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精神分裂症患者神经发育基因的遗传变异性检测

Genetic variability testing of neurodevelopmental genes in schizophrenic patients.

作者信息

Terzić Tea, Kastelic Matej, Dolžan Vita, Plesničar Blanka Kores

机构信息

University Psychiatric Clinic Ljubljana, Studenec 48, 1260, Ljubljana, Slovenia.

出版信息

J Mol Neurosci. 2015 May;56(1):205-11. doi: 10.1007/s12031-014-0482-5. Epub 2014 Dec 23.

Abstract

This study investigated the associations between single nucleotide polymorphisms in the neurodevelopmental Disrupted In Schizophrenia 1 (DISC1 ), neuregulin 1 (NRG1), brain-derived neurotrophic factor (BDNF) and NOTCH4 genes and the clinical symptoms and the occurrence of treatment-resistant schizophrenia in the Slovenian population. We included 138 schizophrenia patients, divided into treatment-responsive and treatment-resistant group and 94 healthy blood donors. All subjects were genotyped for eight polymorphisms (DISC1 rs6675281, DISC1 rs821616, NRG1 rs3735781, NRG1 rs3735782, NRG1 rs10503929, NRG1 rs3924999, BDNF rs6265, NOTCH rs367398) and investigated for associations with clinical variables. NOTCH4 rs367398 AA/AG was significantly associated with worse Positive and Negative Syndrome Scale (PANSS) and Clinical Global Impression (CGI) score. NOTCH4 rs367398 was not statistically significantly associated with the occurrence of treatment-resistant schizophrenia after the correction for multiple testing. Our data indicate that NOTCH4 polymorphism can influence clinical symptoms in Slovenian patients with schizophrenia.

摘要

本研究调查了精神分裂症相关基因1(DISC1)、神经调节蛋白1(NRG1)、脑源性神经营养因子(BDNF)和NOTCH4基因中的单核苷酸多态性与斯洛文尼亚人群中精神分裂症临床症状及难治性精神分裂症发生之间的关联。我们纳入了138例精神分裂症患者,分为治疗反应性组和难治性组,以及94名健康献血者。对所有受试者的8个多态性位点(DISC1 rs6675281、DISC1 rs821616、NRG1 rs3735781、NRG1 rs3735782、NRG1 rs10503929、NRG1 rs3924999、BDNF rs6265、NOTCH rs367398)进行基因分型,并研究其与临床变量的关联。NOTCH4 rs367398 AA/AG与较差的阳性和阴性症状量表(PANSS)及临床总体印象(CGI)评分显著相关。在进行多重检验校正后,NOTCH4 rs367398与难治性精神分裂症的发生无统计学显著关联。我们的数据表明,NOTCH4多态性可影响斯洛文尼亚精神分裂症患者的临床症状。

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