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首发精神分裂症治疗的药物遗传学:D3和5-HT2C受体基因多态性分别与阳性和阴性症状反应相关。

Pharmacogenetics of treatment in first-episode schizophrenia: D3 and 5-HT2C receptor polymorphisms separately associate with positive and negative symptom response.

作者信息

Reynolds Gavin P, Yao Zhijian, Zhang XiaoBin, Sun Jing, Zhang ZhiJun

机构信息

Department of Mental Health, Queen's University Belfast, Whitla Medical Building, 97 Lisburn Road, Belfast BT9 7BL, UK.

出版信息

Eur Neuropsychopharmacol. 2005 Mar;15(2):143-51. doi: 10.1016/j.euroneuro.2004.07.001.

Abstract

We have been studying the pharmacogenetic correlates of side effects and early response to antipsychotic treatment in a series of Chinese Han first-episode drug-naive patients with schizophrenia. Here, we report the association of three functional polymorphisms of receptor genes on initial symptom severity and outcome in these patients. We studied the dopamine D3 receptor ser9gly, the dopamine D2 receptor Taq IA and the 5-HT2C receptor promoter -759C/T polymorphisms in 117 patients who had symptoms assessed by Positive and Negative Syndrome Scale (PANSS) on admission and following 10-week antipsychotic treatment, primarily with risperidone or chlorpromazine. The D2 polymorphism was found not to be significantly associated with baseline levels or changes in total PANSS in these patients. The D3 genotype is associated with the change in total PANSS (p<0.01), an effect reflecting positive and general (each p<0.01) but not negative symptom improvement. However, symptom improvement at 10 weeks strongly correlates with total PANSS score on admission, in which the greater improvement is seen with the more severe initial symptom score. The D3 genotype is also related to severity on admission, i.e. to total baseline PANSS (p<0.05), including baseline PANSS score as a covariate, the association of the genotype to change over 10 weeks remains significant for total PANSS (p<0.05) and for positive and general, but not negative, symptom scores. The 5-HT2C promoter polymorphism was also associated with improvement in PANSS (p<0.05), but reflecting effects on negative and general, but not positive, symptom scores. This polymorphism was not associated with PANSS score on admission, although after controlling for the effect of this parameter on 10-week outcome, a stronger association with change in total PANSS (p<0.01) was apparent, again reflecting improvements in negative and general symptoms but not changes in positive symptoms.

摘要

我们一直在研究一系列首次发病、未服用过药物的中国汉族精神分裂症患者对抗精神病药物治疗的副作用及早期反应的药物遗传学相关性。在此,我们报告这些患者中受体基因的三种功能多态性与初始症状严重程度及治疗结果的关联。我们研究了117例患者的多巴胺D3受体ser9gly、多巴胺D2受体Taq IA以及5 - HT2C受体启动子 - 759C/T多态性,这些患者在入院时及接受为期10周的抗精神病药物治疗(主要使用利培酮或氯丙嗪)后,通过阳性与阴性症状量表(PANSS)对症状进行评估。发现D2多态性与这些患者的PANSS总分基线水平或变化无显著关联。D3基因型与PANSS总分的变化相关(p<0.01),这一效应反映了阳性症状和一般症状(各p<0.01)的改善,但阴性症状无改善。然而,10周时的症状改善与入院时的PANSS总分密切相关,初始症状评分越严重,改善越明显。D3基因型也与入院时的严重程度相关,即与PANSS总分基线相关(p<0.05),将基线PANSS评分作为协变量,该基因型与10周内变化的关联在PANSS总分(p<0.05)以及阳性和一般症状评分方面仍然显著,但阴性症状评分无此关联。5 - HT2C启动子多态性也与PANSS的改善相关(p<0.05),但反映的是对阴性和一般症状评分的影响,而非阳性症状评分。该多态性与入院时的PANSS评分无关,尽管在控制该参数对10周治疗结果的影响后,与PANSS总分变化的更强关联(p<0.01)变得明显,再次反映了阴性和一般症状的改善,而非阳性症状的变化。

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