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Allergy and glioma risk: test of association by genotype.

机译:过敏和神经胶质瘤风险:按基因型进行的关联性测试。

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摘要

Although epidemiological studies have suggested an association between atopy and glioma risk, these observations have been based on self-reporting of allergic conditions raising the possibility that associations may be noncausal and arise as a consequence of bias, reverse causation or other artifacts. Genetic information provides an alternative approach to investigate the relationship avoiding such biases. We analyzed 1,878 glioma cases and 3,670 controls for variants at 2q12, 5q12.1, 11q13 and 17q21 that are associated with asthma or eczema risk at p < 5.0 x 10(-7) . The SNP rs7216389, which tags the 3' flanking region of ORMDL3 at 17q21 and has been associated with childhood asthma, was correlated with increased glioma risk (OR = 1.10; 95% CI: 1.01-1.19). These data provide evidence for a correlation between asthma susceptibility and glioma risk and illustrate the value of using genetics as an investigative tool for developing etiological hypotheses.
机译:尽管流行病学研究表明特应性疾病和神经胶质瘤风险之间存在关联,但这些观察是基于过敏性疾病的自我报告,从而增加了关联可能是无因果的,并且可能是由于偏见,反向因果关系或其他伪像而产生的。遗传信息为避免这种偏见提供了一种替代方法来研究这种关系。我们分析了1878例神经胶质瘤病例和3670例对照,分析了2q12、5q12.1、11q13和17q21时与p≤5.0 x 10(-7)的哮喘或湿疹风险有关的变异。 SNP rs7216389标记了17q21时ORMDL3的3'侧翼区域,并与儿童哮喘相关,与神经胶质瘤风险增加相关(OR = 1.10; 95%CI:1.01-1.19)。这些数据为哮喘易感性与神经胶质瘤风险之间的相关性提供了证据,并说明了使用遗传学作为发展病因假说的研究工具的价值。

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