Precise, personalized therapy    

Identify drug-gene interactions to maximize medicine

Pharmacogenomics (PGx) is a rapidly evolving field with the potential to affect every patient, everywhere. Studies suggest most individuals possess at least one actionable genetic variant that predisposes drug response. Establishing patients' genetic profiles allows physicians to select patient-specific medications that optimize therapeutic efficacy while avoiding adverse drug reactions.

Therapeutic areas impacted by PGx

  • Analgesic/Anesthesiology
  • Anti-inflammatory
  • Anticoagulant/Antiplatelet
  • Cardiovascular
  • Gastroenterology
  • Immunosuppressive
  • Infectious Disease
  • Neurology
  • Oncology
  • Psychiatry
  • Rheumatology
  • Urology

Paving the way for PGx implementation

The Molecular Technologies Laboratory at Mayo Clinic develops and validates PGx testing in partnership with the Center for Individualized Medicine and the Schulze Center for Novel Therapeutics. Evaluations include actionable genes with a high level of clinical evidence. Categorization of medication recommendations by drug class and reference source ensures easy interpretations for all audiences. 

The right drug for the right patient at the right dose

A comprehensive resource for ordering, interpreting, and understanding PGx testing. Indications for pharmacogenomic testing may include:

  • Multiple failed therapies
  • Polypharmacy cases
  • Prescription risk for hypersensitivity reactions
  • Family history of medication intolerance
  • Symptoms suggestive of drug metabolism concern
  • Severe diseases
  • Elderly and pediatric patients who have difficulty communicating adverse drug reactions

Comprehensive PGx panels

PSYQP | Psychotropic Pharmacogenomics Gene Panel, Varies

  • Examines 23 genes (141 alleles) used to assess approximately 80 medications.
  • Identifies variations in genes known to be associated with response and/or risk of toxicity with psychotropic medications.

PGXQP  | Focused Pharmacogenomics Panel, Varies

  • Examines 10 genes (82 alleles) used to assess approximately 55 medications.
  • Delivers preemptive or reactive genotyping of patients for pharmacogenetics purposes.
  • Provides assessments for genes with strong drug phenotype associations.

Medication Targeted Panels

Guides therapy when analyzing multiple drug interactions that fall into the same drug class or patients with polypharmacy.

Single Gene Orders

Guides therapy when evaluating single medications or genes not included in the comprehensive panels.

Learn more about how to order these tests at your institution.

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