Association of MR-proadrenomedullin with cardiovascular risk factors and subclinical cardiovascular disease

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Association of MR-proadrenomedullin with cardiovascular risk factors and subclinical cardiovascular disease. / Neumann, Johannes Tobias; Tzikas, Stergios; Funke-Kaiser, Anne; Wilde, Sandra; Appelbaum, Sebastian; Keller, Till; Ojeda-Echevarria, Francisco; Zeller, Tanja; Zwiener, Isabella; Sinning, Christoph R; Jagodzinski, Annika; Schnabel, Renate B; Lackner, Karl J; Münzel, Thomas; Blankenberg, Stefan; Wild, Philipp S; Sydow, Karsten.

In: ATHEROSCLEROSIS, Vol. 228, No. 2, 06.2013, p. 451-459.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Neumann, JT, Tzikas, S, Funke-Kaiser, A, Wilde, S, Appelbaum, S, Keller, T, Ojeda-Echevarria, F, Zeller, T, Zwiener, I, Sinning, CR, Jagodzinski, A, Schnabel, RB, Lackner, KJ, Münzel, T, Blankenberg, S, Wild, PS & Sydow, K 2013, 'Association of MR-proadrenomedullin with cardiovascular risk factors and subclinical cardiovascular disease', ATHEROSCLEROSIS, vol. 228, no. 2, pp. 451-459. https://doi.org/10.1016/j.atherosclerosis.2013.03.006

APA

Neumann, J. T., Tzikas, S., Funke-Kaiser, A., Wilde, S., Appelbaum, S., Keller, T., Ojeda-Echevarria, F., Zeller, T., Zwiener, I., Sinning, C. R., Jagodzinski, A., Schnabel, R. B., Lackner, K. J., Münzel, T., Blankenberg, S., Wild, P. S., & Sydow, K. (2013). Association of MR-proadrenomedullin with cardiovascular risk factors and subclinical cardiovascular disease. ATHEROSCLEROSIS, 228(2), 451-459. https://doi.org/10.1016/j.atherosclerosis.2013.03.006

Vancouver

Bibtex

@article{b895fc8b8ffd402dae8507cde1485ebc,
title = "Association of MR-proadrenomedullin with cardiovascular risk factors and subclinical cardiovascular disease",
abstract = "AIMS AND BACKGROUND: Midregional proadrenomedullin (MR-proADM) is a protein, which exerts various effects on the cardiovascular system. Recent studies underscored its prognostic implications in patients with acute dyspnea and cardiovascular diseases. Therefore, we aimed to determine the distribution of MR-proADM in the general population and to reveal potential associations of MR-proADM with cardiovascular risk factors and measures of subclinical cardiovascular disease.METHODS AND RESULTS: MR-proADM plasma concentrations were determined in individuals of the population-based cohort of the Gutenberg Health Study (N = 5000) using a commercially available fluoroimmunoassay. Individuals were enrolled between April 2007 and October 2008. Subclinical cardiovascular disease was assessed using echocardiographic and functional measures of myocardial and vascular function. The mean age of the study population was 55.5 ± 10.9 years. In the overall population we determined a median MR-proADM plasma concentration of 0.44 nmol/L in men and women. MR-proADM concentrations were elevated in individuals with hypertension, diabetes, dyslipidemia, known cardiovascular disease, heart failure, peripheral artery disease, atrial fibrillation, and history of myocardial infarction and stroke. In men, we observed a positive association of MR-proADM with reduced ejection fraction, intraventricular septal diameter, wall thickness, and echocardiographic measures of diastolic dysfunction.CONCLUSIONS: In this study, we present age-dependent reference values for MR-proADM in a representative population sample. Elevated MR-proADM plasma concentrations were strongly associated with classical cardiovascular risk factors and manifest cardiovascular diseases. Furthermore, we revealed a gender-specific association with echocardiographic measures of hypertension. MR-proADM seems to be a promising prognostic biomarker for subclinical and manifest cardiovascular disease.",
keywords = "Adrenomedullin/blood, Adult, Age Factors, Aged, Asymptomatic Diseases, Biomarkers/blood, Cardiovascular Diseases/blood, Cross-Sectional Studies, Echocardiography, Female, Fluoroimmunoassay, Germany/epidemiology, Humans, Linear Models, Male, Middle Aged, Peptide Fragments/blood, Phenotype, Predictive Value of Tests, Prevalence, Prognosis, Prospective Studies, Protein Precursors/blood, Risk Assessment, Risk Factors, Sex Factors, Up-Regulation",
author = "Neumann, {Johannes Tobias} and Stergios Tzikas and Anne Funke-Kaiser and Sandra Wilde and Sebastian Appelbaum and Till Keller and Francisco Ojeda-Echevarria and Tanja Zeller and Isabella Zwiener and Sinning, {Christoph R} and Annika Jagodzinski and Schnabel, {Renate B} and Lackner, {Karl J} and Thomas M{\"u}nzel and Stefan Blankenberg and Wild, {Philipp S} and Karsten Sydow",
note = "Copyright {\textcopyright} 2013 Elsevier Ireland Ltd. All rights reserved.",
year = "2013",
month = jun,
doi = "10.1016/j.atherosclerosis.2013.03.006",
language = "English",
volume = "228",
pages = "451--459",
journal = "ATHEROSCLEROSIS",
issn = "0021-9150",
publisher = "Elsevier Ireland Ltd",
number = "2",

