Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine
- PMID: 9491814
- DOI: 10.1038/sj.mp.4000348
Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine
Abstract
Clozapine is a potent atypical antipsychotic which binds to a variety of neurotransmitter receptors including serotonin (5-HT) receptors. However, the precise neurochemical site of clozapine's therapeutic action is unknown. We hypothesize that genetic variation in the neurotransmitter receptors to which the drug binds may influence clozapine response. To test this hypothesis we genotyped a novel -1438-G/A polymorphism detected in the promoter region, and a His452Tyr polymorphism described in the coding region of the 5-HT2A receptor gene in two independent samples of clozapine-treated patients including responders and non-responders. Although the strong association between these polymorphisms and clozapine response observed in the first sample (sample I) was not statistically significant in the second sample (sample II), the results in both samples were in the same direction. Homozygosity for the allele G-1438 was higher among non-responders (56% in sample I, 43% in sample II) than in responders (28% in sample I and 32% in sample II) in both samples. Similarly, the frequency of allele Tyr452 was higher in non-responders (11% in sample I, 16% in sample II) than in responders (6% in sample I and 10% in sample II). A combined analysis of both samples showed association between both polymorphisms and clozapine response. These results provide further evidence suggesting that genetic variation at 5-HT2A receptors may influence clozapine response and strengthen the candidacy of these receptors as important therapeutic targets.
Similar articles
-
Analysis of a structural polymorphism in the 5-HT2A receptor and clinical response to clozapine.Neurosci Lett. 1996 Oct 18;217(2-3):177-8. Neurosci Lett. 1996. PMID: 8916101 Clinical Trial.
-
Meta-analysis of studies on genetic variation in 5-HT2A receptors and clozapine response.Schizophr Res. 1998 Jul 27;32(2):93-9. doi: 10.1016/s0920-9964(98)00032-2. Schizophr Res. 1998. PMID: 9713904
-
Association between clozapine response and allelic variation in 5-HT2A receptor gene.Lancet. 1995 Jul 29;346(8970):281-2. doi: 10.1016/s0140-6736(95)92168-0. Lancet. 1995. PMID: 7630250
-
[Pharmacogenetics and treatment response in schizophrenia].Encephale. 2007 Dec;33(6):954-64. doi: 10.1016/j.encep.2007.01.004. Epub 2007 Sep 4. Encephale. 2007. PMID: 18789788 Review. French.
-
Genetic predictors of therapeutic response to clozapine: current status of research.CNS Drugs. 2002;16(5):317-24. doi: 10.2165/00023210-200216050-00004. CNS Drugs. 2002. PMID: 11994021 Review.
Cited by
-
Peripheral biomarkers of treatment-resistant schizophrenia: Genetic, inflammation and stress perspectives.Front Pharmacol. 2022 Oct 12;13:1005702. doi: 10.3389/fphar.2022.1005702. eCollection 2022. Front Pharmacol. 2022. PMID: 36313375 Free PMC article. Review.
-
A Cross-Sectional Study on the Relationship Among Cytokines, 5-HT2A Receptor Polymorphisms, and Sleep Quality of Non-manual Workers in Xinjiang, China.Front Psychiatry. 2022 Apr 6;13:777566. doi: 10.3389/fpsyt.2022.777566. eCollection 2022. Front Psychiatry. 2022. PMID: 35463508 Free PMC article.
-
Genetic Testing for Antipsychotic Pharmacotherapy: Bench to Bedside.Behav Sci (Basel). 2021 Jun 30;11(7):97. doi: 10.3390/bs11070097. Behav Sci (Basel). 2021. PMID: 34209185 Free PMC article. Review.
-
Common HTR2A variants and 5-HTTLPR are not associated with human in vivo serotonin 2A receptor levels.Hum Brain Mapp. 2020 Nov;41(16):4518-4528. doi: 10.1002/hbm.25138. Epub 2020 Jul 22. Hum Brain Mapp. 2020. PMID: 32697408 Free PMC article.
-
Genetic endophenotypes for insomnia of major depressive disorder and treatment-induced insomnia.J Neural Transm (Vienna). 2019 Jun;126(6):711-722. doi: 10.1007/s00702-019-02014-y. Epub 2019 May 18. J Neural Transm (Vienna). 2019. PMID: 31111219
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
