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Liver enzyme CYP2D6 gene and tardive dyskinesia.

Justin Y LuArun K TiwariNatalie FreemanGwyneth C ZaiVincenzo de LucaDaniel J MüllerMaria TampakerasDeanna HerbertHeather EmmersonSheraz Y CheemaNicole KingAristotle N VoineskosSteven G PotkinJeffrey A LiebermanHerbert Y MeltzerGary RemingtonJames L KennedyClement C Zai
Published in: Pharmacogenomics (2020)
Background: Tardive dyskinesia (TD) is an iatrogenic involuntary movement disorder occurring after extended antipsychotic use with unclear pathogenesis. CYP2D6 is a liver enzyme involved in antipsychotic metabolism and a well-studied gene candidate for TD. Materials & methods: We tested predicted CYP2D6 metabolizer phenotype with TD occurrence and severity in our two samples of European chronic schizophrenia patients (total n = 198, of which 82 had TD). Results: TD occurrence were associated with extreme metabolizer phenotype, controlling for age and sex (p = 0.012). In other words, individuals with either increased and no CYP2D6 activity were at higher risk of having TD. Conclusion: Unlike most previous findings, TD occurrence may be associated with both extremes of CYP2D6 metabolic activity rather than solely for poor metabolizers.
Keyphrases
  • risk assessment
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • chronic kidney disease
  • bipolar disorder
  • copy number
  • patient reported
  • genome wide analysis