The majority of renal cell carcinoma cases are detected accidentally, and often at a late stage. Could miRNAS serve as potential biomarkers for diagnosis and prognosis?
This review summarizes recent progress in isolating biomarkers which might predict which patients will have the greatest benefit from antidepressant therapy for depression and other mood disorders.
Drs. Deepak Voora and Svati Shah comment on a study published in JAMA looking at the additive benefit of a genetic risk score in predicting CV disease.
Drug-drug interactions are a serious clinical issue. This article looks at the mechanisms of interactions of selected intestinal, hepatic and renal drug transporters.
Firstline EGFR TKIs in Asians with mutation-positive NSCLC are known to improve outcomes. Dr. Maurie Markman reviews data on their use in Europeans and considers the impact on treatment protocols.
This review presents pharmacogenetic comparisons of two tyrosine kinease inhibitors which have associated risk of serious liver injury. By what mechanisms do they induce liver toxicity?
Dr. Maurie Markman comments on a study published in the Journal of Clinical Oncology demonstrating the benefit of anti-EGFR therapy in this difficult-to-treat population.
What should a personalized medicine approach be in a primary care practice? Dr. Scott Joy considers both patient and provider perspectives and their impact on the practice of medicine moving forward.
There is large variability in clinical response to statin therapy. This review examines genetic factors which may contribute to the lipid-lowering effectiveness of statins and their side effects.
Drug-drug interactions are a widely recognized cause of adverse drug reactions, but drug-gene interactions can be a potential source of ADRs as well. How common are they?
Professor Alison Motsinger-Reif of the Bioinformatics Research Center at North Carolina State University discusses how genome-wide association studies have changed research in pharmacogenomics.
A major challenge in kidney transplant is the prediction of allograft rejection and immunosuppressive drug response. What can pharmacogenomics contribute?
A Nature Genetics paper identifies rare variants that help explain heritability of hypertriglyceridemia, but the knowledge gain is only incremental. Dr. Ali Torkamani explains why.
Drug-drug interactions are a widely recognized cause of adverse drug reactions, but drug-gene interactions can be a potential source of ADRs as well. How common are they?
CYP2D6 is crucial for the metabolism of many drugs, but currently phenotyping requires administration of a probe drug. Could a urinary biomarker provide a noninvasive method of CYP2D6 phenotyping?
What insights can pharmacogenetic studies give us as to the various phenotypes of COPD and their differing responses to currently existing and future therapies?