CYP2D6

Liver enzyme variant

CYP2D6 is a liver enzyme that metabolizes roughly a quarter of all prescription drugs, including many antidepressants, opioids, and heart medications.

Genetic variations in CYP2D6 cause people to metabolize these drugs at different rates—poor metabolizers may experience toxic buildup, while ultra-rapid metabolizers may get no therapeutic effect from standard doses.

Pharmacogenetic testing for CYP2D6 status increasingly guides prescribing decisions.

pharmacogenomics

drug metabolism

Body's chemical processing of medications

tamoxifen · antidepressants · opioids · pharmacokinetics · dosing · adverse reactions · clinical guidelines · precision medicine

biochemistry

enzyme

Protein that hastens reactions

inhibitor · inducer · dextromethorphan · metabolism · heme · active site · catalysis · biotransformation · Michaelis-Menten

genetics

polymorphism

Many forms, one interface

duplication · haplotype · heterozygous · homozygous · wild-type · genotyping · PCR · sequencing · inheritance · genetic testing

clinical

drug interaction

Substances altering each other's effects

quinidine · inhibition · psychiatric medication · pain management · oncology · breast cancer · morphine · hydrocodone · tramadol · arrhythmia

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