Suppr超能文献

OLIG2 基因座 rs1059004 多态性与首发精神分裂症全脑功能连接的关联。

Association of rs1059004 polymorphism in the OLIG2 locus with whole-brain functional connectivity in first-episode schizophrenia.

机构信息

School of Life Sciences and Technology, Xidian University, Xi'an, Shaanxi, 710071, PR China.

School of Life Sciences and Technology, Xidian University, Xi'an, Shaanxi, 710071, PR China.

出版信息

Behav Brain Res. 2020 Feb 3;379:112392. doi: 10.1016/j.bbr.2019.112392. Epub 2019 Nov 27.

Abstract

The rs1059004 in the oligodendrocyte lineage transcription factor 2 (OLIG2) gene has been reported to be a candidate single nucleotide polymorphism (SNP) for schizophrenia (SZ). A variety of functional magnetic resonance imaging (fMRI) studies have revealed disconnection in SZ. We aimed to investigate the association of rs1059004 polymorphism with whole-brain functional connectivity (FC) and to further explore the correlation between altered FC and cognitive behavioral scales. Fifty-five SZ patients and fifty-three matched healthy controls were included in this study. The general linear model was used to test the role of rs1059004 polymorphism in whole-brain FC based on resting-state fMRI. Spearman's rank correlation test was used to calculate the correlation coefficient between FC strength and behavior score. In the whole-brain FC analysis, we found that the FC pattern in SZ patients differs from healthy controls. Furthermore, compared to homozygous C carriers, risk A allele carriers have reduced FC strength in both SZ patients and healthy controls. For the correlation analysis in risk A allele carriers, we found a positive correlation between FC strength and verbal fluency score in SZ patients, while healthy controls appeared to have the opposite result. Our results revealed that participants carrying the risk A allele show FC patterns differing from those of homozygous C carriers. This result suggests that rs1059004 polymorphism and SZ have synergistic effects on brain connections. The correlation analysis result suggests that special attention should be paid to SZ patients who carry the risk A allele because the patients perform worse in verbal fluency.

摘要

rs1059004 位于少突胶质细胞系转录因子 2(OLIG2)基因中,被报道是精神分裂症(SZ)的候选单核苷酸多态性(SNP)。各种功能磁共振成像(fMRI)研究揭示了 SZ 中的连接中断。我们旨在研究 rs1059004 多态性与全脑功能连接(FC)的关联,并进一步探讨改变的 FC 与认知行为量表之间的相关性。本研究纳入了 55 名 SZ 患者和 53 名匹配的健康对照者。基于静息态 fMRI,我们使用一般线性模型来检验 rs1059004 多态性在全脑 FC 中的作用。使用 Spearman 秩相关检验计算 FC 强度与行为评分之间的相关系数。在全脑 FC 分析中,我们发现 SZ 患者的 FC 模式与健康对照组不同。此外,与纯合 C 携带者相比,风险 A 等位基因携带者在 SZ 患者和健康对照组中均表现出 FC 强度降低。对于风险 A 等位基因携带者的相关性分析,我们发现 SZ 患者的 FC 强度与言语流畅性评分呈正相关,而健康对照组似乎存在相反的结果。我们的结果表明,携带风险 A 等位基因的参与者表现出与纯合 C 携带者不同的 FC 模式。这一结果表明,rs1059004 多态性和 SZ 对大脑连接有协同作用。相关性分析结果表明,应特别关注携带风险 A 等位基因的 SZ 患者,因为这些患者在言语流畅性方面表现较差。

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