Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, 75 Mikras Asias Str, 11527, Athens, Greece.
Clinical Epidemiology Unit, Department of Medicine, Karolinska Institute, Stockholm, Sweden.
Eur J Epidemiol. 2018 Oct;33(10):965-976. doi: 10.1007/s10654-018-0402-z. Epub 2018 May 14.
Advanced parental age has been associated with adverse health effects in the offspring including childhood (0-14 years) acute lymphoblastic leukemia (ALL), as reported in our meta-analysis of published studies. We aimed to further explore the association using primary data from 16 studies participating in the Childhood Leukemia International Consortium. Data were contributed by 11 case-control (CC) studies (7919 cases and 12,942 controls recruited via interviews) and five nested case-control (NCC) studies (8801 cases and 29,690 controls identified through record linkage of population-based health registries) with variable enrollment periods (1968-2015). Five-year paternal and maternal age increments were introduced in two meta-analyses by study design using adjusted odds ratios (OR) derived from each study. Increased paternal age was associated with greater ALL risk in the offspring (OR 1.05, 95% CI 1.00-1.11; OR 1.04, 95% CI 1.01-1.07). A similar positive association with advanced maternal age was observed only in the NCC results (OR 0.99, 95% CI 0.91-1.07, heterogeneity I = 58%, p = 0.002; OR 1.05, 95% CI 1.01-1.08). The positive association between parental age and risk of ALL was most marked among children aged 1-5 years and remained unchanged following mutual adjustment for the collinear effect of the paternal and maternal age variables; analyses of the relatively small numbers of discordant paternal-maternal age pairs were not fully enlightening. Our results strengthen the evidence that advanced parental age is associated with increased childhood ALL risk; collinearity of maternal with paternal age complicates causal interpretation. Employing datasets with cytogenetic information may further elucidate involvement of each parental component and clarify underlying mechanisms.
高龄父母与后代的不良健康影响有关,包括儿童(0-14 岁)急性淋巴细胞白血病(ALL),这在我们对已发表研究的荟萃分析中已有报道。我们旨在使用参加儿童白血病国际联盟的 16 项研究的原始数据进一步探索这种关联。数据来自 11 项病例对照(CC)研究(通过访谈招募了 7919 例病例和 12942 例对照)和 5 项巢式病例对照(NCC)研究(通过基于人群的健康登记处的记录链接确定了 8801 例病例和 29690 例对照),这些研究的入组时间不同(1968-2015 年)。我们根据每项研究得出的调整后的优势比(OR),通过研究设计在两项荟萃分析中引入了五年的父龄和母龄递增。较高的父龄与后代 ALL 风险增加相关(OR 1.05,95%CI 1.00-1.11;OR 1.04,95%CI 1.01-1.07)。仅在 NCC 结果中观察到与母亲年龄增长相关的类似正相关(OR 0.99,95%CI 0.91-1.07,异质性 I=58%,p=0.002;OR 1.05,95%CI 1.01-1.08)。在 1-5 岁的儿童中,父母年龄与 ALL 风险之间的正相关最为明显,并且在对父龄和母龄变量的共线性效应进行相互调整后,这种相关性仍然不变;对数量相对较少的不一致的父母年龄对的分析并没有完全说明问题。我们的结果加强了高龄父母与儿童 ALL 风险增加有关的证据;母亲年龄与父亲年龄的共线性使因果关系的解释变得复杂。使用具有细胞遗传学信息的数据集可能会进一步阐明每个父母成分的作用,并阐明潜在的机制。