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Neuroblastoma in relation to joint effects of vitamin A and maternal and offspring variants in vitamin A-related genes: A report of the Children's Oncology Group

机译:神经母细胞瘤与维生素A和母体和后代变体在维生素A相关基因中的关节作用:儿童肿瘤学群的报告

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Background: There is evidence vitamin A plays a role in neuroblastoma. Not only is 13-czs-retinoic acid used as maintenance therapy for high-risk cases, but prenatal vitamin intake use may decrease neuroblastoma risk. We hypothesized that single nucleotide polymorphisms (SNPs) in vitamin A-related genes are may be associated with neuroblastoma risk and potentially be modified by vitamin A intake. Methods: The Neuroblastoma Epidemiology in North America (NENA) study recruited 563 case-parent sets through the Children's Oncology Group's Childhood Cancer Research Network. We ascertained dietary nutrient intake through questionnaires and genotyped 463 SNPs in vitamin A-related genes from saliva DNA. Offspring and maternal log-additive risk ratios (RR) and stratum-specific RR for gene-environment interaction were estimated with a log-linear model. We avoided false positives due to multiple testing by using the false discovery rate (FDR). Results: When all neuroblastoma cases were considered together, no offspring variants met the significance criteria (FDR Q-value < 0.2). One maternal SNP (rsl2442054) was associated with decreased risk of neuroblastoma (RR: 0.61; 95% Confidence Interval (CI): 0.47-0.79, Q = 0.076). When the cases were categorized according to prognostic risk category and age at onset, nine offspring SNPs were significantly associated with intermediate-risk neuroblastoma. Maternal rs6776706 was associated with (RR: 0.49; 95% CI: 0.33-0.72, Q = 0.161) high-risk neuroblastoma and maternal rs11103603 (RR: 0.60; 95% CI: 0.45-0.79, Q = 0.127) was associated with neuroblastoma aged < 1 year. For gene-environment interaction, maternal rs729147 was associated with decreased risk of neuroblastoma among mothers with vitamin A consumption above the recommendation. Conclusions: Although there is biologic plausibility for the role of vitamin A in neuroblastoma, we found weak evidence of a relationship between vitamin A related genes and neuroblastoma.
机译:背景:有证据是一种在神经母细胞瘤中发挥作用。不仅是13-CZS-视黄酸,用作高风险案例的维护疗法,但产前维生素的进气量可能会降低神经母细胞瘤风险。我们假设维生素A相关基因中的单一核苷酸多态性(SNP)可能与神经母细胞瘤风险有关,并且可能通过维生素A摄入来修饰。方法:北美神经母细胞瘤流行病学(NENA)研究通过儿童肿瘤学院的儿童癌症研究网络招聘了563例案件套。我们通过调查问卷和基因分型463 snps来确定膳食营养素摄入来自唾液DNA的维生素A相关基因。用LOG-LINEAR模型估计了对基因环境相互作用的后代和母体对数性风险比(RR)和特异性特异性RR。我们通过使用虚假发现速率(FDR)来避免由于多次测试而避免了误报。结果:当所有神经母细胞瘤病例中被认为是一起时,没有后代变体符合重要性标准(FDR Q值<0.2)。一种母体SNP(RSL2442054)与神经母细胞瘤的风险降低有关(RR:0.61; 95%置信区间(CI):0.47-0.79,Q = 0.076)。当根据预后风险类别和生病的年龄进行分类,九个后代SNP与中间风险神经母细胞瘤显着相关。母体RS6776706与(RR:0.49; 95%CI:0.33-0.72,Q = 0.161)高风险神经母细胞瘤和母体RS11103603(RR:0.60; 95%CI:0.45-0.79,Q = 0.127)与神经母细胞瘤有关年龄<1年。对于基因环境相互作用,母体RS729147与母亲在母中性母细胞瘤之间的风险降低有关,维生素是在推荐方面的消费。结论:虽然具有生物合理性的生物母细胞瘤中的作用,但我们发现维生素A相关基因和神经母细胞瘤之间关系的弱证据。

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