}

RIS

TY - JOUR

T1 - Association of MR-proadrenomedullin with cardiovascular risk factors and subclinical cardiovascular disease

AU - Neumann, Johannes Tobias

AU - Tzikas, Stergios

AU - Funke-Kaiser, Anne

AU - Wilde, Sandra

AU - Appelbaum, Sebastian

AU - Keller, Till

AU - Ojeda-Echevarria, Francisco

AU - Zeller, Tanja

AU - Zwiener, Isabella

AU - Sinning, Christoph R

AU - Jagodzinski, Annika

AU - Schnabel, Renate B

AU - Lackner, Karl J

AU - Münzel, Thomas

AU - Blankenberg, Stefan

AU - Wild, Philipp S

AU - Sydow, Karsten

N1 - Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

PY - 2013/6

Y1 - 2013/6

N2 - AIMS AND BACKGROUND: Midregional proadrenomedullin (MR-proADM) is a protein, which exerts various effects on the cardiovascular system. Recent studies underscored its prognostic implications in patients with acute dyspnea and cardiovascular diseases. Therefore, we aimed to determine the distribution of MR-proADM in the general population and to reveal potential associations of MR-proADM with cardiovascular risk factors and measures of subclinical cardiovascular disease.METHODS AND RESULTS: MR-proADM plasma concentrations were determined in individuals of the population-based cohort of the Gutenberg Health Study (N = 5000) using a commercially available fluoroimmunoassay. Individuals were enrolled between April 2007 and October 2008. Subclinical cardiovascular disease was assessed using echocardiographic and functional measures of myocardial and vascular function. The mean age of the study population was 55.5 ± 10.9 years. In the overall population we determined a median MR-proADM plasma concentration of 0.44 nmol/L in men and women. MR-proADM concentrations were elevated in individuals with hypertension, diabetes, dyslipidemia, known cardiovascular disease, heart failure, peripheral artery disease, atrial fibrillation, and history of myocardial infarction and stroke. In men, we observed a positive association of MR-proADM with reduced ejection fraction, intraventricular septal diameter, wall thickness, and echocardiographic measures of diastolic dysfunction.CONCLUSIONS: In this study, we present age-dependent reference values for MR-proADM in a representative population sample. Elevated MR-proADM plasma concentrations were strongly associated with classical cardiovascular risk factors and manifest cardiovascular diseases. Furthermore, we revealed a gender-specific association with echocardiographic measures of hypertension. MR-proADM seems to be a promising prognostic biomarker for subclinical and manifest cardiovascular disease.

AB - AIMS AND BACKGROUND: Midregional proadrenomedullin (MR-proADM) is a protein, which exerts various effects on the cardiovascular system. Recent studies underscored its prognostic implications in patients with acute dyspnea and cardiovascular diseases. Therefore, we aimed to determine the distribution of MR-proADM in the general population and to reveal potential associations of MR-proADM with cardiovascular risk factors and measures of subclinical cardiovascular disease.METHODS AND RESULTS: MR-proADM plasma concentrations were determined in individuals of the population-based cohort of the Gutenberg Health Study (N = 5000) using a commercially available fluoroimmunoassay. Individuals were enrolled between April 2007 and October 2008. Subclinical cardiovascular disease was assessed using echocardiographic and functional measures of myocardial and vascular function. The mean age of the study population was 55.5 ± 10.9 years. In the overall population we determined a median MR-proADM plasma concentration of 0.44 nmol/L in men and women. MR-proADM concentrations were elevated in individuals with hypertension, diabetes, dyslipidemia, known cardiovascular disease, heart failure, peripheral artery disease, atrial fibrillation, and history of myocardial infarction and stroke. In men, we observed a positive association of MR-proADM with reduced ejection fraction, intraventricular septal diameter, wall thickness, and echocardiographic measures of diastolic dysfunction.CONCLUSIONS: In this study, we present age-dependent reference values for MR-proADM in a representative population sample. Elevated MR-proADM plasma concentrations were strongly associated with classical cardiovascular risk factors and manifest cardiovascular diseases. Furthermore, we revealed a gender-specific association with echocardiographic measures of hypertension. MR-proADM seems to be a promising prognostic biomarker for subclinical and manifest cardiovascular disease.

KW - Adrenomedullin/blood

KW - Adult

KW - Age Factors

KW - Aged

KW - Asymptomatic Diseases

KW - Biomarkers/blood

KW - Cardiovascular Diseases/blood

KW - Cross-Sectional Studies

KW - Echocardiography

KW - Female

KW - Fluoroimmunoassay

KW - Germany/epidemiology

KW - Humans

KW - Linear Models

KW - Male

KW - Middle Aged

KW - Peptide Fragments/blood

KW - Phenotype

KW - Predictive Value of Tests

KW - Prevalence

KW - Prognosis

KW - Prospective Studies

KW - Protein Precursors/blood

KW - Risk Assessment

KW - Risk Factors

KW - Sex Factors

KW - Up-Regulation

U2 - 10.1016/j.atherosclerosis.2013.03.006

DO - 10.1016/j.atherosclerosis.2013.03.006

M3 - SCORING: Journal article

C2 - 23562132

VL - 228

SP - 451

EP - 459

JO - ATHEROSCLEROSIS

JF - ATHEROSCLEROSIS

SN - 0021-9150

IS - 2

ER -