Related Experiment Video
Updated: Mar 24, 2026

Early Detection of Drug-Induced Renal Hemodynamic Dysfunction Using Sonographic Technology in Rats
Published on: March 11, 2016
Role of Pharmacogenomics in Kidney Disease and Injury
Linda Awdishu1, Melanie S Joy1
1Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, CA; Skaggs School of Pharmacy and Pharmaceutical Sciences, Department of Pharmaceutical Sciences, University of Colorado, Aurora, CO; and Division of Renal Diseases and Hypertension, School of Medicine, Aurora, CO.
Abstract:
There has been considerable excitement in the kidney community surrounding the research findings on the genetic contributions to kidney diseases. However, positive outcomes of personalized therapeutic interventions can be circumvented by unpredictable pharmacokinetics of prescribed drugs. Furthermore, unpredictable drug disposition can result in toxicities such as kidney injury. Patient covariates, disease covariates, and pharmacogenetics all contribute to variability in drug disposition. Further treatment personalization and avoidance of drug- and biologic- induced kidney injury will require extensive knowledge and expertise in renal clinical pharmacology. The current review will focus on the pharmacogenetics of drugs and biologics used in the treatment of glomerular kidney diseases and drugs implicated in inducing kidney injury phenotypes.
Insights
Genetic factors influence kidney diseases, but drug effects vary. Understanding pharmacogenetics is key to personalized treatments and preventing drug-induced kidney injury.
Area of Science:
- Nephrology
- Clinical Pharmacology
- Genetics
Background:
- Genetic discoveries are advancing kidney disease research.
- Personalized medicine in kidney disease faces challenges due to unpredictable drug pharmacokinetics and potential toxicities like kidney injury.
- Variability in drug disposition is influenced by patient and disease factors, alongside pharmacogenetics.
Purpose of the Study:
- To review the pharmacogenetics of drugs and biologics for glomerular kidney diseases.
- To examine drugs known to cause kidney injury phenotypes.
- To highlight the importance of renal clinical pharmacology for treatment personalization and preventing drug-induced kidney injury.
Main Methods:
- Literature review of pharmacogenetic studies.
- Analysis of drug and biologic treatments for glomerular diseases.
- Examination of drug-induced kidney injury mechanisms and phenotypes.
Main Results:
- Pharmacogenetics significantly impacts drug disposition and efficacy in kidney diseases.
- Certain drugs and biologics used in glomerular diseases have known pharmacogenetic associations.
- A range of medications can precipitate kidney injury, with varying genetic predispositions.
Conclusions:
- Integrating pharmacogenetics into clinical practice is essential for optimizing kidney disease treatment.
- Personalized therapeutic strategies can mitigate risks associated with drug disposition variability.
- Further research in renal clinical pharmacology is crucial to avoid drug- and biologic-induced kidney injury.
Related Concept Videos
Pharmacogenetics and Pharmacogenomics: Overview
Pharmacogenetics of Drug Metabolism: Overview
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Pharmacogenomics: Identification of New Drug Targets
Principles of Pharmacogenetics: Types of Genetic Variants
Pharmacogenetics of Phase I Enzymes: Cytochrome P450 Isozymes

