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首页> 外文期刊>Human Molecular Genetics >Meta-analysis shows strong positive association of the neuregulin 1 (NRG1) gene with schizophrenia.
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Meta-analysis shows strong positive association of the neuregulin 1 (NRG1) gene with schizophrenia.

机译:荟萃分析显示神经调节蛋白1(NRG1)基因与精神分裂症有很强的正相关性。

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Chromosome 8p22-p11 has been identified as a locus for schizophrenia in several genome-wide scans and confirmed by meta-analysis of published linkage data. Systematic fine mapping using extended Icelandic pedigrees identified an associated haplotype in the gene neuregulin 1 (NRG1), also known as heuregulin, glial growth factor, NDF43 and ARIA. A 290 kb core at risk haplotype at the 5' end of the gene (HAP(ICE)), defined by five SNPs and two microsatellite polymorphisms was found to be associated with schizophrenia in the Icelandic and Scottish populations. A number of subsequent independent studies have attempted to replicate the association, and while some have been successful, the associated haplotype is not always HAP(ICE). Furthermore, no obviously functional or pathogenic variants have been identified, and the relationship between the gene and schizophrenia has remained inconclusive. To reconcile these conflicting findings and to give a comprehensive picture of the genetic architecture of this important gene, we performed a meta-analysis of 13 published population-based and family-based association studies up to November 2005. We analysed data from the SNP markers SNP8NRG241930, SNP8NRG243177, SNP8NRG221132 and SNP8NRG221533, and the microsatellite markers 478B14-848, 420M9-1395. Across these studies, strong positive association was found for all six polymorphisms. The haplotype analysis also showed significant association in the pooled international populations (OR=1.22, 95% CI 1.15-1.3, P=8 x 10(-10)). In Asian populations, the risk haplotype was focused around the two microsatellite markers, 478B14-848, 420M9-1395 (haplotype block B), and in Caucasian populations with the remaining four SNP markers (haplotype block A). This meta-analysis supports the involvement of NRG1 in the pathogenesis of schizophrenia, but with association between two different but adjacent haplotypes blocks in the Caucasian and Asian populations.
机译:在几次全基因组扫描中,染色体8p22-p11已被确定为精神分裂症的病灶,并通过已发表的连锁数据的荟萃分析得到证实。使用扩展的冰岛谱系进行系统精细定位,在神经调节蛋白1(NRG1)基因(也称为heuregulin,神经胶质生长因子,NDF43和ARIA)中鉴定了一个相关的单倍型。在冰岛和苏格兰人群中,由五个SNP和两个微卫星多态性定义的基因(HAP(ICE))5'端有一个290 kb的核心危险单倍型与精神分裂症有关。随后的许多独立研究都试图复制这种关联,尽管有些成功,但关联的单倍型并不总是HAP(ICE)。此外,尚未鉴定出明显的功能或致病性变体,并且该基因与精神分裂症之间的关系仍然不确定。为了调和这些矛盾的发现并全面了解该重要基因的遗传结构,我们对截至2005年11月的13项基于人群和基于家庭的关联研究进行了荟萃分析。我们分析了SNP标记数据SNP8NRG241930,SNP8NRG243177,SNP8NRG221132和SNP8NRG221533,以及微卫星标记478B14-848、420M9-1395。在这些研究中,发现所有六个多态性均具有强正相关。单倍型分析还显示在国际人群中有显着的相关性(OR = 1.22,95%CI 1.15-1.3,P = 8 x 10(-10))。在亚洲人群中,危险单倍型集中在两个微卫星标记478B14-848、420M9-1395(单倍型块B)上,在白种人人群中,其余四个SNP标记(单倍型块A)上。这项荟萃分析支持NRG1参与精神分裂症的发病机理,但与白种人和亚洲人群中两个不同但相邻的单倍型模块之间存在关联。

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