Urinary cell cycle arrest biomarkers and chitinase 3-like protein 1 (CHI3L1) to detect acute kidney injury in the critically ill: a post hoc laboratory analysis on the FINNAKI cohort
Autor: | Hoste, Eric, The FINNAKI Study Group, [missing], Vaara, Suvi T., De Loor, Jorien, Haapio, Mikko, Nuytinck, Lieve, Demeyere, Kristel, Pettilä, Ville, Meyer, Evelyne |
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Přispěvatelé: | HUS Perioperative, Intensive Care and Pain Medicine, Anestesiologian yksikkö, University of Helsinki, Helsinki University Hospital Area, HUS Abdominal Center, Nefrologian yksikkö, Department of Medicine, Department of Diagnostics and Therapeutics |
Rok vydání: | 2020 |
Předmět: |
Male
Letter 030204 cardiovascular system & hematology Kidney urologic and male genital diseases GUIDELINES Critical Care and Intensive Care Medicine Likelihood ratios in diagnostic testing 0302 clinical medicine Medicine and Health Sciences Clinical endpoint EPIDEMIOLOGY FAILURE Prospective Studies Biological markers lcsh:Medical emergencies. Critical care. Intensive care. First aid Acute kidney injury Area under the curve Middle Aged female genital diseases and pregnancy complications Lipocalins 3. Good health Cohort Biomarker (medicine) Female medicine.medical_specialty YKL-40 Critical Illness Urinary system 03 medical and health sciences INFLAMMATION Internal medicine Intensive care medicine Humans Chitinase-3-Like Protein 1 Aged SEPSIS business.industry Chitinase NephroCheck 030208 emergency & critical care medicine Cell Cycle Checkpoints lcsh:RC86-88.9 3126 Surgery anesthesiology intensive care radiology medicine.disease MARKER business Biomarkers |
Zdroj: | CRITICAL CARE Critical Care, Vol 24, Iss 1, Pp 1-10 (2020) Critical Care |
ISSN: | 1364-8535 1466-609X |
Popis: | Background Acute kidney injury (AKI) is a frequently occurring syndrome in critically ill patients and is associated with worse outcomes. Biomarkers allow early identification and therapy of AKI which may improve outcomes. Urine chitinase 3-like protein 1 (uCHI3L1) was recently identified as a promising urinary biomarker for AKI. In this multicenter study, we evaluated the diagnostic performance for AKI stage 2 or greater of uCHI3L1 in comparison with the urinary cell cycle arrest biomarkers urinary tissue inhibitor of metalloproteinases-2 (TIMP-2)•insulin-like growth factor-binding protein 7 (IGFBP7) measured by NephroCheck Risk®. Methods Post hoc laboratory study of the prospective observational FINNAKI study. Of this cohort, we included patients with stored admission urine samples and availability of serum creatinine at day 1 of admission. Patients who already had AKI stage 2 or 3 at ICU admission were excluded. AKI was defined and staged according to the KDIGO definition and staging system. The primary endpoint was AKI stage 2 or 3 at day 1. Biomarker performance was assessed by the area under the curve of the receiver operating characteristic curve (AUC). We assessed individual performance and different combinations of urine biomarkers. Results Of 660 included patients, 49 (7.4%) had AKI stages 2–3 at day 1. All urine biomarkers were increased at admission in AKI patients. All biomarkers and most combinations had AUCs Conclusions We found that uCHI3L1 and NephroCheck Risk® had a comparable diagnostic performance for diagnosis of AKI stage 2 or greater within a 24-h period in this multicenter FINNAKI cohort. In contrast to initial discovery and validation studies, the diagnostic performance was poor. Possible explanations for this observation are differences in patient populations, proportion of emergency admissions, proportion of functional AKI, rate of developing AKI, and observation periods for diagnosis of AKI. |
Databáze: | OpenAIRE |
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