Abstract
Introduction: In Denmark, it is estimated that 3-5% of children are obese. Obesity is associated with pathophysiological alterations that may lead to alterations in the pharmacokinetics of drugs. In adults, obesity was found to influence important drug-metabolising enzyme pathways. The impact of obesity-related alterations on drug metabolism and its consequences for drug dosing remains largely unknown in both children and adults. An altered drug metabolism may contribute significantly to therapeutic failure or toxicity. The aim of this trial is to investigate the in vivo activity of CYP3A4, CYP2E1 and CYP1A2 substrates in obese versus non-obese children. Methods: The CYTONOX trial is an open-label explorative pharmacokinetic trial. We intend to include 50 obese and 50 non-obese children. The primary end points are: in vivo clearance of CYP3A4, CYP2E1 and CYP1A2 substrates, which will be defined by using well-tested probes; midazolam, chlorzoxazone and caffeine. Each of the probes will be administered as a single dose. Subsequently, blood and urine samples will be collected at pre-specified times. Conclusion: The aim of the CYTONOX trial is to investigate the in vivo activity of CYP3A4, CYP2E1 and CYP1A2 in obese and non-obese children. The results are expected to be used in the future as a basis for drug dosing recommendations in obese children.
| Original language | English |
|---|---|
| Article number | A5226 |
| Journal | Danish Medical Journal |
| Volume | 63 |
| Issue number | 5 |
| Pages (from-to) | 1-5 |
| Number of pages | 5 |
| ISSN | 2245-1919 |
| Publication status | Published - May 2016 |
Keywords
- Adolescent
- Caffeine
- Child
- Chlorzoxazone
- Clinical Protocols
- Cytochrome P-450 CYP1A2
- Cytochrome P-450 CYP2E1
- Cytochrome P-450 CYP3A
- Denmark
- Female
- Humans
- Male
- Midazolam
- Pediatric Obesity
- Clinical Trial
- Journal Article
