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A Comprehensive Whole-Body Physiologically Based Pharmacokinetic Drug-Drug-Gene Interaction Model of Metformin and Cimetidine in Healthy Adults and Renally Impaired Individuals.

Nina HankeDenise TürkDominik SelzerNaoki IshiguroThomas EbnerSabrina WiebeFabian MüllerPeter StopferValerie NockThorsten Lehr
Published in: Clinical pharmacokinetics (2021)
Whole-body physiologically based pharmacokinetic models of metformin and cimetidine were built and qualified for the prediction of metformin pharmacokinetics during drug-gene interaction, drug-drug interaction, and different stages of renal disease. The model files will be freely available in the Open Systems Pharmacology model repository. Current guidelines for metformin treatment of renally impaired patients should be reviewed to avoid overdosing in CKD3 and to allow metformin therapy of CKD4 patients.
Keyphrases
  • end stage renal disease
  • chronic kidney disease
  • ejection fraction
  • newly diagnosed
  • adverse drug
  • prognostic factors
  • genome wide
  • copy number
  • emergency department
  • drug induced
  • transcription factor
  • combination therapy