Practitioners
Patients
Clinicians need confidence that pharmacogenetic testing provides reliable, actionable information. Modern PGx focuses on well-established CYP450 pathways — such as CYP2C19, CYP2D6 and CYP2B6 — enabling prescribers to anticipate how a patient will respond to common medicines.
From a laboratory perspective, genotyping accuracy exceeds 99% for validated variants. The crucial consideration is the strength of evidence supporting each drug–gene interaction.
For example, CYP2C19 poor metabolisers and clopidogrel is a CPIC Level A recommendation and is now referenced by NICE in cardiovascular guidance. Similarly, CYP2D6 testing is clinically relevant when selecting opioids or antidepressants, and SLCO1B1 testing can prevent statin-associated muscle toxicity.
At AttoDiagnostics, only guideline-supported interactions are reported with actionable recommendations, enabling confident prescribing decisions.
A 57-year-old patient begins simvastatin for primary prevention and soon experiences muscle pain.?Pharmacogenetic testing identifies an SLCO1B1 decreased-function phenotype, predicting elevated risk of statin-induced myopathy. Switching to rosuvastatin — which is less dependent on this pathway — maintains lipid control without adverse effects.?This supports adherence and reduces cardiovascular event risk.
99% analytical accuracy for validated variants.
Only drug–gene pairs with sufficient clinical evidence (e.g., CPIC A/B).
No — it enhances treatment decision-making, especially when response is unpredictable.
Yes — via UK-accredited labs such as AttoDiagnostics.
Patients with side effects, poor efficacy or high-risk medications (clopidogrel, simvastatin, SSRIs, codeine).
See how PGx integrates into your prescribing workflow. Book a Demo with AttoDiagnostics?Our clinical team will walk you through a real case and referral process.