 pg/ml, P < 0.05). Serum copeptin levels correlated inversely with EOA (r = -0.55; P < 0.001) in AS patients. There was no correlation between copeptin and NT-proBNP or association with the coexisting CAD. Receiver-operating characteristics analysis showed that copeptin was a good marker of severe/moderate AS (sensitivity 71 %; specificity 87 %), with the optimized cut-off value of 354 pg/ml. Serum copeptin concentration constitutes a novel biomarker of degenerative AS. Coexisting CAD does not interfere with copeptin level.
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