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首页> 外文期刊>Human psychopharmacology: clinical and experimental >The relationship between the serotonin 2A receptor gene –1438A/G and 102T/C polymorphisms and citalopram/sertraline‐induced nausea in major depressed patients
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The relationship between the serotonin 2A receptor gene –1438A/G and 102T/C polymorphisms and citalopram/sertraline‐induced nausea in major depressed patients

机译:5 -羟色胺2 a受体之间的关系基因-1438 a / G和102 t / C多态性西酞普兰和舍曲林感应恶心主要抑郁症患者

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Abstract Objective The aim of the present study was to determine the relationship between the polymorphisms of –1438A/G and 102T/C in the 5‐HT2A receptor (HTR2A) gene and nausea/vomiting as a side effect induced by sertraline (SERT) or citalopram (CIT) in patients with major depressive disorder. Methods A total of 128 patients were enrolled, 63 patients received CIT, whereas 65 patients were treated with SERT. Nausea/vomiting were assessed with the UKU Side‐effects Rating Scale at baseline and at the end of the second and fourth weeks. Polymerase chain reaction‐restriction fragment length polymorphism technique was employed to determine genetic differences. Results We have found that, in the patients treated with CIT, there was a nominally significant difference in the genotypic distribution associated with ‐1438A/G polymorphism between patients with and without nausea ( X 2 ? = ?6.15 , p?= ?0.041). Moreover, logistic regression analysis revealed a significant association between nausea/vomiting as a side effect and –1438A/G polymorphism. That is, patients with the G allele were at a higher risk for developing nausea/vomiting ( p?= ?0.044 , odds ratio?=?2.213). The 102T/C polymorphism in the HTR2A gene had no significant effect on the nausea/vomiting as a side effect among participants treated with either CIT or SERT. Conclusion The present study suggests the association of the HTR2A gene –1438A/G polymorphism with nausea/vomiting as a side effect related to CIT treatment.
机译:摘要目的本研究的目的是确定之间的关系-1438 a / G多态性和102 t / C5 HT2A受体(HTR2A)基因和恶心/呕吐作为舍曲林(泽特)或引起的副作用西酞普兰(CIT)患者的专业抑郁障碍。患者注册,63名患者接受CIT,而65名患者接受泽特。恶心/呕吐与UKU进行评估方评定量表在基线和量的影响第二和第四个星期。连锁反应的限制片段长度多态性技术来确定遗传差异。患者在CIT,在基因型的名义上的显著差异分布与1438 a / G患者之间的多态性恶心(X 2 ?logistic回归分析显示恶心/呕吐之间的显著联系作为一个副作用和-1438 a / G多态性。是,患者G等位基因在更高吗发病的恶心/呕吐(p ?2.213,比值比? = ?)。HTR2A基因没有显著的影响恶心/呕吐的副作用之一参与者对待CIT或泽特。结论本研究表明协会的HTR2A基因-1438 a / G多态性与恶心/呕吐的一面CIT治疗效果相关。

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