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本文引用的文献

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Exposure to benzene and childhood leukaemia: a pilot case-control study.苯暴露与儿童白血病:一项初步的病例对照研究。
BMJ Open. 2013 Feb 26;3(2). doi: 10.1136/bmjopen-2012-002275. Print 2013.
2
Case-control study of paternal occupation and childhood leukaemia in Great Britain, 1962-2006.英国 1962-2006 年父亲职业与儿童白血病的病例对照研究。
Br J Cancer. 2012 Oct 23;107(9):1652-9. doi: 10.1038/bjc.2012.359. Epub 2012 Sep 11.
3
A record-based case-control study of natural background radiation and the incidence of childhood leukaemia and other cancers in Great Britain during 1980-2006.基于记录的病例对照研究:1980-2006 年英国自然本底辐射与儿童白血病和其他癌症发病的关系。
Leukemia. 2013 Jan;27(1):3-9. doi: 10.1038/leu.2012.151. Epub 2012 Jun 5.
4
Folic acid supplementation, MTHFR and MTRR polymorphisms, and the risk of childhood leukemia: the ESCALE study (SFCE).叶酸补充、MTHFR 和 MTRR 多态性与儿童白血病风险:ESCALE 研究(SFCE)。
Cancer Causes Control. 2012 Aug;23(8):1265-77. doi: 10.1007/s10552-012-0004-0. Epub 2012 Jun 16.
5
Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE).基因多态性与儿童急性淋巴细胞白血病:ESCALE研究(SFCE)的全基因组关联研究
Leukemia. 2012 Dec;26(12):2561-4. doi: 10.1038/leu.2012.148. Epub 2012 Jun 4.
6
Common variation in genes related to immune response and risk of childhood leukemia.与免疫反应和儿童期白血病风险相关的基因中的常见变异。
Hum Immunol. 2012 Mar;73(3):316-9. doi: 10.1016/j.humimm.2011.12.018. Epub 2011 Dec 28.
7
Association between Ataxia Telangiectasia Mutated gene polymorphisms and childhood leukemia in Taiwan.台湾地区共济失调毛细血管扩张症突变基因多态性与儿童白血病之间的关联。
Chin J Physiol. 2011 Dec 31;54(6):413-8. doi: 10.4077/CJP.2011.AMM106.
8
Maternal smoking during pregnancy, genetic polymorphisms of metabolic enzymes, and childhood acute leukemia: the ESCALE study (SFCE).孕期母亲吸烟、代谢酶遗传多态性与儿童急性白血病:ESCALE 研究(SFCE)。
Cancer Causes Control. 2012 Feb;23(2):329-45. doi: 10.1007/s10552-011-9882-9. Epub 2011 Dec 27.
9
Parental prenatal smoking and risk of childhood acute lymphoblastic leukemia.父母孕期吸烟与儿童急性淋巴细胞白血病风险。
Am J Epidemiol. 2012 Jan 1;175(1):43-53. doi: 10.1093/aje/kwr275. Epub 2011 Dec 5.
10
Family history of cancer and non-malignant diseases and risk of childhood acute lymphoblastic leukemia: a Children's Oncology Group Study.癌症和非恶性疾病家族史与儿童急性淋巴细胞白血病风险:儿童肿瘤协作组研究。
Cancer Epidemiol. 2012 Feb;36(1):45-51. doi: 10.1016/j.canep.2011.06.004. Epub 2011 Oct 21.

儿童白血病国际联合会。

The Childhood Leukemia International Consortium.

机构信息

University of California, Berkeley, School of Public Health, 1995 University Avenue, Suite 460, Berkeley, CA 94704-1070, USA.

出版信息

Cancer Epidemiol. 2013 Jun;37(3):336-47. doi: 10.1016/j.canep.2012.12.011. Epub 2013 Feb 9.

DOI:10.1016/j.canep.2012.12.011
PMID:23403126
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3652629/
Abstract

BACKGROUND

Acute leukemia is the most common cancer in children under 15 years of age; 80% are acute lymphoblastic leukemia (ALL) and 17% are acute myeloid leukemia (AML). Childhood leukemia shows further diversity based on cytogenetic and molecular characteristics, which may relate to distinct etiologies. Case-control studies conducted worldwide, particularly of ALL, have collected a wealth of data on potential risk factors and in some studies, biospecimens. There is growing evidence for the role of infectious/immunologic factors, fetal growth, and several environmental factors in the etiology of childhood ALL. The risk of childhood leukemia, like other complex diseases, is likely to be influenced both by independent and interactive effects of genes and environmental exposures. While some studies have analyzed the role of genetic variants, few have been sufficiently powered to investigate gene-environment interactions.

OBJECTIVES

The Childhood Leukemia International Consortium (CLIC) was established in 2007 to promote investigations of rarer exposures, gene-environment interactions and subtype-specific associations through the pooling of data from independent studies.

METHODS

By September 2012, CLIC included 22 studies (recruitment period: 1962-present) from 12 countries, totaling approximately 31000 cases and 50000 controls. Of these, 19 case-control studies have collected detailed epidemiologic data, and DNA samples have been collected from children and child-parent trios in 15 and 13 of these studies, respectively. Two registry-based studies and one study comprising hospital records routinely obtained at birth and/or diagnosis have limited interview data or biospecimens.

CONCLUSIONS

CLIC provides a unique opportunity to fill gaps in knowledge about the role of environmental and genetic risk factors, critical windows of exposure, the effects of gene-environment interactions and associations among specific leukemia subtypes in different ethnic groups.

摘要

背景

急性白血病是 15 岁以下儿童中最常见的癌症;80%为急性淋巴细胞白血病(ALL),17%为急性髓细胞白血病(AML)。儿童白血病根据细胞遗传学和分子特征进一步多样化,这可能与不同的病因有关。全球开展的病例对照研究,特别是 ALL,收集了大量有关潜在危险因素的数据,在一些研究中还收集了生物标本。越来越多的证据表明,感染/免疫因素、胎儿生长和几种环境因素在儿童 ALL 的病因中起作用。与其他复杂疾病一样,儿童白血病的风险可能受到基因和环境暴露的独立和相互作用的影响。虽然一些研究分析了遗传变异的作用,但很少有研究有足够的能力来研究基因-环境相互作用。

目的

儿童白血病国际联盟(CLIC)成立于 2007 年,旨在通过汇集来自独立研究的数据,促进对罕见暴露、基因-环境相互作用和亚型特异性关联的研究。

方法

截至 2012 年 9 月,CLIC 包括来自 12 个国家的 22 项研究(招募期:1962 年至今),总计约 31000 例病例和 50000 例对照。其中,19 项病例对照研究收集了详细的流行病学数据,15 项研究收集了儿童的 DNA 样本,13 项研究收集了儿童及其父母三人间的 DNA 样本。两项基于登记的研究和一项包含出生时和/或诊断时常规获得的医院记录的研究只有有限的访谈数据或生物标本。

结论

CLIC 提供了一个独特的机会,可以填补有关环境和遗传危险因素、暴露关键期、基因-环境相互作用的影响以及不同种族群体中特定白血病亚型之间关联的知识空白。