4.6 Article

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

Journal

CLINICAL KIDNEY JOURNAL
Volume 13, Issue 4, Pages 571-579

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ckj/sfz030

Keywords

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

Funding

  1. Fresenius Medical Care, Bad Homburg, Germany
  2. German Ministry of Education and Research [01ER 0804, 01ER 0818, 01ER 0819, 01ER 0820, 01ER 0821]
  3. KfH Foundation for Preventive Medicine

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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. 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. 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(2) [95% CI 1.20-1.37]; former smoking: OR 1.84 [95% CI 1.07-3.17]; lower high-density lipoprotein cholesterol: OR 0.98/mg/dL [95% CI 0.96-1.00] and lower estimated glomerular filtration rate: OR 0.98/mL/min/1.73m(2) [95% CI 0.97-0.99]; all P<0.05} and was not associated with diabetes mellitus, hypertensive nephropathy, total cholesterol and albuminuria. EAT was positively associated with higher ACC-AHA and Framingham risk scores. EAT correlated with coronary artery calcification and aortic valve calcification [Spearman rho = 0.388 (95% CI 0.287-0.532) and r(rb) = 0.409 (95% CI 0.310-0.556), respectively], but these correlations were dependent on CV risk factors. 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.

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