Suppr超能文献

基因(rs11030101)中的一种多态性与中国汉族精神分裂症患者的阴性症状相关。

A Polymorphism in the Gene (rs11030101) is Associated With Negative Symptoms in Chinese Han Patients With Schizophrenia.

作者信息

Ping Junjiao, Zhang Jie, Wan Jing, Huang Caiying, Luo Jiali, Du Baoguo, Jiang Tingyun

机构信息

Department of Psychiatry, The Third People's Hospital of Zhongshan City, Zhongshan, China.

Joint Laboratory of Psychiatric Genetic Research, The Third People's Hospital of Zhongshan, Zhongshan, China.

出版信息

Front Genet. 2022 Mar 16;13:849227. doi: 10.3389/fgene.2022.849227. eCollection 2022.

Abstract

This study aimed to investigate the association between brain-derived neurotrophic factor () and cyclic adenosine monophosphate response element binding protein () gene polymorphisms and schizophrenia. This study used a case-control design, and diagnoses were made based on the Diagnostic and Statistical Manual of Mental Disorders-Fifth Edition criteria. One hundred and thirty-four patients with schizophrenia were recruited from the Third People's Hospital of Zhongshan City from January 2018 to April 2020. Sixty-four healthy controls were recruited from the same region. Genotypes at the gene single nucleotide polymorphisms rs11030101, rs2030324, and rs6265 and the gene single nucleotide polymorphisms rs6740584 and rs2551640 were determined using a MassARRAY mass spectrometer. Linkage disequilibrium and haplotype analyses were performed, and genotype and allele frequencies were compared between groups. The positive and negative symptom scale (PANSS) was used to evaluate the association between the and gene polymorphisms and schizophrenic symptoms. There was no significant difference in genotype or allele frequencies for rs11030101, rs2030324, rs6265, rs6740584, or rs2551640 between schizophrenic patients and controls (p > 0.05). In addition, there were no significant differences in rs11030101, rs2030324, rs6265, rs6740584, or rs2551640 genotype frequencies between the two groups in the dominant, recessive, or over-dominant models (p > 0.05). Three loci in the BDNF gene and two loci in the CREB gene were in a state of strong linkage disequilibrium. The frequency of haplotype AAC (rs11030101/rs2030324/rs626), composed of three loci in the BDNF gene, was significantly increased in schizophrenic patients compared with control subjects. There were significant differences in the subscores of PANSSS for negative symptoms, in patients with different rs11030101 genotypes of the gene ( < 0.05). There was also significant differences in the PANSS scores for the general symptom G12 (judgment and lack of insight) in patients with different rs6265 genotypes of the gene ( < 0.05). The gene rs11030101/rs2030324/rs6265 AAC haplotype was potentially associated with an increased risk of schizophrenia. In addition, genotypes at the rs11030101 and rs6265 loci may affect the negative symptoms and general symptoms of schizophrenic patients, respectively.

摘要

本研究旨在探讨脑源性神经营养因子(BDNF)和环磷酸腺苷反应元件结合蛋白(CREB)基因多态性与精神分裂症之间的关联。本研究采用病例对照设计,诊断依据为《精神疾病诊断与统计手册(第五版)》标准。2018年1月至2020年4月,从中山市第三人民医院招募了134例精神分裂症患者。从同一地区招募了64名健康对照者。使用MassARRAY质谱仪测定BDNF基因单核苷酸多态性rs11030101、rs2030324和rs6265以及CREB基因单核苷酸多态性rs6740584和rs2551640的基因型。进行连锁不平衡和单倍型分析,并比较两组之间的基因型和等位基因频率。采用阳性和阴性症状量表(PANSS)评估BDNF和CREB基因多态性与精神分裂症症状之间的关联。精神分裂症患者与对照组之间,rs11030101、rs2030324、rs6265、rs6740584或rs2551640的基因型或等位基因频率无显著差异(p>0.05)。此外,在显性、隐性或超显性模型中,两组之间rs11030101、rs2030324、rs6265、rs6740584或rs2551640的基因型频率也无显著差异(p>0.05)。BDNF基因中的三个位点和CREB基因中的两个位点处于强连锁不平衡状态。与对照组相比,由BDNF基因中的三个位点组成的单倍型AAC(rs11030101/rs2030324/rs626)在精神分裂症患者中的频率显著增加。BDNF基因不同rs11030101基因型的患者,PANSS阴性症状子量表得分存在显著差异(p<0.05)。CREB基因不同rs6265基因型的患者,PANSS一般症状G12(判断力和自知力缺乏)得分也存在显著差异(p<0.05)。BDNF基因rs11030101/rs2030324/rs6265 AAC单倍型可能与精神分裂症风险增加有关。此外,rs11030101和rs6265位点的基因型可能分别影响精神分裂症患者的阴性症状和一般症状。

相似文献

引用本文的文献

本文引用的文献

6
Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.精神分裂症遗传学:WFSBP 遗传学工作组的共识文件。
World J Biol Psychiatry. 2017 Oct;18(7):492-505. doi: 10.1080/15622975.2016.1268715. Epub 2017 Jan 23.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验