Benign Prostatic Hyperplasia (BPH) PGx Test

Test Description

The Benign Prostatic Hyperplasia (BPH) PGx Test is intended for individuals undergoing treatment for benign prostatic hyperplasia or associated lower urinary tract symptoms who may benefit from personalized pharmacogenetic-guided therapy. This panel evaluates clinically relevant genetic variants in the CYP2D6 gene that may influence the metabolism, efficacy, and tolerability of medications commonly prescribed for BPH management, including tamsulosin and mirabegron. Individuals with altered CYP2D6 metabolism may experience differences in drug response or increased risk for adverse effects, and pharmacogenetic testing may help guide medication selection and dose optimization to improve therapeutic outcomes.

Ordering Information

Turnaround Time: 3-7 business days
Preferred specimens: Saliva
Alternate specimens: Buccal Swab

Testing Kit Request Form


Clinical Description

Medications used to manage benign prostatic hyperplasia, including alpha-blockers and 5-alpha reductase inhibitors, may demonstrate variability in efficacy and tolerability among individuals. Genetic differences affecting drug metabolism and receptor response can contribute to this variability. Pharmacogenomic testing may support more precise medication selection and dosing, helping to improve symptom control and reduce adverse effects.


Panel Information
MedicationGene
Tamsulosin, MirabegronCYP2D
Frequency of Cytochrome P450 (CYP2D6) Metabolizer Types in the Population
CytochromePoor metabolizerIntermediate metabolizerNormal metabolizerRapid or ultra-rapid metabolizer
CYP2D64-7%9-35%50-90%2-3%

Tagged Genes

Primary panel:

1 genes selected


References