Takekita Yoshiteru, Fabbri Chiara, Kato Masaki, Koshikawa Yosuke, Tajika Aran, Kinoshita Toshihiko, Serretti Alessandro
Department of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna, Italy (Drs Takekita, Fabbri, and Serretti); Department of Neuropsychiatry, Kansai Medical University, Osaka, Japan (Drs Takekita, Kato, Koshikawa, and Kinoshita); Department of Health Promotion and Human Behavior, Kyoto University Graduate School of Medicine/School of Public Health, Kyoto, Japan (Dr Tajika).
Int J Neuropsychopharmacol. 2016 Apr 29;19(5). doi: 10.1093/ijnp/pyv125. Print 2016 May.
This meta-analysis was conducted to evaluate whether HTR1A gene polymorphisms impact the efficacy of antipsychotic drugs in patients with schizophrenia.
Candidate gene studies that were published in English up to August 6, 2015 were identified by a literature search of PubMed, Web of Science, and Google scholar. Data were pooled from individual clinical trials considering overall symptoms, positive symptoms and negative symptoms, and standard mean differences were calculated by applying a random-effects model.
The present meta-analysis included a total of 1281 patients from 10 studies. Three polymorphisms of HTR1A (rs6295, rs878567, and rs1423691) were selected for the analysis. In the pooled data from all studies, none of these HTR1A polymorphisms correlated significantly with either overall symptoms or positive symptoms. However, C allele carriers of the rs6295 polymorphism showed a significantly greater negative symptoms improvement than G allele carriers (P=.04, standardized mean difference =-0.14, 95%CI = 0.01 to 0.28).
The results of our present analysis indicate that the HTR1A rs6295 polymorphism may impact negative symptoms improvement but not on either overall symptoms or positive symptoms improvement. However, this meta-analysis was based on a small number of studies and patients, and the effect size on negative symptoms was small. Given this limitation, the results should be confirmed by further investigations.
本荟萃分析旨在评估5-羟色胺受体1A(HTR1A)基因多态性是否影响精神分裂症患者使用抗精神病药物的疗效。
通过检索PubMed、科学网和谷歌学术,确定截至2015年8月6日发表的英文候选基因研究。从各项临床试验中汇总数据,考虑总体症状、阳性症状和阴性症状,并采用随机效应模型计算标准平均差。
本荟萃分析共纳入来自10项研究的1281例患者。选择HTR1A的三种多态性(rs6295、rs878567和rs1423691)进行分析。在所有研究的汇总数据中,这些HTR1A多态性均与总体症状或阳性症状无显著相关性。然而,rs6295多态性的C等位基因携带者的阴性症状改善明显大于G等位基因携带者(P = 0.04,标准化平均差=-0.14,95%CI = 0.01至0.28)。
我们目前的分析结果表明,HTR1A rs6295多态性可能影响阴性症状的改善,但不影响总体症状或阳性症状的改善。然而,本荟萃分析基于少量的研究和患者,对阴性症状的效应量较小。鉴于这一局限性,结果应通过进一步研究加以证实。