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多巴胺(DRD2)和5-羟色胺(HTR2A、2C)受体基因多态性不影响南印度精神分裂症患者对利培酮的早期反应。

Dopamine (DRD2) and Serotonin (HTR2A, 2C) Receptor Gene Polymorphisms do not influence early response to Risperidone in South Indian Patients with Schizophrenia.

作者信息

Alladi Charanraj Goud, RajKumar Ravi Philip, Adithan Surendiran, Marie-Claire Cynthia, Bellivier Frank, Shewade Deepak Gopal

机构信息

Department of Pharmacology, Jawaharlal Institute of Post-graduate Medical Education and Research, Puducherry, 605006, India.

Inserm, U1144, Paris, F-75006, France.

出版信息

Fundam Clin Pharmacol. 2019 Jun;33(3):355-364. doi: 10.1111/fcp.12424. Epub 2018 Nov 21.

Abstract

Treatment response to antipsychotic drugs is variable and conflicting results have been obtained while studying the influence of DRD2 and HTR2 genetic variants on antipsychotic drug efficacy. To explore further, the present study aimed to assess the influence of DRD2 -141 C Ins/Del, Taq1A and HTR2A -1438 G/A, 102T/C and HTR2C -759 C/T genetic polymorphisms in response to risperidone in patients with schizophrenia. The study was conducted among the n = 320 South Indian patients with schizophrenia who received risperidone treatment (4-8 mg per day) for a minimum of four weeks. Genotyping was done by real-time PCR. Antipsychotic response was assessed using CGI-I score in cross-sectional group, PANSS score in prospective group at baseline and after receiving the risperidone therapy. DRD2 -141 C Ins/Del (n = 310, Ins/Ins = 177, Ins/Del+ Del/Del = 133, OR 0.70, 95% CI 0.4-1.2 p 0.2), Taq1A (n = 320, AA = 35, AG = 132, GG = 153, p 0.2), HTR2A -1438 G/A (n = 320, AA = 39, AG = 164, GG = 117, p 0.2), HTR2A 102T/C (n = 320, CC = 115, CT = 165, TT = 40, p 0.1) HTR2C -759 C/T (females n = 132, CC = 65, CT+TT = 67, OR 1.3, 95% CI 0.6-2.8, p 0.5; males n = 186, C = 120, T = 66, OR 1.2, 95% CI 0.6-2.4, p 0.4) genetic polymorphisms did not show any association with antipsychotic response to risperidone. DRD2 -141 C Ins/Del, Taq1A, HTR2A -1438 G/A, 102T/C and HTR2C -759 C/T genetic variants are not associated with antipsychotic response to risperidone.

摘要

抗精神病药物的治疗反应存在差异,在研究DRD2和HTR2基因变异对抗精神病药物疗效的影响时,得到的结果相互矛盾。为了进一步探究,本研究旨在评估DRD2 -141 C Ins/Del、Taq1A以及HTR2A -1438 G/A、102T/C和HTR2C -759 C/T基因多态性对精神分裂症患者使用利培酮治疗反应的影响。该研究在320名南印度精神分裂症患者中进行,这些患者接受利培酮治疗(每天4 - 8毫克)至少四周。通过实时聚合酶链反应进行基因分型。使用CGI - I评分评估横断面组的抗精神病反应,使用PANSS评分评估前瞻性组在基线和接受利培酮治疗后的抗精神病反应。DRD2 -141 C Ins/Del(n = 310,Ins/Ins = 177,Ins/Del + Del/Del = 133,OR 0.70,95% CI 0.4 - 1.2,p 0.2)、Taq1A(n = 320,AA = 35,AG = 132,GG = 153,p 0.2)、HTR2A -1438 G/A(n = 320,AA = 39,AG = 164,GG = 117,p 0.2)、HTR2A 102T/C(n = 320,CC = 115,CT = 165,TT = 40,p 0.1)、HTR2C -759 C/T(女性n = 132,CC = 65,CT + TT = 67,OR 1.3,95% CI 0.6 - 2.8,p 0.5;男性n = 186,C = 120,T = 66,OR 1.2,95% CI 0.6 - 2.4,p 0.4)基因多态性与利培酮的抗精神病反应均无关联。DRD2 -141 C Ins/Del、Taq1A、HTR2A -1438 G/A、102T/C和HTR2C -759 C/T基因变异与利培酮的抗精神病反应无关。

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