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精神分裂症中海马体积的 G×E 交互作用的探索性模型;产科并发症和与缺氧相关的基因。

An exploratory model for G x E interaction on hippocampal volume in schizophrenia; obstetric complications and hypoxia-related genes.

机构信息

Department of Clinical Medicine, section Vinderen, University of Oslo, Norway.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2010 Oct 1;34(7):1259-65. doi: 10.1016/j.pnpbp.2010.07.001. Epub 2010 Jul 16.

Abstract

BACKGROUND

Smaller hippocampal volume has repeatedly been reported in schizophrenia patients. Obstetric complications (OCs) and single nucleotide polymorphism (SNP) variation in schizophrenia susceptibility genes have independently been related to hippocampal volume. We investigated putative independent and interaction effects of severe hypoxia-related OCs and variation in four hypoxia-regulated schizophrenia susceptibility genes (BDNF, DTNBP1, GRM3 and NRG1) on hippocampal volume in schizophrenia patients and healthy controls.

METHODS

Clinical assessment, structural MRI scans, and blood samples for genotyping of 32 SNPs were obtained from 54 schizophrenia patients and 53 control subjects. Information on obstetric complications was collected from original birth records.

RESULTS

Severe OCs were related to hippocampal volume in both patients with schizophrenia and healthy control subjects. Of the 32 SNPs studied, effects of severe OCs on hippocampal volume were associated with allele variation in GRM3 rs13242038, but the interaction effect was not specific for schizophrenia. SNP variation in any of the four investigated genes alone did not significantly affect hippocampal volume.

CONCLUSIONS

The findings suggest a gene-environment (G x E) interaction between GRM3 gene variants and severe obstetric complications on hippocampus volume, independent of a diagnosis of schizophrenia. Due to the modest sample size, the results must be considered preliminary and require replication in independent samples.

摘要

背景

精神分裂症患者的海马体体积较小已被反复报道。产科并发症(OCs)和精神分裂症易感基因中的单核苷酸多态性(SNP)变异独立地与海马体体积有关。我们研究了严重缺氧相关 OCs 和四个缺氧调节精神分裂症易感基因(BDNF、DTNBP1、GRM3 和 NRG1)中的变异在精神分裂症患者和健康对照者的海马体体积中可能存在的独立和交互作用。

方法

从 54 名精神分裂症患者和 53 名对照受试者中获得了临床评估、结构 MRI 扫描和用于 32 个 SNP 基因分型的血液样本。从原始出生记录中收集了产科并发症的信息。

结果

严重的 OCs 与精神分裂症患者和健康对照者的海马体体积有关。在研究的 32 个 SNP 中,严重 OCs 对海马体体积的影响与 GRM3 rs13242038 的等位基因变异有关,但这种相互作用并非特定于精神分裂症。单独研究的四个基因中的任何一个基因的 SNP 变异都不会显著影响海马体体积。

结论

这些发现表明,GRM3 基因变异与严重产科并发症之间存在基因-环境(G x E)相互作用,与精神分裂症的诊断无关。由于样本量较小,结果必须被认为是初步的,并需要在独立样本中进行复制。

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