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Clin J Am Soc Nephrol. 2012 Jul;7(7):1137-44. doi: 10.2215/CJN.01230212. Epub 2012 May 10.

Subclinical cardiac abnormalities and kidney function decline: the multi-ethnic study of atherosclerosis.

Author information

  • 1Division of Nephrology, Department of Medicine, University of California, San Francisco, CA 94121, USA. meyeon.park@ucsf.edu

Abstract

BACKGROUND AND OBJECTIVES:

Clinical heart failure (HF) is associated with CKD and faster rates of kidney function decline. Whether subclinical abnormalities of cardiac structure are associated with faster kidney function decline is not known. The association between cardiac concentricity and kidney function decline was evaluated.

DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS:

This is a longitudinal study of 3866 individuals from the Multi-Ethnic Study of Atherosclerosis (2000-2007) who were free of clinical cardiovascular disease, with an estimated GFR (eGFR) ≥60 ml/min per 1.73 m(2) at baseline and 5 years of follow-up. Concentricity, a measurement of abnormal cardiac size, was assessed by magnetic resonance imaging and evaluated as a continuous measurement and in quartiles. GFR was estimated by creatinine (eGFRcr) and cystatin C (eGFRcys). The association of concentricity with annual eGFR decline, incident CKD, and rapid kidney function decline (>5% per year) was investigated using linear mixed models as well as Poisson and logistic regression, respectively. Analyses adjusted for demographics, BP, diabetes, and inflammatory markers.

RESULTS:

Median decline was -0.8 (interquartile range, -3.1, -0.5) by eGFRcr. Compared with the lowest quartile of concentricity, persons in the highest quartile had an additional 21% (9%-32%) decline in mean eGFRcr in fully adjusted models. Concentricity was also associated with incident CKD and with rapid kidney function decline after adjustment.

CONCLUSIONS:

Subclinical abnormalities in cardiac structure are associated with longitudinal kidney function decline independent of diabetes and hypertension. Future studies should examine mechanisms to explain these associations.

PMID:
22580783
[PubMed - indexed for MEDLINE]
PMCID:
PMC3386670
Free PMC Article
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