Childhood cancer in children with congenital anomalies in Oklahoma, 1997 to 2009.

Amanda E. Janitz, B. Neas, Janis E Campbell, Anne E Pate, J. Stoner, S. Magzamen, J. Peck
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引用次数: 21

Abstract

BACKGROUND Data-linkage studies have reported an association between congenital anomalies and childhood cancer. However, few studies have focused on the differences in the effect of congenital anomalies on cancer as a function of attained age. We aimed to examine associations between anomalies and childhood cancer as a function of attained age among children born in Oklahoma. METHODS Data were obtained from the Oklahoma State Department of Health from 1997 to 2009 (n = 591,235). We linked Vital Statistics records for singleton deliveries to the Oklahoma Birth Defects Registry and the Oklahoma Central Cancer Registry using name and birth date. To assess the relation between anomalies and childhood cancer, we used Cox regression analysis allowing for a nonproportional hazards for anomalies as a function of age. RESULTS There were 23,368 (4.0%) children with anomalies and 531 (0.1%) children with cancer. When considering 3-year age intervals, we detected an increased hazard of any childhood cancer in children with anomalies compared with those without anomalies before 1 year of age (hazard ratio, 14.1; 95% confidence interval, 8.3-23.7) and at 3 years of age (hazard ratio, 2.3; 95% confidence interval, 1.6-3.2). The increased hazard declined with increasing time since birth, with the effect diminished by 6 years of age. CONCLUSION Our results were consistent with previous studies indicating an increased rate of childhood cancer among children with anomalies at younger ages. Furthermore, our study added a methodological refinement of assessing the effect of anomalies as a function of attained age. Birth Defects Research (Part A) 106:633-642, 2016. © 2016 Wiley Periodicals, Inc.
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1997年至2009年俄克拉何马州先天性畸形儿童患癌症的情况。
背景数据链接研究已经报道了先天性异常和儿童癌症之间的关联。然而,很少有研究关注先天性异常对癌症的影响随年龄的变化。我们的目的是研究在俄克拉何马州出生的儿童中,异常和儿童癌症之间的关系作为达到年龄的函数。方法数据来自1997 - 2009年俄克拉荷马州卫生部(n = 591,235)。我们使用姓名和出生日期将单胎分娩的生命统计记录与俄克拉何马州出生缺陷登记处和俄克拉何马州中央癌症登记处联系起来。为了评估异常与儿童癌症之间的关系,我们使用Cox回归分析,允许异常的非比例风险作为年龄的函数。结果异常患儿23368例(4.0%),癌变患儿531例(0.1%)。当考虑3年的年龄间隔时,我们发现在1岁之前,与没有异常的儿童相比,有异常的儿童患任何儿童癌症的风险都增加(风险比,14.1;95%可信区间,8.3-23.7)和3岁时(风险比,2.3;95%置信区间,1.6-3.2)。随着出生时间的增加,增加的危险性下降,6岁时影响减弱。结论:我们的研究结果与先前的研究一致,表明在年龄较小的异常儿童中儿童癌症发病率增加。此外,我们的研究增加了评估异常影响作为达到年龄的函数的方法改进。出生缺陷研究(A辑)(06):633-642,2016。©2016 Wiley期刊公司
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来源期刊
Birth defects research. Part A, Clinical and molecular teratology
Birth defects research. Part A, Clinical and molecular teratology 医药科学, 胎儿发育与产前诊断, 生殖系统/围生医学/新生儿
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1.86
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3 months
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Issue Information Cover Image Corrigendum for: Levels of folate receptor autoantibodies in maternal and cord blood and risk of neural tube defects in a Chinese population, 106:685–695 (10.1002/bdra.23517) Acardiac twin pregnancies part III: Model simulations. Diprosopus: Systematic review and report of two cases.
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