Urhoj Stine Kjaer, Raaschou-Nielsen Ole, Hansen Anne Vinkel, Mortensen Laust Hvas, Andersen Per Kragh, Nybo Andersen Anne-Marie
Section of Social Medicine, Department of Public Health, University of Copenhagen, Oster Farimagsgade 5, POB 2099, DK-1014 Copenhagen K, Denmark.
Danish Cancer Society Research Center, Strandboulevarden 49, DK-2100 Copenhagen O, Denmark.
Int J Cancer. 2017 Jun 1;140(11):2461-2472. doi: 10.1002/ijc.30677. Epub 2017 Mar 23.
Cancer initiation is presumed to occur in utero for many childhood cancers and it has been hypothesized that advanced paternal age may have an impact due to the increasing number of mutations in the sperm DNA with increasing paternal age. We examined the association between paternal age and specific types of childhood cancer in offspring in a large nationwide cohort of 1,904,363 children born in Denmark from 1978 through 2010. The children were identified in the Danish Medical Birth Registry and were linked to information from other national registers, including the Danish Cancer Registry. In total, 3,492 children were diagnosed with cancer before the age of 15 years. The adjusted hazard ratio of childhood cancer according to paternal age was estimated using Cox proportional hazards regressions. We found a 13% (95% confidence interval: 4-23%) higher hazard rate for every 5 years advantage in paternal age for acute lymphoblastic leukemia, while no clear association was found for acute myeloid leukemia (hazard ratio pr. 5 years = 1.02, 95% confidence interval: 0.80-1.30). The estimates for neoplasms in the central nervous system suggested a lower hazard rate with higher paternal age (hazard ratio pr. 5 years = 0.92, 95% confidence interval: 0.84-1.01). No clear associations were found for the remaining childhood cancer types. The findings suggest that paternal age is moderately associated with a higher rate of childhood acute lymphoblastic leukemia, but not acute myeloid leukemia, in offspring, while no firm conclusions could be made for other specific cancer types.
许多儿童癌症被认为在子宫内就开始发生,并且有假说认为,由于随着父亲年龄的增加精子DNA中的突变数量增多,父亲年龄偏大可能会产生影响。我们在一个大型全国队列中研究了父亲年龄与子代特定类型儿童癌症之间的关联,该队列包含1978年至2010年在丹麦出生的1,904,363名儿童。这些儿童在丹麦医疗出生登记处被识别,并与包括丹麦癌症登记处在内的其他国家登记处的信息相链接。总共有3492名儿童在15岁之前被诊断患有癌症。根据父亲年龄,使用Cox比例风险回归估计儿童癌症的调整后风险比。我们发现,父亲年龄每大5岁,急性淋巴细胞白血病的风险率就会高出13%(95%置信区间:4%-23%),而急性髓细胞白血病未发现明显关联(每5年的风险比 = 1.02,95%置信区间:0.80-1.30)。中枢神经系统肿瘤的估计结果表明,父亲年龄越大,风险率越低(每5年的风险比 = 0.92,95%置信区间:0.84-1.01)。其余儿童癌症类型未发现明显关联。研究结果表明,父亲年龄与子代儿童急性淋巴细胞白血病的较高发病率存在中度关联,但与急性髓细胞白血病无关,而对于其他特定癌症类型则无法得出确凿结论。