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Kinetics of urinary cell cycle arrest markers for acute kidney injury following exposure to potential renal insults

(2018) CRITICAL CARE MEDICINE. 46(3). p.375-383
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Abstract
Objectives: Urinary tissue inhibitor of metalloproteinase-2 and insulin-like growth factor binding protein 7 predict the development of acute kidney injury following renal insults of varied aetiology. To aid clinical interpretation, we describe the kinetics of biomarker elevations around an exposure. Design: In an ancillary analysis of the multicenter SAPPHIRE study, we examined the kinetics of the urinary [tissue inhibitor of metalloproteinase-2]center dot[insulin-like growth factor binding protein 7] in association with exposure to common renal insults (major surgery, IV radiocontrast, vancomycin, nonsteroidal anti-inflammatory drugs, and piperacillin/tazobactam). Setting: Thirty-five sites in North America and Europe between September 2010 and June 2012. Patients: Seven hundred twenty-three critically ill adult patients admitted to the ICU. Interventions: None. Measurements and Main Results: We compared the urinary [tissue metalloproteinase-2]center dot[insulin growth factor binding protein 7] kinetics from the day prior to exposure up to 5 days after exposure in patients developing acute kidney injury stage 2-3, stage 1, or no acute kidney injury by Kidney Disease Improving Global Outcome criteria. Among the 723 patients, 679 (94%) had at least one, 70% had more than one, and 35% had three or more exposures to a known renal insult. There was a significant association between cumulative number of exposures up to study day 3 and risk of acute kidney injury (p = 0.02) but no association between the specific type of exposure and acute kidney injury (p = 0.22). With the exception of radiocontrast, patients who developed acute kidney injury stage 2-3 after one of the five exposures, had a clear rise and fall of urinary [tissue inhibitor of metalloproteinase-2]center dot[insulin-like growth factor binding protein 7] from the day of exposure to 24-48 hours later. In patients without acute kidney injury, there was no significant elevation in urinary [tissue inhibitor of metalloproteinase-2]center dot[insulin-like growth factor binding protein 7]. Conclusions: Exposure to potential renal insults is common. In patients developing acute kidney injury stage 2-3, the kinetics of urinary [tissue inhibitor of metalloproteinase-2]center dot[insulin-like growth factor binding protein 7] matched the exposure except in the case of radiocontrast.
Keywords
acute kidney injury, biomarker, cell-cycle arrest markers, exposures, nephrotoxicity, CRITICALLY-ILL PATIENTS, INTENSIVE-CARE-UNIT, TISSUE INHIBITOR, HIGH-RISK, BIOMARKERS, FAILURE, VALIDATION, PREVENTION, TOXICITY, ENGLAND

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Citation

Please use this url to cite or link to this publication:

