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Ultrasensitive Detection of Biomarkers by Using a Molecular Imprinting Based Capacitive Biosensor
Published on: February 16, 2018
Urinary biomarkers for early detection of platinum based drugs induced nephrotoxicity
Mostafa Abdelsalam1, Ekramy Elmorsy2, Hassan Abdelwahab3
1Mansoura Nephrology and dialysis Unit, Internal Medicine Department, Mansoura Faculty of Medicine, Mansoura University, Mansoura, Egypt. moustafaabdelsalam@yahoo.com.
Background:
Nephrotoxicity is a major hazard complicating the use of platinum based drugs (PBD), which can hinder using higher doses protocols to maximize the therapeutic gain. Shortage of serum creatinine level as an accurate biomarker for acute kidney injuries (AKI) necessitates searching for novel biomarkers with better sensitivity and specificity in patients on PBD.
Methods:
In a prospective cohort design, 132 patients receiving PBD were selected for the study. AKI was diagnosed by continuous follow up of serum creatinine level according to Kidney Disease: Improving Global Outcomes (KDIGO) guidelines 2012. Serum creatinine and urinary biomarkers (KIM-1, NGAL and cystatin C) was measured in the day of treatment and for 3 days after PBD cycle.
Results:
AKI occurred in 35 patients (26.52% of patients). KIM-1, Cystatin C, and NGAL showed significant increase in samples collected in the day of AKI in comparison to their corresponding basal levels (P < 0.0001). In addition, significant increase in urinary levels of the biomarkers in samples collected 1 day before AKI in comparison to their basal levels (P < 0.0001, P < 0.0001, and P = 0.013 for KIM-1, NGAL and Cystatin C respectively). Furthermore KIM-1 data showed a significant increase 2 days before serum creatinine rise in comparison to the corresponding KIM-1 levels in patients who developed AKI (P = 0.001).
Conclusions:
Urinary KIM-1, Cystatin C and NGAL can predict PBD induced AKI in earlier stages than serum createnine. KIM-1 is the most sensitive biomarker for early detection of AKI in patients receiving PBD.
Insights
Urinary biomarkers KIM-1, Cystatin C, and NGAL can detect platinum-based drug nephrotoxicity earlier than serum creatinine. KIM-1 demonstrates the highest sensitivity for early acute kidney injury detection in patients undergoing platinum-based drug therapy.
Area of Science:
- Nephrology
- Oncology
- Biomarker Discovery
Background:
- Platinum-based drugs (PBD) are crucial cancer therapeutics but can cause nephrotoxicity, limiting optimal dosing.
- Serum creatinine is an inadequate biomarker for early detection of acute kidney injury (AKI) in patients receiving PBD.
Purpose of the Study:
- To evaluate novel urinary biomarkers for early detection of PBD-induced AKI.
- To compare the sensitivity of KIM-1, NGAL, and Cystatin C against serum creatinine for AKI prediction.
Main Methods:
- A prospective cohort study included 132 patients receiving PBD.
- AKI diagnosis followed KDIGO guidelines using serum creatinine.
- Urinary biomarkers (KIM-1, NGAL, Cystatin C) and serum creatinine were measured during and after PBD cycles.
Main Results:
- AKI developed in 35 patients (26.52%).
- KIM-1, Cystatin C, and NGAL levels significantly increased on the day of AKI and one day prior.
- KIM-1 showed a significant increase two days before serum creatinine rise in AKI patients.
Conclusions:
- Urinary KIM-1, Cystatin C, and NGAL can predict PBD-induced AKI earlier than serum creatinine.
- KIM-1 is the most sensitive biomarker for the early detection of AKI in patients receiving PBD.
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