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Qualified kidney biomarkers and their potential significance in drug safety evaluation and prediction. | LitMetric

AI Article Synopsis

  • The kidney is a key organ affected by drug toxicity, and traditional biomarkers like serum creatinine and blood urea nitrogen are often insufficient for accurately assessing kidney injury.
  • There is a pressing need for new kidney safety biomarkers to detect and predict drug-induced nephrotoxicity during various stages of drug development and patient care.
  • Eight new renal safety biomarkers have been identified, with some focusing on proximal tubular injury and others on glomerular damage, allowing for a comprehensive approach to evaluating kidney safety in drug research and clinical applications.

Article Abstract

The kidney is one of the major organs drug toxicity may target. Some renal safety biomarkers have been proposed to measure kidney injury and function accordingly. Despite the widespread use for diagnosis and monitoring of renal injury and function for decades, serum creatinine and blood urea nitrogen are nonspecific biomarkers with insensitive and delayed response in the clinical setting. There is an urgent need to identify and qualify novel kidney safety biomarkers that would be used to detect and predict drug-induced nephrotoxicity in preclinical toxicological studies, clinical trials and patient care in sequence. To do that, eight novel renal safety biomarkers have been well characterized and qualified for preclinical drug safety screening, and their clinical bridging validation is underway as well. Of them, some are used to detect or predict proximal tubular injury, and others are used to diagnose and monitor glomerular damage. Thus, measurement of a panel of kidney safety biomarkers in parallel would help maximally capture all potential safety signals for a more informative decision to be made in drug research and development as well as for optimal selection of the drug and its dose in clinical practice.

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Source
http://dx.doi.org/10.1016/j.pharmthera.2012.09.004DOI Listing

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