Urinary kidney injury molecule 1 (KIM-1) and interleukin 18 (IL-18) as risk markers for heart failure in older adults: the Health, Aging, and Body Composition (Health ABC) Study.
Urinary kidney injury molecule 1 (KIM-1) and interleukin 18 (IL-18) as risk markers for heart failure in older adults: the Health, Aging, and Body Composition (Health ABC) Study.
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DOI:
10.1053/j.ajkd.2014.01.432
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发表时间:
2014-07
期刊:
影响因子:
--
通讯作者:
Health ABC Study
中科院分区:
文献类型:
--
作者:
Driver TH;Katz R;Ix JH;Magnani JW;Peralta CA;Parikh CR;Fried L;Newman AB;Kritchevsky SB;Sarnak MJ;Shlipak MG;Health ABC Study
Kidney damage and reduced kidney function are potent risk factors for heart failure (HF), but existing studies are limited to assessing albuminuria or estimated glomerular filtration rate (eGFR). We evaluated the associations of urinary biomarkers of kidney tubular injury (interleukin 18 [IL-18] and kidney injury molecule 1 [KIM-1]) with future risk of HF. Retrospective cohort study. 2921 participants without HF in the Health, Aging, and Body Composition (Health ABC) cohort. Ratios of urine KIM-1, IL-18, and albumin to creatinine (KIM-1:Cr, IL-18:Cr, and ACR, respectively). Incident HF over a median follow-up of 12 years. Median values of each marker at baseline were 812 (IQR, 497–1235) pg/mg for KIM-1:Cr, 31 (IQR, 19–56) pg/mg for IL-18:Cr, and 8 (IQR, 5–19) mg/g for ACR. 596 persons developed HF during follow-up. The top quartile of KIM-1:Cr was associated with risk of incident HF after adjustment for baseline eGFR, HF risk factors, and ACR (HR, 1.32; 95% CI, 1.02–1.70) in adjusted multivariate proportional hazards models. The top quartile of IL-18:Cr was also associated with HF in a model adjusted for risk factors and eGFR (HR, 1.35; 95% CI, 1.05–1.73), but was attenuated by adjustment for ACR (HR, 1.15; 95% CI, 0.89–1.48). The top quartile of ACR had a stronger adjusted association with HF (HR, 1.96; 95% CI, 1.53–2.51). Generalizability to other populations is uncertain. Higher urine concentrations of KIM-1 were independently associated with incident HF risk, although the associations of higher ACR were of stronger magnitude.
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DOI:
10.1056/nejmoa1114248
发表时间:
2012-07-05
期刊:
The New England journal of medicine
影响因子:
--
作者:
Inker LA;Schmid CH;Tighiouart H;Eckfeldt JH;Feldman HI;Greene T;Kusek JW;Manzi J;Van Lente F;Zhang YL;Coresh J;Levey AS;CKD-EPI Investigators
通讯作者:
CKD-EPI Investigators
DOI:
10.1053/j.ajkd.2011.02.391
发表时间:
2011-07
期刊:
American journal of kidney diseases : the official journal of the National Kidney Foundation
影响因子:
--
作者:
Blecker S;Matsushita K;Köttgen A;Loehr LR;Bertoni AG;Boulware LE;Coresh J
通讯作者:
Coresh J
影响因子:
13.6
作者:
Parikh, CR;Abraham, E;Edelstein, CL
通讯作者:
Edelstein, CL
影响因子:
13.6
作者:
Koyner, Jay L.;Garg, Amit X.;Parikh, Chirag R.
通讯作者:
Parikh, Chirag R.
DOI:
10.1053/j.ajkd.2012.05.014
发表时间:
2012-12
期刊:
American journal of kidney diseases : the official journal of the National Kidney Foundation
影响因子:
--
作者:
Peralta CA;Katz R;Bonventre JV;Sabbisetti V;Siscovick D;Sarnak M;Shlipak MG
通讯作者:
Shlipak MG