Association of Urinary Injury Biomarkers with Mortality and Cardiovascular Events

Kidney damage is a common sequela of several chronic pathologic conditions. Whether biomarkers of kidney damage are prognostic for more severe outcomes is unknown. We measured three urinary biomarkers (kidney injury molecule-1 [KIM-1], IL-18, and albumin) in 3010 individuals enrolled in the Health,...

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Veröffentlicht in:Journal of the American Society of Nephrology 2014-07, Vol.25 (7), p.1545-1553
Hauptverfasser: SARNAK, Mark J, KATZ, Ronit, SIMONSICK, Eleanor M, PARIKH, Chirag R, SHLIPAK, Michael G, NEWMAN, Anne, HARRIS, Tamara, PERALTA, Carmen A, DEVARAJAN, Prasad, BENNETT, Michael R, FRIED, Linda, IX, Joachim H, SATTERFIELD, Suzanne
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container_end_page 1553
container_issue 7
container_start_page 1545
container_title Journal of the American Society of Nephrology
container_volume 25
creator SARNAK, Mark J
KATZ, Ronit
SIMONSICK, Eleanor M
PARIKH, Chirag R
SHLIPAK, Michael G
NEWMAN, Anne
HARRIS, Tamara
PERALTA, Carmen A
DEVARAJAN, Prasad
BENNETT, Michael R
FRIED, Linda
IX, Joachim H
SATTERFIELD, Suzanne
description Kidney damage is a common sequela of several chronic pathologic conditions. Whether biomarkers of kidney damage are prognostic for more severe outcomes is unknown. We measured three urinary biomarkers (kidney injury molecule-1 [KIM-1], IL-18, and albumin) in 3010 individuals enrolled in the Health, Aging and Body Composition (Health ABC) study and used Cox proportional hazards models to investigate the associations of urinary KIM-1/creatinine (cr), IL-18/cr, and albumin/cr (ACR) with all-cause mortality and cardiovascular disease (CVD). Multivariable models adjusted for demographics, traditional CVD risk factors, and eGFR. Mean age of participants was 74 years, 49% of participants were men, and 41% of participants were black. During the median 12.4 years of follow-up, 1450 deaths and 797 CVD outcomes occurred. Compared with the lowest quartile, successive quartiles had the following adjusted hazard ratios (HRs; 95% confidence intervals [95% CIs]) for mortality: KIM-1/cr: (1.21; 1.03 to 1.41), (1.13; 0.96 to 1.34), and (1.28; 1.08 to 1.52); IL-18/cr: (1.02; 0.88 to 1.19), (1.16; 0.99 to 1.35), and (1.06; 0.90 to 1.25); ACR: (1.08; 0.91 to 1.27), (1.24; 1.06 to 1.46), and (1.63; 1.39 to 1.91). In similar analyses, only ACR quartiles associated with CVD: (1.19; 0.95 to 1.48), (1.35; 1.08 to 1.67), and (1.54; 1.24 to 1.91). Urinary KIM-1 had a modest association with all-cause mortality but did not associate with CVD, and urinary IL-18 did not associate with either outcome. In contrast, albuminuria strongly associated with all-cause mortality and CVD. Future studies should evaluate reasons for these differences in the prognostic importance of individual kidney injury markers.
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Whether biomarkers of kidney damage are prognostic for more severe outcomes is unknown. We measured three urinary biomarkers (kidney injury molecule-1 [KIM-1], IL-18, and albumin) in 3010 individuals enrolled in the Health, Aging and Body Composition (Health ABC) study and used Cox proportional hazards models to investigate the associations of urinary KIM-1/creatinine (cr), IL-18/cr, and albumin/cr (ACR) with all-cause mortality and cardiovascular disease (CVD). Multivariable models adjusted for demographics, traditional CVD risk factors, and eGFR. Mean age of participants was 74 years, 49% of participants were men, and 41% of participants were black. During the median 12.4 years of follow-up, 1450 deaths and 797 CVD outcomes occurred. Compared with the lowest quartile, successive quartiles had the following adjusted hazard ratios (HRs; 95% confidence intervals [95% CIs]) for mortality: KIM-1/cr: (1.21; 1.03 to 1.41), (1.13; 0.96 to 1.34), and (1.28; 1.08 to 1.52); IL-18/cr: (1.02; 0.88 to 1.19), (1.16; 0.99 to 1.35), and (1.06; 0.90 to 1.25); ACR: (1.08; 0.91 to 1.27), (1.24; 1.06 to 1.46), and (1.63; 1.39 to 1.91). In similar analyses, only ACR quartiles associated with CVD: (1.19; 0.95 to 1.48), (1.35; 1.08 to 1.67), and (1.54; 1.24 to 1.91). Urinary KIM-1 had a modest association with all-cause mortality but did not associate with CVD, and urinary IL-18 did not associate with either outcome. In contrast, albuminuria strongly associated with all-cause mortality and CVD. 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Future studies should evaluate reasons for these differences in the prognostic importance of individual kidney injury markers.</abstract><cop>Washington, DC</cop><pub>American Society of Nephrology</pub><pmid>24511130</pmid><doi>10.1681/ASN.2013070713</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Albuminuria - urine
Biological and medical sciences
Biomarkers - urine
Cardiovascular Diseases - mortality
Cardiovascular Diseases - urine
Cause of Death
Clinical Epidemiology
Female
Hepatitis A Virus Cellular Receptor 1
Humans
Interleukin-18 - urine
Male
Medical sciences
Membrane Glycoproteins - urine
Nephrology. Urinary tract diseases
Receptors, Virus
title Association of Urinary Injury Biomarkers with Mortality and Cardiovascular Events
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