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NOTCH4 基因的常见变体调节枕叶皮层的功能连接及其与精神分裂特质的关系。

A common variant of the NOTCH4 gene modulates functional connectivity of the occipital cortex and its relationship with schizotypal traits.

机构信息

Department of Neurology, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, China.

Collaborative Innovation Center for Neuropsychiatric Disorders and Mental Health, Anhui Medical University, Hefei, 230022, China.

出版信息

BMC Psychiatry. 2020 Jul 9;20(1):363. doi: 10.1186/s12888-020-02773-z.

Abstract

BACKGROUND

Schizotypal traits are considered as inheritable traits and the endophenotype for schizophrenia. A common variant in the NOTCH4 gene, rs204993, has been linked with schizophrenia, but the neural underpinnings are largely unknown.

METHODS

In present study, we compared the differences of brain functions between different genotypes of rs204993 and its relationship with schizotypal traits among 402 Chinese Han healthy volunteers. The brain function was evaluated with functional connectivity strength (FCS) using the resting-state functional magnetic resonance image(rs-fMRI). The schizotypal traits were measured by the schizotypal personality questionnaire (SPQ).

RESULTS

Our results showed that carriers with the AA genotype showed reduced FCS in the left occipital cortex when compared with carriers with the AG and GG genotypes, and the carriers with the AG genotype showed reduced FCS in the left occipital cortex when compared with carriers with the GG genotype. The FCS values in the left occipital lobe were negatively associated with the SPQ scores and its subscale scores within the carriers with the GG genotype, but not within the carriers with AA or AG genotype.

CONCLUSION

Our results suggested that the common variant in the NOTCH4 gene, rs204993, modulates the function of the occipital cortex, which may contribute to schizotypal traits. These findings provide insight for genetic effects on schizotypal traits and its potential neural substrate.

摘要

背景

分裂型特质被认为是可遗传的特质,也是精神分裂症的内表型。NOTCH4 基因的一个常见变异体 rs204993 与精神分裂症有关,但神经基础在很大程度上尚不清楚。

方法

在本研究中,我们比较了不同 rs204993 基因型个体之间的脑功能差异及其与 402 名中国汉族健康志愿者的分裂型特质之间的关系。使用静息态功能磁共振成像(rs-fMRI)评估脑功能。使用分裂型人格问卷(SPQ)测量分裂型特质。

结果

我们的结果表明,与 AG 和 GG 基因型携带者相比,AA 基因型携带者的左侧枕叶皮质的功能连接强度(FCS)降低,而 AG 基因型携带者的左侧枕叶皮质的 FCS 降低与 GG 基因型携带者相比。在 GG 基因型携带者中,左侧枕叶的 FCS 值与 SPQ 评分及其亚量表评分呈负相关,但在 AA 或 AG 基因型携带者中则没有相关性。

结论

我们的研究结果表明,NOTCH4 基因的常见变异体 rs204993 调节了枕叶皮质的功能,这可能与分裂型特质有关。这些发现为遗传对分裂型特质及其潜在神经基础的影响提供了新的见解。

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