Epicardial fat, cardiovascular risk factors and calcifications in patients with chronic kidney disease.

Framingham risk score atherosclerotic cardiovascular disease risk score chronic kidney disease epicardial adipose tissue vascular calcification

Journal

Clinical kidney journal
ISSN: 2048-8505
Titre abrégé: Clin Kidney J
Pays: England
ID NLM: 101579321

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 26 09 2018
accepted: 19 02 2019
entrez: 9 9 2020
pubmed: 8 4 2019
medline: 8 4 2019
Statut: epublish

Résumé

Epicardial adipose tissue (EAT) exerts cardiopathogenic effects, but the independent association between EAT and cardiovascular (CV) calcification in patients with chronic kidney disease (CKD) remains controversial. We therefore assessed the association between EAT, CV risk factors and CV calcifications. 257 patients with CKD Stage 3 and/or overt proteinuria underwent quantification of EAT, coronary artery calcification and aortic valve calcification by computed tomography. Framingham and American College of Cardiology and American Heart Association (ACC-AHA) 10-year CV event risk scores were calculated for each patient. Using multivariable regression analysis, higher EAT was significantly associated with the majority of investigated risk factors {higher age: odds ratio [OR] 1.05/year [95% confidence interval (CI) 1.02-1.08]; male sex: OR 4.03 [95% CI 2.22-7.31]; higher BMI: OR 1.28/kg/m The increase of EAT can be explained by individual CV risk factors and kidney function and correlates with 10-year risk for CV event scores, suggesting that EAT is a modifiable risk factor in patients with CKD. Although EAT correlates with CV calcifications, these relations depend on CV risk factors.

Sections du résumé

BACKGROUND BACKGROUND
Epicardial adipose tissue (EAT) exerts cardiopathogenic effects, but the independent association between EAT and cardiovascular (CV) calcification in patients with chronic kidney disease (CKD) remains controversial. We therefore assessed the association between EAT, CV risk factors and CV calcifications.
METHODS METHODS
257 patients with CKD Stage 3 and/or overt proteinuria underwent quantification of EAT, coronary artery calcification and aortic valve calcification by computed tomography. Framingham and American College of Cardiology and American Heart Association (ACC-AHA) 10-year CV event risk scores were calculated for each patient.
RESULTS RESULTS
Using multivariable regression analysis, higher EAT was significantly associated with the majority of investigated risk factors {higher age: odds ratio [OR] 1.05/year [95% confidence interval (CI) 1.02-1.08]; male sex: OR 4.03 [95% CI 2.22-7.31]; higher BMI: OR 1.28/kg/m
CONCLUSIONS CONCLUSIONS
The increase of EAT can be explained by individual CV risk factors and kidney function and correlates with 10-year risk for CV event scores, suggesting that EAT is a modifiable risk factor in patients with CKD. Although EAT correlates with CV calcifications, these relations depend on CV risk factors.

Identifiants

pubmed: 32905245
doi: 10.1093/ckj/sfz030
pii: sfz030
pmc: PMC7467583
doi:

Types de publication

Journal Article

Langues

eng

Pagination

571-579

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of ERA-EDTA.

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Auteurs

Turgay Saritas (T)

Department of Nephrology and Clinical Immunology, University Hospital RWTH Aachen, Aachen, Germany.

Sebastian Daniel Reinartz (SD)

Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Aachen, Germany.

Jennifer Nadal (J)

Department of Medical Biometry, Informatics, and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany.

Jonas Schmoee (J)

Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Aachen, Germany.

Matthias Schmid (M)

Department of Medical Biometry, Informatics, and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany.

Mohamed Marwan (M)

Department of Cardiology, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.

Stephan Achenbach (S)

Department of Cardiology, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.

Stefan Störk (S)

Division of Cardiology (Comprehensive Heart Failure Center), Department of Medicine I, University Hospital Würzburg, Würzburg, Germany.

Christoph Wanner (C)

Division of Nephrology, Department of Medicine, University Hospital Würzburg, Würzburg, Germany.

Kai-Uwe Eckardt (KU)

Department of Nephrology and Medical Intensive Care, Charité Universitätsmedizin Berlin, Berlin, Germany.
Department of Nephrology and Hypertension, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.

Jürgen Floege (J)

Department of Nephrology and Clinical Immunology, University Hospital RWTH Aachen, Aachen, Germany.

Markus Peter Schneider (M)

Department of Nephrology and Hypertension, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Department of Nephrology and Hypertension, Klinikum Nürnberg, Paracelsus Private Medical University, Nürnberg, Germany.

Georg Schlieper (G)

Department of Nephrology and Clinical Immunology, University Hospital RWTH Aachen, Aachen, Germany.

Classifications MeSH