2012•Encyclopedia of Drug Metabolism and InteractionsRequires access

Clinical Implications of CYP Induction‐Mediated Drug–Drug Interactions

Jiunn Huei Lin, Jianjun Guo

Open publisher page 0 citations

Abstract

Abstract Cytochrome P450 (CYP) induction‐mediated drug interaction is a major concern in clinical practice. Although the reported cases of CYP induction‐mediated drug interactions are less frequent than that of CYP inhibition‐mediated drug interactions, there are two major concerns with CYP induction. First, induction may cause a reduction in therapeutic efficacy as a result of increased drug metabolism. Second, induction may create an undesirable imbalance between bioactivation and detoxification as a result of increased formation of reactive metabolites leading to an increase in the risk of metabolite‐induced toxicity. Therefore, CYP induction has been considered as an important factor for consideration during drug discovery and development. The purpose of this chapter is to review the effects of CYP induction on pharmacokinetics of drugs and its clinical implications.

About this research paper

What this paper is about

Abstract Cytochrome P450 (CYP) induction‐mediated drug interaction is a major concern in clinical practice. Although the reported cases of CYP induction‐mediated drug interactions are less frequent than that of CYP inhibition‐mediated drug interactions, there are two major concerns with CYP induction. First, induction may cause a reduction in therapeutic efficacy as a result of increased drug metabolism. Second, induction may create an undesirable imbalance between bioactivation and detoxification as a result of increased formation of reactive metabolites leading to an increase in the risk of metabolite‐induced toxicity. Therefore, CYP induction has been considered as an important factor for consideration during drug discovery and development. The purpose of this chapter is to review the effects of CYP induction on pharmacokinetics of drugs and its clinical implications.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract Cytochrome P450 (CYP) induction‐mediated drug interaction is a major concern in clinical practice. Although the reported cases of CYP induction‐mediated drug interactions are less frequent than that of CYP inhibition‐mediated drug interactions, there are two major concerns with CYP induction. First, induction may cause a reduction in therapeutic efficacy as a result of increased drug metabolism. Second, induction may create an undesirable imbalance between bioactivation and detoxification as a result of increased formation of reactive metabolites leading to an increase in the risk of metabolite‐induced toxicity. Therefore, CYP induction has been considered as an important factor for consideration during drug discovery and development. The purpose of this chapter is to review the effects of CYP induction on pharmacokinetics of drugs and its clinical implications.

Key concepts: Drug, Cytochrome P450, Pharmacology, Drug metabolism, Metabolite, Pharmacokinetics, Drug development, Drug interaction

Related papers

Back to paper searchBrowse research topicsOriginal source
Clinical Implications of CYP Induction‐Mediated Drug–Drug Interactions — Research Paper | ScholarLens