Reichenberg Abraham, Gross Raz, Weiser Mark, Bresnahan Michealine, Silverman Jeremy, Harlap Susan, Rabinowitz Jonathan, Shulman Cory, Malaspina Dolores, Lubin Gad, Knobler Haim Y, Davidson Michael, Susser Ezra
Department of Psychiatry and Seaver Center for Autism Research, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY 10029, USA.
Arch Gen Psychiatry. 2006 Sep;63(9):1026-32. doi: 10.1001/archpsyc.63.9.1026.
Maternal and paternal ages are associated with neurodevelopmental disorders.
To examine the relationship between advancing paternal age at birth of offspring and their risk of autism spectrum disorder (ASD).
Historical population-based cohort study.
Identification of ASD cases from the Israeli draft board medical registry.
We conducted a study of Jewish persons born in Israel during 6 consecutive years. Virtually all men and about three quarters of women in this cohort underwent draft board assessment at age 17 years. Paternal age at birth was obtained for most of the cohort; maternal age was obtained for a smaller subset. We used the smaller subset (n = 132 271) with data on both paternal and maternal age for the primary analysis and the larger subset (n = 318 506) with data on paternal but not maternal age for sensitivity analyses.
Information on persons coded as having International Classification of Diseases, 10th Revision ASD was obtained from the registry. The registry identified 110 cases of ASD (incidence, 8.3 cases per 10 000 persons), mainly autism, in the smaller subset with complete parental age data.
There was a significant monotonic association between advancing paternal age and risk of ASD. Offspring of men 40 years or older were 5.75 times (95% confidence interval, 2.65-12.46; P<.001) more likely to have ASD compared with offspring of men younger than 30 years, after controlling for year of birth, socioeconomic status, and maternal age. Advancing maternal age showed no association with ASD after adjusting for paternal age. Sensitivity analyses indicated that these findings were not the result of bias due to missing data on maternal age.
Advanced paternal age was associated with increased risk of ASD. Possible biological mechanisms include de novo mutations associated with advancing age or alterations in genetic imprinting.
父母年龄与神经发育障碍有关。
研究子代出生时父亲年龄增长与其患自闭症谱系障碍(ASD)风险之间的关系。
基于历史人群的队列研究。
从以色列征兵委员会医疗登记处识别ASD病例。
我们对连续6年在以色列出生的犹太人进行了一项研究。该队列中几乎所有男性和大约四分之三的女性在17岁时接受了征兵委员会评估。获得了该队列中大多数人的父亲生育年龄;获得了较小一部分人的母亲生育年龄。我们使用有父母年龄数据的较小子集(n = 132271)进行主要分析,并使用有父亲年龄但无母亲年龄数据的较大子集(n = 318506)进行敏感性分析。
从登记处获取被编码为患有《国际疾病分类》第10版ASD的人员信息。在有完整父母年龄数据的较小子集中,登记处识别出110例ASD病例(发病率为每10000人中有8.3例),主要为自闭症。
父亲年龄增长与ASD风险之间存在显著的单调关联。在控制出生年份、社会经济地位和母亲年龄后,40岁及以上男性的子代患ASD的可能性是30岁以下男性子代的5.75倍(95%置信区间,2.65 - 12.46;P <.001)。在调整父亲年龄后,母亲年龄增长与ASD无关联。敏感性分析表明,这些发现不是由于母亲年龄数据缺失导致的偏差结果。
父亲年龄较大与ASD风险增加有关。可能的生物学机制包括与年龄增长相关的新发突变或基因印记改变。