Suppr超能文献

TAAR6变异对精神分裂症住院患者样本的临床表现及预后的影响:一项开放性标签研究。

TAAR6 variation effect on clinic presentation and outcome in a sample of schizophrenic in-patients: an open label study.

作者信息

Pae Chi-Un, Drago Antonio, Kim Jung-Jin, Patkar Ashwin A, Jun Tae-Youn, Lee Chul, Mandelli Laura, De Ronchi Diana, Paik In-Ho, Serretti Alessandro

机构信息

Department of Psychiatry, Kangnam St. Mary's Hospital, The Catholic University of Korea College of Medicine, Seoul, Republic of Korea.

出版信息

Eur Psychiatry. 2008 Sep;23(6):390-5. doi: 10.1016/j.eurpsy.2008.04.004. Epub 2008 Jun 25.

Abstract

We recently reported an association between TAAR6 (trace amine associated receptor 6 gene) variations and schizophrenia (SZ). We now report an association of a set of TAAR6 variations and clinical presentation and outcome in a sample of 240 SZ Korean patients. Patients were selected by a Structured Clinical Interview, DSM-IV Axis I disorders - Clinical Version (SCID-CV). Other psychiatric or neurologic disorders, as well as medical diseases, were exclusion criteria. To assess symptom severity, patients were administered the CGI scale and the PANSS at baseline and at the moment of discharge, 1 month later on average. TAAR6 variations rs6903874, rs7452939, rs8192625 and rs4305745 were investigated; rs6903874, rs7452939 and rs8192625 entered the statistical investigation after LD analysis. Rs8192625 G/G homozygosis was found to be significantly associated both with a worse clinical presentation at PANSS total and positive scores and with a shorter period of illness before hospitalization. No haplotype significant findings were found. The present study stands for a role of the TAAR6 in the clinical presentation of SZ. Moreover, our results show that this genetic effect may be counteracted by a correct treatment. Haplotype analysis was not informative in our sample, probably also because of the incomplete SNPs' coverage of the gene we performed. Further studies in this direction are warranted.

摘要

我们最近报告了痕量胺相关受体6基因(TAAR6)变异与精神分裂症(SZ)之间的关联。现在,我们报告在240例韩国SZ患者样本中,一组TAAR6变异与临床表现及预后的关联。患者通过结构化临床访谈、DSM-IV轴I障碍临床版(SCID-CV)进行筛选。其他精神或神经疾病以及内科疾病均为排除标准。为评估症状严重程度,在基线时以及出院时(平均1个月后)对患者进行临床总体印象量表(CGI)和阳性与阴性症状量表(PANSS)评定。对TAAR6变异rs6903874、rs7452939、rs8192625和rs4305745进行研究;rs6903874、rs7452939和rs8192625在连锁不平衡分析后进入统计学研究。发现rs8192625 G/G纯合子与PANSS总分及阳性评分较差的临床表现以及住院前病程较短均显著相关。未发现单倍型有显著结果。本研究表明TAAR6在SZ临床表现中起作用。此外,我们的结果表明这种遗传效应可能会被正确的治疗所抵消。单倍型分析在我们的样本中未提供有用信息,可能也是因为我们对该基因的单核苷酸多态性(SNP)覆盖不完全。有必要在这个方向上进行进一步研究。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验