The coding-synonymous polymorphism rs1045280 (Ser280Ser) in β-arrestin 2 (ARRB2) gene is associated with tardive dyskinesia in Chinese patients with schizophrenia

Background:  Tardive dyskinesia (TD) is a severe and potentially irreversible adverse effect of long‐term antipsychotic treatment. Typical antipsychotics are commonly binding to the dopamine receptor D2 (DRD2), but the occurrence of antipsychotic‐induced TD is rather delayed; therefore, the developm...

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Veröffentlicht in:European journal of neurology 2008-12, Vol.15 (12), p.1406-1408
Hauptverfasser: Liou, Y.-J., Wang, Y.-C., Chen, J.-Y., Chen, M.-L., Chen, T.-T., Bai, Y.-M., Lin, C.-C., Liao, D.-L., Lai, I.-C.
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Sprache:eng
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Zusammenfassung:Background:  Tardive dyskinesia (TD) is a severe and potentially irreversible adverse effect of long‐term antipsychotic treatment. Typical antipsychotics are commonly binding to the dopamine receptor D2 (DRD2), but the occurrence of antipsychotic‐induced TD is rather delayed; therefore, the development of TD may be associated with mediators or signalling complexes behind DRD2, such as β‐arrestin 2 (ARRB2), an important mediator between DRD2 and serine–threonine protein kinase (AKT) signal cascade. Methods:  A case–control study to evaluate the association between rs1045280 (Ser280Ser) and antipsychotic‐induced TD was performed amongst 381 patients (TD/non‐TD = 228/153). Results:  There was a significant difference in the genotype distribution between TD and non‐TD groups (P = 0.025); furthermore, the allelic analysis indicated that patients with T allele had increased risk of TD occurrence (ORT = 1.58, 95% CI = 1.14–2.19, P = 0.007). Conclusions:  To the best of our knowledge, this is the first study reporting a positive association between the SNP rs1045280 and TD in schizophrenic patients.
ISSN:1351-5101
1468-1331
1471-0552
DOI:10.1111/j.1468-1331.2008.02316.x