Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia, WA, Australia, On behalf of the Aus-ALL Consortium (Australia).
Int J Cancer. 2013 Dec 15;133(12):2968-79. doi: 10.1002/ijc.28314. Epub 2013 Aug 1.
Positive associations have been reported between the measures of accelerated fetal growth and risk of childhood acute lymphoblastic leukemia (ALL). We investigated this association by pooling individual-level data from 12 case-control studies participating in the Childhood Leukemia International Consortium. Two measures of fetal growth-weight-for-gestational-age and proportion of optimal birth weight (POBW)-were analysed. Study-specific odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using multivariable logistic regression, and combined in fixed effects meta-analyses. Pooled analyses of all data were also undertaken using multivariable logistic regression. Subgroup analyses were undertaken when possible. Data on weight for gestational age were available for 7,348 cases and 12,489 controls from all 12 studies and POBW data were available for 1,680 cases and 3,139 controls from three studies. The summary ORs from the meta-analyses were 1.24 (95% CI: 1.13, 1.36) for children who were large for gestational age relative to appropriate for gestational age, and 1.16 (95% CI: 1.09, 1.24) for a one-standard deviation increase in POBW. The pooled analyses produced similar results. The summary and pooled ORs for small-for-gestational-age children were 0.83 (95% CI: 0.75, 0.92) and 0.86 (95% CI: 0.77, 0.95), respectively. Results were consistent across subgroups defined by sex, ethnicity and immunophenotype, and when the analysis was restricted to children who did not have high birth weight. The evidence that accelerated fetal growth is associated with a modest increased risk of childhood ALL is strong and consistent with known biological mechanisms involving insulin-like growth factors. © 2013 UICC.
已有研究表明,胎儿生长加速的各项指标与儿童期急性淋巴细胞白血病(ALL)的发病风险呈正相关。我们通过汇集参与儿童白血病国际联盟的 12 项病例对照研究的个体水平数据来研究这种相关性。分析了胎儿生长的两个指标——胎龄体重和最佳出生体重比例(POBW)。使用多变量逻辑回归估计研究特异性比值比(OR)和 95%置信区间(CI),并采用固定效应荟萃分析进行合并。还使用多变量逻辑回归对所有数据进行汇总分析。当可能时进行亚组分析。所有 12 项研究中均提供了 7348 例病例和 12489 例对照的胎龄体重数据,其中 3 项研究提供了 1680 例病例和 3139 例对照的 POBW 数据。荟萃分析的汇总 OR 为大于胎龄儿相对于适于胎龄儿的 1.24(95%CI:1.13,1.36),而 POBW 每增加一个标准差的 OR 为 1.16(95%CI:1.09,1.24)。汇总分析得出了类似的结果。对于小于胎龄儿,汇总和汇总 OR 分别为 0.83(95%CI:0.75,0.92)和 0.86(95%CI:0.77,0.95)。结果在按性别、种族和免疫表型定义的亚组中一致,并且当分析仅限于没有高出生体重的儿童时,结果也是一致的。加速胎儿生长与儿童 ALL 发病风险适度增加之间的关联证据确凿,与涉及胰岛素样生长因子的已知生物学机制一致。 © 2013 UICC。