Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury
© 2017 The Author(s). Background: Paraquat ingestion is frequently fatal. While biomarkers of kidney damage increase during paraquat-induced acute kidney injury (AKI), significant concurrent proteinuria may alter diagnostic thresholds for diagnosis and prognosis to an unknown extent. This study eval...
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th-cmuir.6653943832-471912018-04-25T07:25:40Z Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury Fahim Mohamed Nicholas A. Buckley John W. Pickering Klintean Wunnapuk Sandamali Dissanayake Umesh Chathuranga Indika Gawarammana Shaluka Jayamanne Zoltan H. Endre © 2017 The Author(s). Background: Paraquat ingestion is frequently fatal. While biomarkers of kidney damage increase during paraquat-induced acute kidney injury (AKI), significant concurrent proteinuria may alter diagnostic thresholds for diagnosis and prognosis to an unknown extent. This study evaluated the effect of albuminuria on biomarker cutoffs for diagnosis and outcome prediction. Methods: This was a multi-centre prospective clinical study of patients following acute paraquat self-poisoning in 5 Sri Lankan hospitals. Biomarker concentrations were quantified using ELISA and microbead assays and correlated with urinary albumin. Functional-AKI was defined by the Acute Kidney Injury Network serum creatinine definition and alternatively by a ≥50% increase in serum cystatin C. Albuminuria was defined as albumin-creatinine ratio > 30 mg/g. The study outcomes were compared with a retrospective analysis of a pre-clinical study of paraquat-induced nephrotoxicity with appropriate controls. Results: Albuminuria was detected in 34 of 50 patients, and increased with functional-AKI severity. The concentrations of uNGAL, uCysC, uClusterin, uβ2M, and uKIM-1 were higher in albuminuric compared to non-albuminuric patients (p < 0.001). Albuminuria correlated with biomarker concentration (r > 0.6, p < 0.01) and was associated with death (p = 0.006). Optimal biomarker cutoffs for prediction of death were higher in the albuminuric group. Similar outcomes with more detailed analysis were obtained in experimental paraquat nephrotoxicity. Conclusion: Albuminuria was associated with paraquat-induced nephrotoxicity and increased excretion of low-molecular weight protein biomarkers. AKI biomarker cutoffs for diagnosis, outcome prediction and AKI stratification increased in the presence of albuminuria. This may lead to over-diagnosis of AKI in conditions independently associated with proteinuria. 2018-04-25T07:25:40Z 2018-04-25T07:25:40Z 2017-04-03 Journal 14712369 2-s2.0-85016637275 10.1186/s12882-017-0532-7 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85016637275&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/47191 |
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© 2017 The Author(s). Background: Paraquat ingestion is frequently fatal. While biomarkers of kidney damage increase during paraquat-induced acute kidney injury (AKI), significant concurrent proteinuria may alter diagnostic thresholds for diagnosis and prognosis to an unknown extent. This study evaluated the effect of albuminuria on biomarker cutoffs for diagnosis and outcome prediction. Methods: This was a multi-centre prospective clinical study of patients following acute paraquat self-poisoning in 5 Sri Lankan hospitals. Biomarker concentrations were quantified using ELISA and microbead assays and correlated with urinary albumin. Functional-AKI was defined by the Acute Kidney Injury Network serum creatinine definition and alternatively by a ≥50% increase in serum cystatin C. Albuminuria was defined as albumin-creatinine ratio > 30 mg/g. The study outcomes were compared with a retrospective analysis of a pre-clinical study of paraquat-induced nephrotoxicity with appropriate controls. Results: Albuminuria was detected in 34 of 50 patients, and increased with functional-AKI severity. The concentrations of uNGAL, uCysC, uClusterin, uβ2M, and uKIM-1 were higher in albuminuric compared to non-albuminuric patients (p < 0.001). Albuminuria correlated with biomarker concentration (r > 0.6, p < 0.01) and was associated with death (p = 0.006). Optimal biomarker cutoffs for prediction of death were higher in the albuminuric group. Similar outcomes with more detailed analysis were obtained in experimental paraquat nephrotoxicity. Conclusion: Albuminuria was associated with paraquat-induced nephrotoxicity and increased excretion of low-molecular weight protein biomarkers. AKI biomarker cutoffs for diagnosis, outcome prediction and AKI stratification increased in the presence of albuminuria. This may lead to over-diagnosis of AKI in conditions independently associated with proteinuria. |
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Fahim Mohamed Nicholas A. Buckley John W. Pickering Klintean Wunnapuk Sandamali Dissanayake Umesh Chathuranga Indika Gawarammana Shaluka Jayamanne Zoltan H. Endre |
spellingShingle |
Fahim Mohamed Nicholas A. Buckley John W. Pickering Klintean Wunnapuk Sandamali Dissanayake Umesh Chathuranga Indika Gawarammana Shaluka Jayamanne Zoltan H. Endre Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury |
author_facet |
Fahim Mohamed Nicholas A. Buckley John W. Pickering Klintean Wunnapuk Sandamali Dissanayake Umesh Chathuranga Indika Gawarammana Shaluka Jayamanne Zoltan H. Endre |
author_sort |
Fahim Mohamed |
title |
Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury |
title_short |
Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury |
title_full |
Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury |
title_fullStr |
Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury |
title_full_unstemmed |
Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury |
title_sort |
nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury |
publishDate |
2018 |
url |
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85016637275&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/47191 |
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1681423015022166016 |