MLA
Ostermann, Marlies, Peter A McCullough, Lui G Forni, et al. “Kinetics of Urinary Cell Cycle Arrest Markers for Acute Kidney Injury Following Exposure to Potential Renal Insults.” CRITICAL CARE MEDICINE 46.3 (2018): 375–383. Print.
APA
Ostermann, M., McCullough, P. A., Forni, L. G., Bagshaw, S. M., Joannidis, M., Shi, J., Kashani, K., et al. (2018). Kinetics of urinary cell cycle arrest markers for acute kidney injury following exposure to potential renal insults. CRITICAL CARE MEDICINE, 46(3), 375–383.
Chicago author-date
Ostermann, Marlies, Peter A McCullough, Lui G Forni, Sean M Bagshaw, Michael Joannidis, Jing Shi, Kianoush Kashani, et al. 2018. “Kinetics of Urinary Cell Cycle Arrest Markers for Acute Kidney Injury Following Exposure to Potential Renal Insults.” Critical Care Medicine 46 (3): 375–383.
Chicago author-date (all authors)
Ostermann, Marlies, Peter A McCullough, Lui G Forni, Sean M Bagshaw, Michael Joannidis, Jing Shi, Kianoush Kashani, Patrick M Honore, Lakhmir S Chawla, John A Kellum, on behalf of all SAPPHIRE Investigators, and Eric Hoste. 2018. “Kinetics of Urinary Cell Cycle Arrest Markers for Acute Kidney Injury Following Exposure to Potential Renal Insults.” Critical Care Medicine 46 (3): 375–383.
Vancouver
1.
Ostermann M, McCullough PA, Forni LG, Bagshaw SM, Joannidis M, Shi J, et al. Kinetics of urinary cell cycle arrest markers for acute kidney injury following exposure to potential renal insults. CRITICAL CARE MEDICINE. 2018;46(3):375–83.
IEEE
[1]
M. Ostermann et al., “Kinetics of urinary cell cycle arrest markers for acute kidney injury following exposure to potential renal insults,” CRITICAL CARE MEDICINE, vol. 46, no. 3, pp. 375–383, 2018.
@article{8573773,
  abstract     = {Objectives: Urinary tissue inhibitor of metalloproteinase-2 and insulin-like growth factor binding protein 7 predict the development of acute kidney injury following renal insults of varied aetiology. To aid clinical interpretation, we describe the kinetics of biomarker elevations around an exposure. 
Design: In an ancillary analysis of the multicenter SAPPHIRE study, we examined the kinetics of the urinary [tissue inhibitor of metalloproteinase-2]center dot[insulin-like growth factor binding protein 7] in association with exposure to common renal insults (major surgery, IV radiocontrast, vancomycin, nonsteroidal anti-inflammatory drugs, and piperacillin/tazobactam). 
Setting: Thirty-five sites in North America and Europe between September 2010 and June 2012. 
Patients: Seven hundred twenty-three critically ill adult patients admitted to the ICU. 
Interventions: None. 
Measurements and Main Results: We compared the urinary [tissue metalloproteinase-2]center dot[insulin growth factor binding protein 7] kinetics from the day prior to exposure up to 5 days after exposure in patients developing acute kidney injury stage 2-3, stage 1, or no acute kidney injury by Kidney Disease Improving Global Outcome criteria. Among the 723 patients, 679 (94%) had at least one, 70% had more than one, and 35% had three or more exposures to a known renal insult. There was a significant association between cumulative number of exposures up to study day 3 and risk of acute kidney injury (p = 0.02) but no association between the specific type of exposure and acute kidney injury (p = 0.22). With the exception of radiocontrast, patients who developed acute kidney injury stage 2-3 after one of the five exposures, had a clear rise and fall of urinary [tissue inhibitor of metalloproteinase-2]center dot[insulin-like growth factor binding protein 7] from the day of exposure to 24-48 hours later. In patients without acute kidney injury, there was no significant elevation in urinary [tissue inhibitor of metalloproteinase-2]center dot[insulin-like growth factor binding protein 7]. 
Conclusions: Exposure to potential renal insults is common. In patients developing acute kidney injury stage 2-3, the kinetics of urinary [tissue inhibitor of metalloproteinase-2]center dot[insulin-like growth factor binding protein 7] matched the exposure except in the case of radiocontrast.},
  author       = {Ostermann, Marlies and McCullough, Peter A and Forni, Lui G and Bagshaw, Sean M and Joannidis, Michael and Shi, Jing and Kashani, Kianoush and Honore, Patrick M and Chawla, Lakhmir S and Kellum, John A and SAPPHIRE Investigators, on behalf of all and Hoste, Eric},
  issn         = {0090-3493},
  journal      = {CRITICAL CARE MEDICINE},
  keywords     = {acute kidney injury,biomarker,cell-cycle arrest markers,exposures,nephrotoxicity,CRITICALLY-ILL PATIENTS,INTENSIVE-CARE-UNIT,TISSUE INHIBITOR,HIGH-RISK,BIOMARKERS,FAILURE,VALIDATION,PREVENTION,TOXICITY,ENGLAND},
  language     = {eng},
  number       = {3},
  pages        = {375--383},
  title        = {Kinetics of urinary cell cycle arrest markers for acute kidney injury following exposure to potential renal insults},
  url          = {http://dx.doi.org/10.1097/ccm.0000000000002847},
  volume       = {46},
  year         = {2018},
}

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