首页> 外文期刊>British journal of clinical pharmacology >Association between 8 P‐glycoprotein (MDR1/ABCB1) gene polymorphisms and antipsychotic drug‐induced hyperprolactinaemia
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Association between 8 P‐glycoprotein (MDR1/ABCB1) gene polymorphisms and antipsychotic drug‐induced hyperprolactinaemia

机译:8 p-糖蛋白(MDR1 / ABCB1)基因多态性和抗精神病药诱导的高丙基血症之间的关联

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Introduction Hyperprolactinaemia, a common adverse effect of antipsychotic drugs, is primarily linked to blockade of dopamine D2 receptors in the pituitary gland. Certain antipsychotic drugs, such as, for example risperidone and paliperidone, are more likely to induce hyperprolactinaemia compared to others. This effect is probably caused by a relatively high blood/brain concentration ratio, a consequence of being a substrate of P‐glycoprotein. Genetic variants of P‐glycoprotein with changed functional activity might influence the potential of risperidone and paliperidone to cause hyperprolactinaemia as the altered blood/brain concentration ratio would lead to a reduced therapeutic drug level within essential brain areas making dose adaptations necessary. This increases exposure of dopamine D2 receptors within the pituitary gland. Aims To investigate possible associations between MDR1/ABCB1 gene polymorphisms and antipsychotic drug‐induced hyperprolactinaemia in Russian patients with schizophrenia and to determine possible differences between risperidone/paliperidone and other antipsychotics. Methods In total, 446 patients with schizophrenia were included from 3 psychiatric hospitals in Siberia. Blood samples were obtained in a cross‐sectional study design for DNA extraction and prolactin measurement. Associations between hyperprolactinaemia and 8 MDR1/ABCB1 gene‐polymorphisms were assessed using logistic regression analysis accounting for covariates. The analysis was repeated in a patient subgroup using risperidone or paliperidone. Results We did not observe an association between any of the 8 single nucleotide polymorphisms and the prevalence of antipsychotic‐induced hyperprolactinaemia in the total patient population. However, in the risperidone/paliperidone subgroup, the single nucleotide polymorphism rs2032582 (G2677T) was found to be negatively associated with risperidone/paliperidone‐induced hyperprolactinaemia. Conclusion This study revealed a significant association between the ABCB1 gene polymorphism rs2032582 (G2677T) and risperidone/paliperidone‐induced hyperprolactinaemia.
机译:引言过脱硫血症,抗精神病药物的常见不良影响,主要与垂体腺体中的多巴胺D2受体封闭。某些抗精神病药物,例如Risperidone和paliperidone,与他人相比,更可能诱导高丙酰胺血症。这种效果可能是由相对高的血液/脑浓度比引起的,这是p-糖蛋白的基材。 P-糖蛋白的遗传变异与变化的功能活性可能会影响利培酮和Paliperidone的潜力,导致高丙基菌血症因为改变的血液/脑浓度比率导致必要的脑区域内的治疗药物水平降低,使得必要的剂量适应。这增加了垂体腺内的多巴胺D2受体暴露。旨在调查MDR1 / ABCB1基因多态性和抗精神病药诱导的俄罗斯精神分裂症患者的可能的关联,并确定Risperidone / paliperidone和其他抗精神病学之间可能的差异。共有446例精神分裂症患者的方法包括来自西伯利亚的3名精神科医院。在横截面研究设计中获得血液样品进行DNA提取和催乳素测量。利用逻辑回归分析对协变量进行评估,评估过术血症和8mdr1 / ABCB1基因多态性之间的关联。使用Risperidone或Paliperidone在患者亚组中重复分析。结果我们没有观察到8种单核苷酸多态性中的任何一种与抗精神病药诱导的高患者血症的患病率之间的任何关联。然而,在丙酮酮/求甲酮亚组中,发现单个核苷酸多态性RS2032582(G2677T)与立妥酮/求助酮诱导的高丙基癌血症负相关。结论本研究揭示了ABCB1基因多态性RS2032582(G2677T)和立苯胺/求助酮诱导的高丙酰胺血症的重要关联。

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