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本文引用的文献

1
Independent evidence for the selective influence of GABA(A) receptors on one component of the bipolar disorder phenotype.γ-氨基丁酸A(GABA(A))受体对双相情感障碍表型的一个组成部分具有选择性影响的独立证据。
Mol Psychiatry. 2011 Jun;16(6):587-9. doi: 10.1038/mp.2010.67. Epub 2010 Jun 15.
2
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder.ZNF804A 的精细定位及全基因组范围内的证据表明其与精神分裂症和双相情感障碍有关。
Mol Psychiatry. 2011 Apr;16(4):429-41. doi: 10.1038/mp.2010.36. Epub 2010 Apr 6.
3
Severe mental disorders in offspring with 2 psychiatrically ill parents.父母双方均患有精神疾病的后代中的严重精神障碍
Arch Gen Psychiatry. 2010 Mar;67(3):252-7. doi: 10.1001/archgenpsychiatry.2010.1.
4
Dissecting the phenotype in genome-wide association studies of psychiatric illness.剖析精神疾病全基因组关联研究中的表型
Br J Psychiatry. 2009 Aug;195(2):97-9. doi: 10.1192/bjp.bp.108.063156.
5
The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia.CACNA1C 上的双相情感障碍风险等位基因也会增加复发性重度抑郁和精神分裂症的风险。
Mol Psychiatry. 2010 Oct;15(10):1016-22. doi: 10.1038/mp.2009.49. Epub 2009 Jul 21.
6
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.常见的多基因变异会增加患精神分裂症和双相情感障碍的风险。
Nature. 2009 Aug 6;460(7256):748-52. doi: 10.1038/nature08185. Epub 2009 Jul 1.
7
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept.广义双相分裂情感性障碍作为一种诊断概念的遗传学效用。
Br J Psychiatry. 2009 Jul;195(1):23-9. doi: 10.1192/bjp.bp.108.061424.
8
Genomewide association studies: history, rationale, and prospects for psychiatric disorders.全基因组关联研究:精神疾病的历史、原理及前景
Am J Psychiatry. 2009 May;166(5):540-56. doi: 10.1176/appi.ajp.2008.08091354. Epub 2009 Apr 1.
9
Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or "schizoaffective") psychoses.精神病遗传学:构建精神分裂症、双相情感障碍和混合型(或“分裂情感性”)精神病之间的关系模型。
Schizophr Bull. 2009 May;35(3):482-90. doi: 10.1093/schbul/sbp020. Epub 2009 Mar 27.
10
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study.瑞典家庭中精神分裂症和双相情感障碍的常见遗传决定因素:一项基于人群的研究。
Lancet. 2009 Jan 17;373(9659):234-9. doi: 10.1016/S0140-6736(09)60072-6.

双相情感障碍表型的多基因解析。

Polygenic dissection of the bipolar phenotype.

机构信息

MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK.

出版信息

Br J Psychiatry. 2011 Apr;198(4):284-8. doi: 10.1192/bjp.bp.110.087866.

DOI:10.1192/bjp.bp.110.087866
PMID:21972277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3065773/
Abstract

BACKGROUND

Recent data provide strong support for a substantial common polygenic contribution (i.e. many alleles each of small effect) to genetic susceptibility for schizophrenia and overlapping susceptibility for bipolar disorder.

AIMS

To test hypotheses about the relationship between schizophrenia and psychotic types of bipolar disorder.

METHOD

Using a polygenic score analysis to test whether schizophrenia polygenic risk alleles, en masse, significantly discriminate between individuals with bipolar disorder with and without psychotic features. The primary sample included 1829 participants with bipolar disorder and the replication sample comprised 506 people with bipolar disorder.

RESULTS

The subset of participants with Research Diagnostic Criteria schizoaffective bipolar disorder (n = 277) were significantly discriminated from the remaining participants with bipolar disorder (n = 1552) in both the primary (P = 0.00059) and the replication data-sets (P = 0.0070). In contrast, those with psychotic bipolar disorder as a whole were not significantly different from those with non-psychotic bipolar disorder in either data-set.

CONCLUSIONS

Genetic susceptibility influences at least two major domains of psychopathological variation in the schizophrenia-bipolar disorder clinical spectrum: one that relates to expression of a 'bipolar disorder-like' phenotype and one that is associated with expression of 'schizophrenia-like' psychotic symptoms.

摘要

背景

最近的数据为精神分裂症和双相情感障碍的遗传易感性具有大量共同的多基因贡献(即许多小效应的等位基因)提供了强有力的支持,并且存在重叠的易感性。

目的

检验关于精神分裂症和双相情感障碍精神病性类型之间关系的假设。

方法

使用多基因评分分析来测试精神分裂症多基因风险等位基因是否总体上显著区分具有和不具有精神病特征的双相情感障碍个体。主要样本包括 1829 名双相情感障碍患者,复制样本包括 506 名双相情感障碍患者。

结果

研究诊断标准为精神分裂症双相情感障碍的参与者子集(n = 277)在主要(P = 0.00059)和复制数据集(P = 0.0070)中与其余双相情感障碍患者(n = 1552)显著区分。相比之下,在这两个数据集中,整个精神病性双相情感障碍患者与非精神病性双相情感障碍患者之间没有显著差异。

结论

遗传易感性至少影响精神分裂症-双相情感障碍临床谱系中两个主要的精神病理学变异领域:一个与表现出“类似双相情感障碍”的表型有关,另一个与表现出“类似精神分裂症”的精神病性症状有关。