Derivation and validation of cutoffs for clinical use of cell cycle arrest biomarkers

被引:209
作者
Hoste, Eric A. J. [1 ]
McCullough, Peter A. [2 ,3 ]
Kashani, Kianoush [4 ]
Chawla, Lakhmir S. [5 ,6 ,7 ]
Joannidis, Michael [8 ]
Shaw, Andrew D. [9 ]
Feldkamp, Thorsten [10 ,11 ]
Uettwiller-Geiger, Denise L. [12 ]
McCarthy, Paul [13 ]
Shi, Jing [14 ]
Walker, Michael G. [14 ]
Kellum, John A. [15 ]
机构
[1] Univ Ghent, Ghent Univ Hosp, Intens Care Unit, B-9000 Ghent, Belgium
[2] Baylor Univ, Baylor Jack & Jane Hamilton Heart & Vasc Hosp, Baylor Heart & Vasc Inst, Med Ctr, Dallas, TX USA
[3] Heart Hosp, Plano, TX USA
[4] Mayo Clin, Div Pulm & Crit Care Med, Rochester, MN USA
[5] Vet Affairs Med Ctr, Dept Med, Div Intens Care Med, Washington, DC 20422 USA
[6] Vet Affairs Med Ctr, Div Nephrol, Washington, DC 20422 USA
[7] George Washington Univ, Dept Anesthesiol & Crit Care Med, Washington, DC USA
[8] Med Univ Innsbruck, ICU, Dept Internal Med, A-6020 Innsbruck, Austria
[9] Vanderbilt Univ, Med Ctr, Dept Anesthesia, Nashville, TN USA
[10] Univ Duisburg Essen, Univ Hosp Essen, Dept Nephrol, Essen, Germany
[11] Univ Kiel, Univ Hosp Schleswig Holstein, Dept Hypertens & Nephrol, Kiel, Germany
[12] JT Mather Mem Hosp, Clin Lab Trials, Port Jefferson, NY USA
[13] Univ Maryland, Med Ctr, R Adams Cowley Shock Trauma Ctr, Baltimore, MD 21201 USA
[14] Walker Biosci, Carlsbad, CA USA
[15] Univ Pittsburgh, Sch Med, Dept Crit Care Med, Ctr Crit Care Nephrol, Pittsburgh, PA 15260 USA
关键词
acute kidney injury; acute renal failure; biomarkers; insulin-like growth factor binding protein (IGFBP)7 and tissue inhibitor of metalloproteinases (TIMP)-2; sensitivity and specificity (MeSH); ACUTE KIDNEY INJURY; RENAL-FUNCTION; MORTALITY; PROGNOSIS; DIAGNOSIS; TRIAL;
D O I
10.1093/ndt/gfu292
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Acute kidney injury (AKI) remains a deadly condition. Tissue inhibitor of metalloproteinases (TIMP)-2 and insulin-like growth factor binding protein (IGFBP)7 are two recently discovered urinary biomarkers for AKI. We now report on the development, and diagnostic accuracy of two clinical cutoffs for a test using these markers. We derived cutoffs based on sensitivity and specificity for prediction of Kidney Disease: Improving Global Outcomes Stages 2-3 AKI within 12 h using data from a previously published multicenter cohort (Sapphire). Next, we verified these cutoffs in a new study (Opal) enrolling 154 critically ill adults from six sites in the USA. One hundred subjects (14%) in Sapphire and 27 (18%) in Opal met the primary end point. The results of the Opal study replicated those of Sapphire. Relative risk (95% CI) in both studies for subjects testing at a parts per thousand currency sign0.3 versus > 0.3-2 were 4.7 (1.5-16) and 4.4 (2.5-8.7), or 12 (4.2-40) and 18 (10-37) for a parts per thousand currency sign0.3 versus > 2. For the 0.3 cutoff, sensitivity was 89% in both studies, and specificity 50 and 53%. For 2.0, sensitivity was 42 and 44%, and specificity 95 and 90%. Urinary [TIMP-2]aEuro cent[IGFBP7] values of 0.3 or greater identify patients at high risk and those > 2 at highest risk for AKI and provide new information to support clinical decision-making. Clintrials.gov # NCT01209169 (Sapphire) and NCT01846884 (Opal).
引用
收藏
页码:2054 / 2061
页数:8
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