J Korean Soc Biol Psychiatry.  2003 Nov;10(2):133-140.

Association between Tardive Dyskinesia and T103C Polymorphisms of 5-HT2A Receptor Gene

• Hahn SW
• Shin JW
• Choi TY
• Woo SI
• Jung HY
• Jung HY
• Han SH

Abstract

OBJECTIVE
Some candidate gene polymorphisms were reported to be associated with tardive dyskinesia (TD). The aim of this study was to investigate the association of the 5-HT2A receptor gene polymorphisms with TD in Korean schizophrenic subjects. METHOD: Subjects were of 59 schizophrenic patients with TD and 60 schizophrenic patients without TD for studying of 5-HT2A receptor gene polymorphisms. TD was evaluated using the Abnormal Involuntary Movement Scale(AIMS). Genomic DNA was amplified by PCR and digestion with MspI and BsmI. RESULT: There were no statistically significant differences in the demographic variables, such as age, male to female percentage, duration of illnesses and duration of antipsychotic drug exposure between the TD group and control group. 1) T102C polymorphisms and TD Comparing the TD group and control group, the 102T/C allele was associated with a significantly increased risk for TD (chi2=5.560, df=1, p=0.018). 2) Three AIMS categories of TD and T102C genotype. There were statistically significant differences in the three AIMS categories(chi2=6.835, df=2, p=0.033).
CONCLUSION
These result suggest 102T/C genotypes of the 5-HT2A receptor gene are related to the development of TD. The 102T/C genotypes were associated with significantly higher AIMS orofacial dyskinesia scores. These findings suggest that the 5-HT2A receptor gene is significantly associated with susceptibility to TD in patients with chronic schizophrenia.

MeSH Terms

Alleles
Digestion
DNA
Dyskinesias
Female
Genotype
Humans
Male
Movement Disorders*
Polymerase Chain Reaction
Receptor, Serotonin, 5-HT2A*
Schizophrenia
DNA
Receptor, Serotonin, 5-HT2A