Division of Epidemiology, School of Public Health, University of California, 1995 University Ave, Ste 460, Berkeley, CA, 94704, USA,
Cancer Causes Control. 2013 Oct;24(10):1789-95. doi: 10.1007/s10552-013-0256-3. Epub 2013 Jul 9.
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.
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。