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精神分裂症和精神分裂症定量指标的遗传关联研究:多基因风险评分分析。

Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis.

机构信息

Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, The Netherlands.

出版信息

PLoS One. 2012;7(6):e37852. doi: 10.1371/journal.pone.0037852. Epub 2012 Jun 22.

Abstract

The presence of subclinical levels of psychosis in the general population may imply that schizophrenia is the extreme expression of more or less continuously distributed traits in the population. In a previous study, we identified five quantitative measures of schizophrenia (positive, negative, disorganisation, mania, and depression scores). The aim of this study is to examine the association between a direct measure of genetic risk of schizophrenia and the five quantitative measures of psychosis. Estimates of the log of the odds ratios of case/control allelic association tests were obtained from the Psychiatric GWAS Consortium (PGC) (minus our sample) which included genome-wide genotype data of 8,690 schizophrenia cases and 11,831 controls. These data were used to calculate genetic risk scores in 314 schizophrenia cases and 148 controls from the Netherlands for whom genotype data and quantitative symptom scores were available. The genetic risk score of schizophrenia was significantly associated with case-control status (p<0.0001). In the case-control sample, the five psychosis dimensions were found to be significantly associated with genetic risk scores; the correlations ranged between.15 and.27 (all p<.001). However, these correlations were not significant in schizophrenia cases or controls separately. While this study confirms the presence of a genetic risk for schizophrenia as categorical diagnostic trait, we did not find evidence for the genetic risk underlying quantitative schizophrenia symptom dimensions. This does not necessarily imply that a genetic basis is nonexistent, but does suggest that it is distinct from the polygenic risk score for schizophrenia.

摘要

一般人群中亚临床水平的精神病的存在可能意味着精神分裂症是人群中或多或少连续分布特征的极端表现。在之前的一项研究中,我们确定了五种精神分裂症的定量测量方法(阳性、阴性、紊乱、躁狂和抑郁评分)。本研究的目的是检验精神分裂症遗传风险的直接测量与五种定量精神病测量之间的关联。从包括 8690 例精神分裂症病例和 11831 例对照的全基因组基因型数据的精神疾病 GWAS 联盟(PGC)(减去我们的样本)获得病例/对照等位基因关联测试对数比值的估计值,并将这些数据用于计算荷兰的 314 例精神分裂症病例和 148 例对照的遗传风险评分,这些对照有基因型数据和定量症状评分。精神分裂症的遗传风险评分与病例对照状态显著相关(p<0.0001)。在病例对照样本中,发现五个精神病维度与遗传风险评分显著相关;相关系数在.15 到.27 之间(均 p<.001)。然而,这些相关性在精神分裂症病例或对照中均不显著。虽然这项研究证实了精神分裂症作为分类诊断特征存在遗传风险,但我们没有发现精神分裂症定量症状维度的遗传风险的证据。这并不一定意味着遗传基础不存在,但确实表明它与精神分裂症的多基因风险评分不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd76/3382234/660c4d878eb3/pone.0037852.g001.jpg

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