A short-term high fat diet increases exposure to midazolam and omeprazole in healthy subjects

Roos Achterbergh, Laureen A Lammers, Samuel van Nierop, Heinz-Josef Klümpen, Maarten R Soeters, Ron A A Mathôt, Johannes A Romijn

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

OBJECTIVES: Knowledge of factors contributing to variation in drug metabolism is of vital importance to optimize drug treatment. This study assesses the effects of a short-term hypercaloric high fat diet on metabolism of five oral drugs, which are each specific for a single P450 isoform: midazolam (CYP3A4), omeprazole (CYP2C19), metoprolol (CYP2D6), S-warfarin (CYP2C9) and caffeine (CYP1A2).

METHODS: In 9 healthy volunteers, pharmacokinetics of the five drugs were assessed after an overnight fast at two separate occasions: after a regular diet and after 3 days of a hypercaloric high fat diet (i.e. regular diet supplemented with 500 mL cream [1715 kcal, 35% fat]). Pharmacokinetic parameters (mean [SEM]) were estimated by non-compartmental analysis.

RESULTS: The high fat diet increased exposure to midazolam by 19% from 24.7 (2.6) to 29.5 (3.6) ng ml-1h-1 (p=0.04) and exposure to omeprazole by 31% from 726 (104) to 951 (168) ng ml-1h-1 (p=0.05). Exposure to metoprolol, caffeine and S-warfarin was not affected by the high fat diet.

CONCLUSION: A short-term hypercaloric high fat diet increases exposure to midazolam and omeprazole, possibly reflecting modulation of CYP3A4 and CYP2C19.

Original languageEnglish
Pages (from-to)715-20
Number of pages6
JournalExpert Opinion on Drug Metabolism and Toxicology
Volume12
Issue number7
DOIs
Publication statusPublished - Jul 2016
Externally publishedYes

Keywords

  • Adult
  • Cross-Over Studies
  • Cytochrome P-450 CYP2C19/metabolism
  • Cytochrome P-450 CYP3A/metabolism
  • Cytochrome P-450 Enzyme System/metabolism
  • Diet, High-Fat
  • Humans
  • Male
  • Midazolam/administration & dosage
  • Omeprazole/administration & dosage
  • Young Adult

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