Plasma kidney injury molecule-1 in heart failure: renal mechanisms and clinical outcome

被引:36
作者
Emmens, Johanna E. [1 ]
ter Maaten, Jozine M. [1 ]
Matsue, Yuya [1 ]
Metra, Marco [2 ]
O'Connor, Christopher M. [3 ]
Ponikowski, Piotr [4 ]
Teerlink, John R. [5 ,6 ]
Cotter, Gad [7 ]
Davison, Beth [7 ]
Cleland, John G. [8 ]
Givertz, Michael M. [9 ]
Bloomfield, Daniel M. [10 ]
Dittrich, Howard C. [11 ]
Todd, John [12 ]
van Veldhuisen, Dirk J. [1 ]
Hillege, Hans L. [1 ,13 ]
Damman, Kevin [1 ]
van der Meer, Peter [1 ]
Voors, Adriaan A. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands
[2] Univ Brescia, Brescia, Italy
[3] Duke Univ, Med Ctr, Durham, NC USA
[4] Med Univ, Clin Mil Hosp, Wroclaw, Poland
[5] Univ Calif San Francisco, San Francisco, CA 94143 USA
[6] San Francisco VA Med Ctr, San Francisco, CA USA
[7] Momentum Res, Durham, NC USA
[8] Univ Hull, Kingston Upon Hull, Yorks, England
[9] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[10] Merck Res Labs, Rahway, NJ USA
[11] Univ Iowa, Carver Coll Med, Cardiovasc Res Ctr, Iowa City, IA USA
[12] Singulex Inc, Alameda, CA USA
[13] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
关键词
Plasma KIM-1; Heart failure; Prognosis; TUBULAR DAMAGE; DISEASE; ROLOFYLLINE; ANTAGONIST; MORTALITY; BIOMARKER; KIM-1; RISK;
D O I
10.1002/ejhf.426
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimsUrinary kidney injury molecule-1 (KIM-1) is a marker of tubular damage and associated with worse outcome in heart failure (HF). Plasma KIM-1 has not been described in HF. Methods and resultsIn a renal mechanistic cohort of 120 chronic HF patients, we established the association between plasma KIM-1, renal invasive haemodynamic parameters {renal blood flow ([I-131]hippuran clearance) and measured glomerular filtration rate (GFR; [I-125]iothalamate)} and urinary tubular damage markers. The association between plasma KIM-1, plasma creatinine, and clinical outcome was further explored in a cohort of 2033 acute HF patients. Median plasma KIM-1 was 171.5pg/mL (122.8-325.7) in chronic (n = 99) and 295.1pg/mL (182.2-484.2) in acute HF (n = 1588). In chronic HF, plasma KIM-1 was associated with GFR (P < 0.001), creatinine, and cystatin C. Plasma KIM-1 was associated with urinary N-acetyl--d-glucosaminidase (NAG), but not with other urinary tubular damage markers. Log plasma KIM-1 predicted adverse clinical outcome after adjustment for age, gender, and GFR [hazard ratio (HR) 1.94, 95% confidence interval (CI) 1.07-3.53, P = 0.030]. Statistical significance was lost after correction for NT-proBNP (HR 1.61, 95% CI 0.81-3.20, P = 0.175). In acute HF, higher plasma KIM-1 levels were associated with higher creatinine, lower albumin, and presence of diabetes. Log plasma KIM-1 predicted 60-day HF rehospitalization (HR 1.27, 95% CI 1.03-1.55, P = 0.024), but not 180-day mortality or 60-day death or renal or cardiovascular rehospitalization. ConclusionsPlasma KIM-1 is associated with glomerular filtration and urinary NAG, but not with other urinary tubular damage markers. Plasma KIM-1 does not predict outcome in chronic HF after correction for NT-proBNP. In acute HF, plasma KIM-1 predicts HF rehospitalization in multivariable analysis.
引用
收藏
页码:641 / 649
页数:9
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