Single-nucleotide polymorphisms of allergy-related genes and risk of adult glioma

被引:0
|
作者
Danielle M. Backes
Afshan Siddiq
David G. Cox
Federico C. F. Calboli
J. Michael Gaziano
Jing Ma
Meir Stampfer
David J. Hunter
Carlos A. Camargo
Dominique S. Michaud
机构
[1] Brown Public Health,Department of Epidemiology
[2] Brown University,School of Public Health, Faculty of Medicine
[3] Imperial College London,Lyon Cancer Research Center
[4] INSERM U1052/CNRS UMR 5286/UCBL1,Division of Preventive Medicine
[5] Brigham and Women’s Hospital,Channing Division of Network Medicine, Department of Medicine
[6] Brigham and Women’s Hospital and Harvard Medical School,Department of Epidemiology
[7] Harvard School of Public Health,Department of Nutrition
[8] Harvard School of Public Health,Department of Emergency Medicine
[9] Massachusetts General Hospital,undefined
来源
Journal of Neuro-Oncology | 2013年 / 113卷
关键词
Brain tumors; Glioma; Allergies; Single-nucleotide polymorphisms; Cohort studies;
D O I
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中图分类号
学科分类号
摘要
Previous studies have shown an inverse association between allergies and glioma risk; however, results for associations between single nucleotide polymorphisms (SNPs) of allergy-related genes and glioma risk have been inconsistent and restricted to a small number of SNPs. The objective of this study was to examine the association between 166 SNPs of 21 allergy-related genes and glioma risk in a nested case–control study of participants from three large US prospective cohort studies. Blood collection took place between 1982 and 1994 among the 562 included Caucasian participants (143 cases and 419 matched controls) prior to case diagnosis. Custom Illumina assay chips were used for genotyping. Logistic regression analyses, controlling for age and study cohort, were used to determine associations between each SNP and glioma risk. Statistically significant associations were found between rs2494262 and rs2427824 of the FCER1A gene, which encodes the alpha chain of the high affinity immunoglobulin E receptor, and glioma risk (nominal trend p values 0.01 and 0.03, respectively). Significant associations were also found between SNPs in IL10, ADAM33, NOS1 and IL4R and glioma risk. However, our analyses were not corrected for multiple comparisons and need to be interpreted with caution. Our findings with FCER1A SNPs provide further support for the link between allergies and risk of glioma.
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页码:229 / 238
页数:9
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