Centre for Social Evolution, Department of Biology, University of Copenhagen, Copenhagen, Denmark Department of Pathology, The University of Melbourne, Parkville, VIC 3010, Australia Present address: Centre for Systems Genomics, School of BioSciences, The University of Melbourne, Parkville, VIC 3010, Australia.
Centre for Social Evolution, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Evol Med Public Health. 2016 Sep 16;2016(1):286-98. doi: 10.1093/emph/eow023. Print 2016.
Effects of maternal and paternal age on offspring autism and schizophrenia risks have been studied for over three decades, but inconsistent risks have often been found, precluding well-informed speculation on why these age-related risks might exist.
To help clarify this situation we analysed a massive single population sample from Denmark including the full spectrum of autistic and schizophrenic disorders (eliminating between-study confounding), used up to 30 follow-up years, controlled for over 20 potentially confounding factors and interpret the ultimate causation of the observed risk patterns using generally accepted principles of parent-offspring conflict and life-history theory.
We evaluated the effects of paternal age, maternal age and parental age difference on offspring mental disorders and found consistently similar risk patterns for related disorders and markedly different patterns between autistic and schizophrenic disorders. Older fathers and mothers both conferred increased risk for autistic but not schizophrenic disorders, but autism risk was reduced in younger parents and offspring of younger mothers had increased risk for many schizophrenic disorders. Risk for most disorders also increased when parents were more dissimilarly aged. Monotonically increasing autism risk is consistent with mutation accumulation as fathers' age, but this explanation is invalid for schizophrenic disorders, which were not related to paternal age and were negatively correlated with maternal age.
We propose that the observed maternally induced risk patterns ultimately reflect a shifting ancestral life-history trade-off between current and future reproduction, mediated by an initially high but subsequently decreasing tendency to constrain foetal provisioning as women proceed from first to final pregnancy.
研究表明,母亲和父亲的年龄对后代自闭症和精神分裂症的风险有超过三十年的影响,但往往会发现不一致的风险,这使得无法对为什么这些与年龄相关的风险可能存在进行明智的推测。
为了帮助澄清这种情况,我们分析了丹麦的一个大规模的单一人群样本,其中包括自闭症和精神分裂症的全部谱系(消除了研究之间的混杂),使用了长达 30 年的随访时间,控制了 20 多个潜在的混杂因素,并使用普遍接受的亲子冲突和生活史理论的原则来解释观察到的风险模式的最终因果关系。
我们评估了父亲年龄、母亲年龄和父母年龄差异对后代精神障碍的影响,发现与自闭症相关的障碍存在一致相似的风险模式,而自闭症和精神分裂症之间存在明显不同的模式。较老的父亲和母亲都会增加自闭症的风险,但不会增加精神分裂症的风险,而年轻的父母会降低自闭症的风险,年轻母亲的后代会增加许多精神分裂症的风险。当父母年龄差异较大时,风险也会增加。自闭症风险的单调增加与父亲年龄的突变积累一致,但这种解释对于精神分裂症是无效的,因为精神分裂症与父亲年龄无关,与母亲年龄呈负相关。
我们提出,观察到的由母亲引起的风险模式最终反映了当前和未来生殖之间的祖先生活史权衡的转变,这种转变是由女性从第一次怀孕到最后一次怀孕时最初较高但随后逐渐降低的限制胎儿供应的倾向介导的。