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本文引用的文献

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Matching on Race and Ethnicity in Case-Control Studies as a Means of Control for Population Stratification.病例对照研究中按种族和民族进行匹配作为控制人群分层的一种方法。
Epidemiology (Sunnyvale). 2011 Sep 29;1:101. doi: 10.4172/2161-1165.1000101.
2
Variation in xenobiotic transport and metabolism genes, household chemical exposures, and risk of childhood acute lymphoblastic leukemia.外源性物质转运和代谢基因的变异、家庭化学暴露与儿童急性淋巴细胞白血病风险。
Cancer Causes Control. 2012 Aug;23(8):1367-75. doi: 10.1007/s10552-012-9947-4. Epub 2012 Jun 7.
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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.
4
ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment outcome of childhood acute lymphoblastic leukemia.ARID5B 基因多态性导致儿童急性淋巴细胞白血病的发病率和治疗结果存在种族差异。
J Clin Oncol. 2012 Mar 1;30(7):751-7. doi: 10.1200/JCO.2011.38.0345. Epub 2012 Jan 30.
5
Haplotypes of DNA repair and cell cycle control genes, X-ray exposure, and risk of childhood acute lymphoblastic leukemia.DNA 修复和细胞周期控制基因的单倍型、X 射线暴露与儿童急性淋巴细胞白血病风险。
Cancer Causes Control. 2011 Dec;22(12):1721-30. doi: 10.1007/s10552-011-9848-y. Epub 2011 Oct 11.
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Mapping genes that predict treatment outcome in admixed populations.在混合人群中定位预测治疗效果的基因。
Pharmacogenomics J. 2010 Dec;10(6):465-77. doi: 10.1038/tpj.2010.71. Epub 2010 Oct 5.
7
Variation at 7p12.2 and 10q21.2 influences childhood acute lymphoblastic leukemia risk in the Thai population and may contribute to racial differences in leukemia incidence.7p12.2 和 10q21.2 处的变异影响泰国人群儿童急性淋巴细胞白血病的发病风险,并且可能导致白血病发病率的种族差异。
Leuk Lymphoma. 2010 Oct;51(10):1870-4. doi: 10.3109/10428194.2010.511356.
8
Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia.复制分析证实了 ARID5B 与儿童 B 细胞急性淋巴细胞白血病的关联。
Haematologica. 2010 Sep;95(9):1608-11. doi: 10.3324/haematol.2010.022459. Epub 2010 May 11.
9
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.9p21.3 上的 CDKN2A 变异影响儿童急性淋巴细胞白血病的风险。
Nat Genet. 2010 Jun;42(6):492-4. doi: 10.1038/ng.585. Epub 2010 May 9.
10
ARID5B SNP rs10821936 is associated with risk of childhood acute lymphoblastic leukemia in blacks and contributes to racial differences in leukemia incidence.ARID5B基因单核苷酸多态性rs10821936与黑人儿童急性淋巴细胞白血病风险相关,并导致白血病发病率的种族差异。
Leukemia. 2010 Apr;24(4):894-6. doi: 10.1038/leu.2009.277. Epub 2010 Jan 7.

ARID5B 和 CEBPE 中的遗传变异是西班牙裔儿童 ALL 易感性的位点。

Genetic variants in ARID5B and CEBPE are childhood ALL susceptibility loci in Hispanics.

机构信息

Division of Epidemiology, School of Public Health, University of California, 1995 University Ave, Ste 460, Berkeley, CA, 94704, USA,

出版信息

Cancer Causes Control. 2013 Oct;24(10):1789-95. doi: 10.1007/s10552-013-0256-3. Epub 2013 Jul 9.

DOI:10.1007/s10552-013-0256-3
PMID:23836053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3771434/
Abstract

Recent genome-wide studies conducted in European Whites have identified novel susceptibility genes for childhood acute lymphoblastic leukemia (ALL). We sought to examine whether these loci are susceptibility genes among Hispanics, whose reported incidence of childhood ALL is the highest of all ethnic groups in California, and whether their effects differ between Hispanics and non-Hispanic Whites (NHWs). We genotyped 13 variants in these genes among 706 Hispanic (300 cases, 406 controls) and 594 NHW (225 cases, 369 controls) participants in a matched population-based case-control study in California. We found significant associations for the five studied ARID5B variants in both Hispanics (p values of 1.0 × 10(-9) to 0.004) and NHWs (p values of 2.2 × 10(-6) to 0.018). Risk estimates were in the same direction in both groups (ORs of 1.53-1.99 and 1.37-1.84, respectively) and strengthened when restricted to B-cell precursor high-hyperdiploid ALL (>50 chromosomes; ORs of 2.21-3.22 and 1.67-2.71, respectively). Similar results were observed for the single CEBPE variant. Hispanics and NHWs exhibited different susceptibility loci at CDKN2A. Although IKZF1 loci showed significant susceptibility effects among NHWs (p < 1 × 10(-5)), their effects among Hispanics were in the same direction but nonsignificant, despite similar minor allele frequencies. Future studies should examine whether the observed effects vary by environmental, immunological, or lifestyle factors.

摘要

最近在欧洲白人中进行的全基因组研究确定了儿童急性淋巴细胞白血病(ALL)的新的易感基因。我们试图研究这些基因座是否是西班牙裔人群中的易感基因,西班牙裔人群在加利福尼亚州所有种族群体中 ALL 的发病率最高,以及它们在西班牙裔和非西班牙裔白人(NHW)之间的作用是否不同。我们在加利福尼亚州的一项基于人群的匹配病例对照研究中,对 706 名西班牙裔(300 例病例,406 名对照)和 594 名 NHW(225 例病例,369 名对照)参与者中的 13 个这些基因中的变体进行了基因分型。我们发现,在西班牙裔人群(p 值范围为 1.0×10(-9) 至 0.004)和 NHW 人群(p 值范围为 2.2×10(-6) 至 0.018)中,这五个研究的 ARID5B 变体均存在显著关联。两组的风险估计值方向相同(OR 值分别为 1.53-1.99 和 1.37-1.84),当限制为 B 细胞前体高-超二倍体 ALL(>50 条染色体;OR 值分别为 2.21-3.22 和 1.67-2.71)时,风险估计值则更强。CEBPE 变体的单一变体也观察到了类似的结果。CDKN2A 处的西班牙裔和 NHW 表现出不同的易感基因座。尽管 IKZF1 基因座在 NHW 中表现出显著的易感作用(p < 1×10(-5)),但其在西班牙裔人群中的作用方向相同,但没有统计学意义,尽管其次要等位基因频率相似。未来的研究应检查观察到的影响是否因环境、免疫或生活方式因素而异。