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Cross-disorder analysis of schizophrenia and 19 immune-mediated diseases identifies shared genetic risk

机译:精神分裂症和19种免疫介导的疾病的跨无序分析确定了共同的遗传风险

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摘要

Many immune diseases occur at different rates among people with schizophrenia compared to the general population. Here, we evaluated whether this phenomenon might be explained by shared genetic risk factors. We used data from large genome-wide association studies to compare the genetic architecture of schizophrenia to 19 immune diseases. First, we evaluated the association with schizophrenia of 581 variants previously reported to be associated with immune diseases at genome-wide significance. We identified five variants with potentially pleiotropic effects. While colocalization analyses were inconclusive, functional characterization of these variants provided the strongest evidence for a model in which genetic variation at rs1734907 modulates risk of schizophrenia and Crohn's disease via altered methylation and expression of EPHB4-a gene whose protein product guides the migration of neuronal axons in the brain and the migration of lymphocytes towards infected cells in the immune system. Next, we investigated genome-wide sharing of common variants between schizophrenia and immune diseases using cross-trait LD score regression. Of the 11 immune diseases with available genome-wide summary statistics, we observed genetic correlation between six immune diseases and schizophrenia: inflammatory bowel disease (r(g) = 0.12 +/- 0.03, P = 2.49 x 10(-4)), Crohn's disease (r(g) = 0.097 +/- 0.06, P = 3.27 x 10(-3)), ulcerative colitis (r(g) = 0.11 +/- 0.04, P = 4.05 x 10(-3)), primary biliary cirrhosis (r(g) = 0.13 +/- 0.05, P = 3.98 x 10(-3)), psoriasis (r(g) = 0.18 +/- 0.07, P = 7.78 x 10(-3)) and systemic lupus erythematosus (r(g) = 0.13 +/- 0.05, P = 3.76 x 10(-3)). With the exception of ulcerative colitis, the degree and direction of these genetic correlations were consistent with the expected phenotypic correlation based on epidemiological data. Our findings suggest shared genetic risk factors contribute to the epidemiological association of certain immune diseases and schizophrenia.
机译:与一般人群相比,许多免疫疾病在具有精神分裂症的人群中发生不同的速率。在这里,我们评估了这种现象是否可以通过共同的遗传危险因素来解释。我们使用来自大型基因组协会研究的数据,比较精神分裂症到19种免疫疾病的遗传建筑。首先,我们评估了先前据报道的581个变体的精神分裂症的关联,以在全基因组的意义上与免疫疾病相关。我们确定了五种具有潜在脂肪效应的变体。虽然分层分析是不确定的,但是这些变体的功能表征为一个模型提供了最强的证据,其中rs1734907的遗传变异调节精神分裂症和克罗恩病的风险,通过改变甲基化和ephb4-a蛋白质产品导向神经元轴突迁移的基因在大脑和淋巴细胞迁移到免疫系统中受感染细胞的迁移。接下来,我们使用交叉特征LD分数回归研究了精神分裂症和免疫疾病之间的常见变体的全基因组共享。在具有可用基因组概述统计的11个免疫疾病中,我们观察到六种免疫疾病和精神分裂症之间的遗传相关性:炎症性肠病(R(g)= 0.12 +/- 0.03,p = 2.49 x 10(-4)),克罗恩病(R(g)= 0.097 +/- 0.06,p = 3.27×10(-3)),溃疡性结肠炎(r(g)= 0.11 +/- 0.04,p = 4.05 x 10(-3)),原代胆汁肝硬化(R(g)= 0.13 +/- 0.05,p = 3.98×10(-3)),牛皮癣(R(g)= 0.18 +/- 0.07,p = 7.78 x 10(-3))和Systemic Lupus红斑(R(g)= 0.13 +/- 0.05,p = 3.76 x 10(-3))。除溃疡性结肠炎外,这些遗传相关的程度和方向与基于流行病学数据的预期表型相关性一致。我们的研究结果表明共享的遗传危险因素有助于某些免疫疾病和精神分裂症的流行病学协会。

著录项

  • 来源
    《Human Molecular Genetics》 |2019年第20期|共16页
  • 作者单位

    Ctr Addict &

    Mental Hlth Campbell Family Mental Hlth Res Inst Toronto ON M5T 1R8 Canada;

    Seoul Natl Univ Coll Med Dept Biomed Sci Seoul 110799 South Korea;

    Univ Queensland Inst Mol Biosci Brisbane Qld 4065 Australia;

    Stanford Univ Sch Med Dept Psychiat &

    Behav Sci Ctr Sleep Sci &

    Med Palo Alto CA 94305 USA;

    Stanford Univ Sch Med Dept Psychiat &

    Behav Sci Ctr Sleep Sci &

    Med Palo Alto CA 94305 USA;

    Kings Coll London Sch Basic &

    Med Biosci Fac Life Sci &

    Med London WC2R 2LS England;

    Kings Coll London Sch Basic &

    Med Biosci Fac Life Sci &

    Med London WC2R 2LS England;

    Kings Coll London Sch Basic &

    Med Biosci Fac Life Sci &

    Med London WC2R 2LS England;

    Kings Coll London Sch Basic &

    Med Biosci Fac Life Sci &

    Med London WC2R 2LS England;

    CSIC IPBLN Granada 18016 Spain;

    Univ Texas Hlth Sci Ctr Houston Houston TX 77030 USA;

    Wellcome Trust Sanger Inst Wellcome Trust Genome Campus Cambridge CB10 1SA England;

    CSIC IPBLN Granada 18016 Spain;

    Univ Colorado Sch Med Human Med Genet &

    Genom Program Aurora CO 80045 USA;

    Univ Colorado Sch Med Human Med Genet &

    Genom Program Aurora CO 80045 USA;

    Univ Colorado Sch Med Human Med Genet &

    Genom Program Aurora CO 80045 USA;

    Childrens Hosp Philadelphia Div Human Genet Ctr Appl Genom Philadelphia PA 19104 USA;

    McGill Univ Endocrine Genet Lab Dept Pediat Ctr Hlth Montreal PQ H4A 3J1 Canada;

    Brigham &

    Womens Hosp Dept Med 75 Francis St Boston MA 02115 USA;

    Univ Lancaster Lancaster Med Sch Lancaster LA1 4YW England;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学遗传学;
  • 关键词

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