Oakley L L, Kristjansson D, Munthe-Kaas M C, Nguyen H T, Lee Y, Hanevik H I, Romundstad L B, Lyle R, Håberg S E
Centre for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway.
Non-Communicable Disease Epidemiology Unit, London School of Hygiene and Tropical Medicine, London, UK.
Hum Reprod. 2025 Feb 1;40(2):382-390. doi: 10.1093/humrep/deae285.
Does the risk of childhood cancer following ARTs vary by sex?
In this registry-based study, some childhood cancers showed positive sex- and age-specific associations in children conceived using certain ART modalities, which were not evident in overall combined analyses.
The relationship between ART and risk of childhood cancer has shown diverse outcomes in prior research. Studies examining whether there are sex differences in childhood cancer risk after ART conception are lacking.
STUDY DESIGN, SIZE, DURATION: This registry-based cohort study included all children born in Norway between 1984 and 2022 (n = 2 255 025), followed until 31 December 2023.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Children were identified via the Medical Birth Registry of Norway, and information was extracted on whether they were conceived via ART (defined as IVF/ICSI). Of the 2 255 025 children included in the study, 53 694 were ART-conceived. Birth records were linked to the Cancer Registry of Norway. Childhood cancer was defined as a cancer diagnosis according to the International Classification of Childhood Cancer Third Edition (ICCC-3) before the age of 18 years. Cox regression models were used to estimate the age- and sex-specific risk of cancer for ART-conceived children compared to children not conceived via ART.
Among all children, 0.25% had a cancer diagnosis before the age of 18 years. The cumulative incidence of cancer was higher in children conceived by ART (IVF/ICSI) than in those not conceived via ART (21.5 vs 17.5 per 100 000 person-years, P = 0.04), and especially higher in boys conceived with ICSI or after cryopreserved embryo transfer. When combining all age groups, both sexes and all cancer types, there was little evidence of increased cancer risk with ART (adjusted hazard ratio (aHR) 1.13, 95% CI 0.94-1.36). However, differences were found when stratifying by age and sex. From age 5-9 years, ART-conceived children had a higher overall risk of cancer (aHR 1.53, 95% CI 1.06-2.20), with a slightly higher estimate in boys (aHR 1.73, 95% CI 1.09-2.74), than in girls (aHR 1.28, 95% CI 0.70-2.33). The risk was not higher up to age 5 years, or after age 10 years. In combined analyses, there was no overall increased risk after ICSI. When stratifying by sex, a higher risk was seen after ICSI for boys (aHR 1.69, 95% CI 1.18-2.42), but not for girls (aHR 0.65, 95% CI 0.37-1.16). The combined risk after cryopreservation (aHR 1.42, 95% CI 0.95-2.13) was driven by a higher risk in boys (aHR 1.79, 95% CI 1.09-2.94), while no evidence of an association was found in girls (aHR 1.01, 95% CI 0.50-2.03). No increased risk was seen with IVF or after fresh transfer for either boys or girls.
LIMITATIONS, REASONS FOR CAUTION: Childhood cancer is a rare outcome, and some analyses of cancer subtypes were likely underpowered.
Results from this large registry-based study suggest that addressing age- and sex-specific differences in the risk of childhood cancer following ART conception reveals increased risks for certain groups. Our findings require further study with consideration of possible underlying sex-specific mechanisms related to ART and different childhood cancers.
STUDY FUNDING/COMPETING INTEREST(S): This work was funded by: the Research Council of Norway through its Centres of Excellence Funding Scheme (project number 262700); the Norwegian Cancer Association (project number 244291); and the Norwegian Institute of Public Health. The funding agencies had no role in the conceptualization, design, data collection, analysis, decision to publish, or preparation of the manuscript. The authors declare no conflict of interests.
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辅助生殖技术(ARTs)后儿童患癌风险是否因性别而异?
在这项基于登记处的研究中,某些ART方式受孕的儿童中,一些儿童癌症显示出特定性别和年龄的正相关,而在总体综合分析中并不明显。
先前的研究表明ART与儿童患癌风险之间的关系呈现出不同的结果。缺乏关于ART受孕后儿童癌症风险是否存在性别差异的研究。
研究设计、规模、持续时间:这项基于登记处的队列研究纳入了1984年至2022年在挪威出生的所有儿童(n = 2255025),随访至2023年12月31日。
参与者/材料、设置、方法:通过挪威医疗出生登记处识别儿童,并提取他们是否通过ART(定义为体外受精/卵胞浆内单精子注射)受孕的信息。在纳入研究的2255025名儿童中,53694名是通过ART受孕的。出生记录与挪威癌症登记处相关联。儿童癌症定义为根据《国际儿童癌症分类第三版》(ICCC - 3)在18岁之前的癌症诊断。使用Cox回归模型估计与未通过ART受孕的儿童相比,通过ART受孕的儿童患癌的年龄和性别特异性风险。
在所有儿童中,0.25%在18岁之前被诊断患有癌症。通过ART(体外受精/卵胞浆内单精子注射)受孕的儿童的癌症累积发病率高于未通过ART受孕的儿童(每100000人年分别为21.5和17.5,P = 0.04),尤其是通过卵胞浆内单精子注射或冷冻胚胎移植受孕的男孩中更高。当合并所有年龄组、两性和所有癌症类型时,几乎没有证据表明ART会增加患癌风险(调整后风险比(aHR)1.13,95%置信区间0.94 - 1.36)。然而,按年龄和性别分层时发现了差异。在5至9岁年龄段,通过ART受孕的儿童总体患癌风险更高(aHR 1.53,95%置信区间1.06 - 2.20),男孩的估计值略高于女孩(aHR 1.73,95%置信区间1.09 - 2.74)(aHR 1.28,95%置信区间0.70 - 2.33)。在5岁之前或10岁之后风险没有更高。在综合分析中,卵胞浆内单精子注射后总体风险没有增加。按性别分层时,卵胞浆内单精子注射后男孩的风险更高(aHR 1.69,95%置信区间1.18 - 2.42),但女孩没有(aHR 0.65,95%置信区间0.37 - 1.16)。冷冻保存后的综合风险(aHR 1.42,95%置信区间0.95 - 2.13)是由男孩的较高风险驱动的(aHR 1.79,95%置信区间1.09 - 2.94),而在女孩中未发现关联证据(aHR 1.01,95%置信区间0.50 - 2.03)。无论是男孩还是女孩,体外受精或新鲜移植后风险均未增加。
局限性、谨慎原因:儿童癌症是一种罕见的结果,对癌症亚型的一些分析可能效力不足。
这项基于大型登记处的研究结果表明,考虑ART受孕后儿童癌症风险的年龄和性别特异性差异会发现某些群体的风险增加。我们的研究结果需要进一步研究,考虑与ART和不同儿童癌症相关的可能潜在性别特异性机制。
研究资金/利益冲突:这项工作由以下机构资助:挪威研究理事会通过其卓越中心资助计划(项目编号262700);挪威癌症协会(项目编号244291);以及挪威公共卫生研究所。资助机构在概念化、设计、数据收集、分析、决定发表或稿件准备方面没有作用。作者声明无利益冲突。
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