- Lu, Justin Y;
- Tiwari, Arun K;
- Freeman, Natalie;
- Zai, Gwyneth C;
- de Luca, Vincenzo;
- Müller, Daniel J;
- Tampakeras, Maria;
- Herbert, Deanna;
- Emmerson, Heather;
- Cheema, Sheraz Y;
- King, Nicole;
- Voineskos, Aristotle N;
- Potkin, Steven G;
- Lieberman, Jeffrey A;
- Meltzer, Herbert Y;
- Remington, Gary;
- Kennedy, James L;
- Zai, Clement C
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.