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Genetic Screening of Plasticity Regulating Nogo-Type Signaling Genes in Migraine

机译:偏头痛可塑性调节Nogo型信号基因的遗传筛选。

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摘要

Migraine is the sixth most prevalent disease in the world and a substantial number of experiments have been conducted to analyze potential differences between the migraine brain and the healthy brain. Results from these investigations point to the possibility that development and aggravation of migraine may include grey matter plasticity. Nogo-type signaling is a potent plasticity regulating system in the CNS and consists of ligands, receptors, co-receptors and modulators with a dynamic age- and activity-related expression in cortical and subcortical regions. Here we investigated a potential link between migraine and five key Nogo-type signaling genes: , , , and by screening 15 single nucleotide polymorphisms (SNPs) within these genes. In a large Swedish migraine cohort (749 migraine patients and 4032 controls), using a logistic regression with sex as covariate, we found that there was no such association. In addition, a haplotype analysis was performed which revealed three haplotype blocks. These blocks had no significant association with migraine. However, to robustly conclude that Nogo-type genotypes signaling do not influence the prevalence of migraine, further studies are encouraged.
机译:偏头痛是世界上第六种最普遍的疾病,并且已经进行了大量的实验来分析偏头痛和健康大脑之间的潜在差异。这些调查的结果表明,偏头痛的发展和恶化可能包括灰质可塑性。 Nogo型信号传导是CNS中有效的可塑性调节系统,由配体,受体,共受体和调节剂组成,在皮质和皮质下区域具有与年龄和活动相关的动态表达。在这里,我们通过筛选15个单核苷酸多态性(SNPs)来研究偏头痛与五个关键Nogo型信号转导基因之间的潜在联系。在瑞典的大型偏头痛队列(749名偏头痛患者和4032名对照)中,使用性别作为协变量的逻辑回归,我们发现没有这种关联。另外,进行了单倍型分析,揭示了三个单倍型模块。这些阻滞与偏头痛无明显关联。但是,为了有力地得出结论,Nogo型基因型信号传导不会影响偏头痛的发生,鼓励进一步的研究。

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