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精神分裂症易感基因神经调节蛋白1的作用跨越传统诊断界限,增加双相情感障碍的患病风险。

Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder.

作者信息

Green Elaine K, Raybould Rachel, Macgregor Stuart, Gordon-Smith Katherine, Heron Jess, Hyde Sally, Grozeva Detelina, Hamshere Marian, Williams Nigel, Owen Michael J, O'Donovan Michael C, Jones Lisa, Jones Ian, Kirov George, Craddock Nick

机构信息

Department of Psychological Medicine and Biostatics and Bioinformatics Unit, University of Wales College of Medicine, Cardiff.

出版信息

Arch Gen Psychiatry. 2005 Jun;62(6):642-8. doi: 10.1001/archpsyc.62.6.642.

Abstract

CONTEXT

Family and twin data suggest that, in addition to susceptibility genes specific for bipolar disorder or schizophrenia, genes exist that contribute to susceptibility across the traditional kraepelinian divide. Several studies have provided evidence that variation at the neuregulin 1 (NRG1) gene on chromosome 8p12 influences susceptibility to schizophrenia. The most consistent finding has been that one particular haplotype (the "core" haplotype) is overrepresented in cases compared with control subjects.

OBJECTIVE

To investigate the possible role of NRG1 in bipolar disorder.

DESIGN

Genetic case-control association analysis.

SETTING

Subjects were unrelated and ascertained from general psychiatric inpatient and outpatient services.

PARTICIPANTS

Five hundred twenty-nine patients with DSM-IV bipolar I disorder and 1011 controls from the United Kingdom (100% white).

METHODS

We genotyped the markers constituting the NRG1 core haplotype in cases and controls and reanalyzed our existing data from 573 DSM-IV schizophrenia cases with this larger set of controls.

RESULTS

We found a significant difference in haplotype distribution between bipolar cases and controls globally (P = .003) and specifically for the core haplotype. Frequencies were 10.2% for bipolar cases and 7.8% for controls (effect size, as measured by odds ratio [OR], 1.37; 95% confidence interval [CI], 1.03-1.80; P = .04). The effect size in our bipolar sample was similar to that in our schizophrenia sample (OR, 1.22; 95% CI, 0.92-1.61). In the bipolar cases with predominantly mood-incongruent psychotic features (n = 193), the effect was greater (OR, 1.71; 95% CI, 1.29-2.59; P = .009), as was the case in the subset of schizophrenia cases (n = 27) who had experienced mania (OR, 1.64; 95% CI, 0.54-5.01).

CONCLUSIONS

Our findings suggest that neuregulin 1 plays a role in influencing susceptibility to bipolar disorder and schizophrenia and that it may exert a specific effect in the subset of functional psychosis that has manic and mood-incongruent psychotic features.

摘要

背景

家族和双生子数据表明,除了双相情感障碍或精神分裂症的特异性易感基因外,还存在一些基因,它们导致跨越传统克雷佩林分类界限的易感性。多项研究已提供证据表明,位于8号染色体p12区域的神经调节蛋白1(NRG1)基因变异会影响精神分裂症易感性。最一致的发现是,与对照受试者相比,一种特定的单倍型(“核心”单倍型)在病例中过度出现。

目的

研究NRG1在双相情感障碍中的可能作用。

设计

基因病例对照关联分析。

地点

受试者无亲缘关系,来自普通精神科住院和门诊服务机构。

参与者

529例符合DSM-IV标准的双相I型障碍患者和1011名来自英国的对照者(100%为白人)。

方法

我们对构成NRG1核心单倍型的标记物在病例组和对照组中进行基因分型,并使用这一更大的对照组重新分析我们现有的来自573例DSM-IV精神分裂症病例的数据。

结果

我们发现双相情感障碍病例组和对照组之间的单倍型分布存在显著差异(整体P = 0.003),特别是对于核心单倍型。双相情感障碍病例组的频率为10.2%,对照组为7.8%(效应量,以优势比[OR]衡量,为1.37;95%置信区间[CI],1.03 - 1.80;P = 0.04)。我们双相情感障碍样本中的效应量与精神分裂症样本中的相似(OR,1.22;95% CI,0.92 - 1.61)。在主要具有心境不和谐精神病性特征的双相情感障碍病例(n = 193)中,效应更大(OR,1.71;95% CI,1.29 - 2.59;P = 0.009),在经历过躁狂发作的精神分裂症病例子集(n = 27)中也是如此(OR,1.64;95% CI,0.54 - 5.01)。

结论

我们的研究结果表明,神经调节蛋白1在影响双相情感障碍和精神分裂症易感性方面发挥作用,并且它可能在具有躁狂和心境不和谐精神病性特征的功能性精神病子集中发挥特定作用。

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