Abstract |
Tardive dyskinesia is a severe debilitating movement disorder characterized by choreoathetotic movements developing in one-fifth of the patients with schizophrenia. In this study we have investigated the significance of CYP3A4*1B and CYP2D6*4 polymorphisms in TD susceptibility among chronic schizophrenia patients (n = 335) from north India. Tardive dyskinesia was diagnosed in approximately 29% (96/335) of these patients. No significant association of either of the two SNPs with TD ( CYP3A4*1B chi2 = 0. 308, df = 1, p = 0.579; CYP2D6*4 chi2 = 0.006, df = 1, p = 0.935) was observed. However a trend towards increased severity of TD in patients heterozygous for the CYP2D6*4 mutation was observed.
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Authors | Arun K Tiwari, Smita N Deshpande, A R Rao, Triptish Bhatia, Bernard Lerer, Vishwajit L Nimgaonkar, B K Thelma |
Journal | Schizophrenia research
(Schizophr Res)
Vol. 75
Issue 1
Pg. 21-6
(Jun 01 2005)
ISSN: 0920-9964 [Print] Netherlands |
PMID | 15820320
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antipsychotic Agents
- Cytochrome P-450 Enzyme System
- CYP3A protein, human
- Cytochrome P-450 CYP2D6
- Cytochrome P-450 CYP3A
- CYP3A4 protein, human
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Topics |
- Analysis of Variance
- Antipsychotic Agents
(adverse effects)
- Asian People
(genetics)
- Case-Control Studies
- Cross-Sectional Studies
- Cytochrome P-450 CYP2D6
(genetics)
- Cytochrome P-450 CYP3A
- Cytochrome P-450 Enzyme System
(genetics)
- Dyskinesia, Drug-Induced
(ethnology, genetics)
- Genetic Predisposition to Disease
(ethnology, genetics)
- Humans
- India
(epidemiology)
- Pharmacogenetics
- Polymorphism, Single Nucleotide
- Retrospective Studies
- Schizophrenia
(drug therapy)
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