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Constitutional epimutation as a mechanism for cancer causality and heritability?作为癌症因果关系和遗传性的机制,宪法外遗传改变?
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2
Risk of cancer among children with birth defects: a novel approach.出生缺陷儿童患癌症的风险:一种新方法。
Birth Defects Res A Clin Mol Teratol. 2015 Apr;103(4):284-91. doi: 10.1002/bdra.23364. Epub 2015 Mar 24.
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Epigenetic remodeling in B-cell acute lymphoblastic leukemia occurs in two tracks and employs embryonic stem cell-like signatures.B细胞急性淋巴细胞白血病中的表观遗传重塑通过两条途径发生,并采用胚胎干细胞样特征。
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The prenatal origins of cancer.癌症的产前起源。
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Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics.遗传流行病学与非综合征型结构出生缺陷:从候选基因到表观遗传学。
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Deaths: leading causes for 2010.死亡:2010年的主要死因。
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Cancer risk in children and adolescents with birth defects: a population-based cohort study.儿童和青少年出生缺陷与癌症风险:基于人群的队列研究。
PLoS One. 2013 Jul 17;8(7):e69077. doi: 10.1371/journal.pone.0069077. Print 2013.
8
Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.印记疾病贝克威思-威德曼综合征及相关疾病的表观遗传和遗传改变。
J Hum Genet. 2013 Jul;58(7):402-9. doi: 10.1038/jhg.2013.51. Epub 2013 May 30.
9
Are children with birth defects at higher risk of childhood cancers?患有出生缺陷的儿童患儿童癌症的风险是否更高?
Am J Epidemiol. 2012 Jun 15;175(12):1217-24. doi: 10.1093/aje/kwr470. Epub 2012 Apr 24.
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Cancer in children with nonchromosomal birth defects.儿童非染色体出生缺陷相关癌症。
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1997年至2009年俄克拉荷马州先天性异常儿童中的儿童癌症。

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

作者信息

Janitz Amanda E, Neas Barbara R, Campbell Janis E, Pate Anne E, Stoner Julie A, Magzamen Sheryl L, Peck Jennifer D

机构信息

Department of Biostatistics and Epidemiology, College of Public Health, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.

School of Nursing and Allied Health Sciences, Southwestern Oklahoma State University, Weatherford, Oklahoma.

出版信息

Birth Defects Res A Clin Mol Teratol. 2016 Jul;106(7):633-42. doi: 10.1002/bdra.23494. Epub 2016 Mar 4.

DOI:10.1002/bdra.23494
PMID:26945683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4946965/
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.

摘要

背景

数据关联研究报告了先天性异常与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影响随年龄增长的差异。我们旨在研究俄克拉荷马州出生儿童中,先天性异常与儿童癌症之间随年龄增长的关联。

方法

数据来自1997年至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荷马州出生缺陷登记处和俄克拉荷马州中央癌症登记处相链接。为了评估先天性异常与儿童癌症之间的关系,我们使用Cox回归分析,该分析考虑了先天性异常随年龄变化的非比例风险。

结果

有23,368名(4.0%)儿童患有先天性异常,531名(0.1%)儿童患有癌症。当按3岁年龄间隔考虑时,我们发现先天性异常儿童在1岁前(风险比,14.1;95%置信区间,8.3 - 23.7)和3岁时(风险比,2.3;95%置信区间,1.6 - 3.2)患任何儿童癌症的风险高于无先天性异常的儿童。随着出生后时间的增加,风险增加的幅度下降,到6岁时影响减弱。

结论

我们的结果与先前的研究一致,表明年龄较小的先天性异常儿童患儿童癌症的几率增加。此外,我们的研究在评估先天性异常随年龄增长的影响方面增加了方法上的改进。《出生缺陷研究(A部分)》106:633 - 642,2016年。© 2016威利期刊公司。