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DOI 10.2174/1389200220666190711114504

Медицинская библиотека · Current drug metabolism · 2019

Serial Quantification of Urinary Protein Biomarkers to Predict Drug-induced Acute Kidney Injury.

Da Yi, Akalya K, Murali Tanusya, Vathsala Anantharaman, Tan Chuen-Seng, Low Sanmay, Lim Hui-Ning, Teo Boon-Wee, Lau Titus, Ong Lizhen, Chua Horng-Ruey

Контролируемое клиническое исследованиеСтатьяПеревод в очереди

Аннотация

BACKGROUND

Drug-induced Acute Kidney Injury (AKI) develops in 10-15% of patients who receive nephrotoxic medications. Urinary biomarkers of renal tubular dysfunction may detect nephrotoxicity early and predict AKI.

METHODS

We prospectively studied patients who received aminoglycosides, vancomycin, amphotericin, or calcineurin inhibitors, and collected their serial urine while on therapy. Patients who developed drug-induced AKI (fulfilling KDIGO criteria) were matched with non-AKI controls in a 1:2 ratio. Their urine samples were batch-analyzed at time-intervals leading up to AKI onset; the latter benchmarked against the final day of nephrotoxic therapy in non- AKI controls. Biomarkers examined include clusterin, beta-2-microglobulin, KIM1, MCP1, cystatin-C, trefoil-factor- 3, NGAL, interleukin-18, GST-Pi, calbindin, and osteopontin; biomarkers were normalized with corresponding urine creatinine.

RESULTS

Nine of 84 (11%) patients developed drug-induced AKI. Biomarkers from 7 AKI cases with pre-AKI samples were compared with those from 14 non-AKI controls. Corresponding mean ages were 55(±17) and 52(±16) years; baseline eGFR were 99(±21) and 101(±24) mL/min/1.73m2 (all p=NS). Most biomarker levels peaked before the onset of AKI. Median levels of 5 biomarkers were significantly higher in AKI cases than controls at 1-3 days before AKI onset (all µg/mmol): clusterin [58(8-411) versus 7(3-17)], beta-2-microglobulin [1632(913-3823) versus 253(61-791)], KIM1 [0.16(0.13-0.76) versus 0.07(0.05-0.15)], MCP1 [0.40(0.16-1.90) versus 0.07(0.04-0.17)], and cystatin-C [33(27-2990) versus 11(7-19)], all p<0.05; their AUROC for AKI prediction were >0.80 (confidence intervals >0.50), with average accuracy highest for clusterin (86%), followed by beta-2-microglobulin, cystatin-C, MCP1, and KIM1 (57%) after cross-validation.

CONCLUSION

Serial surveillance of these biomarkers could improve the lead time for nephrotoxicity detection by days.

Для цитирования: Da Yi, Akalya K, Murali Tanusya, Vathsala Anantharaman, Tan Chuen-Seng, Low Sanmay, Lim Hui-Ning, Teo Boon-Wee, Lau Titus, Ong Lizhen, Chua Horng-Ruey. Serial Quantification of Urinary Protein Biomarkers to Predict Drug-induced Acute Kidney Injury.. Current drug metabolism. 2019. DOI: 10.2174/1389200220666190711114504.

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