Gialloreti Leonardo Emberti, Benvenuto Arianna, Benassi Francesca, Curatolo Paolo
Department of Biomedicine and Prevention, University of Rome ''Tor Vergata", Rome, Italy; Centre for Communication and Neurorehabilitation Research - CNAPP, Rome, Italy.
Department of Neuroscience, Pediatric Neurology Unit, Tor Vergata University of Rome, Italy.
Med Hypotheses. 2014 Jun;82(6):713-8. doi: 10.1016/j.mehy.2014.03.011. Epub 2014 Mar 13.
The etiology of Autism Spectrum Disorders (ASDs) continues to be elusive. While ASDs have been shown to be heritable, several environmental co-factors, such as, e.g. pre- or perinatal adverse events, could play a role in the pathogenesis of the disorder as well. Prevalence of ASDs appears to have increased in the last three decades, but the causes of this surge are not fully understood. As perinatal adverse events have increased as well, they have been regarded as logical contributors to the risen prevalence of ASDs. Over the last three decades there has been also a considerable increase in the rates of induced labor and caesarean sections (CS). However, even if a causal association between CS and ASDs increase has been suggested, it has not yet been proven. Nevertheless, we hypothesize here that such an association is actual and that it might help to explain a part of the increase in ASD diagnoses. Our assumption is based on the wider epidemiological picture of ASDs and CS, as well as on the possible biological plausibility of this correlation, by postulating potential epigenetic and neurobiological mechanisms underpinning this relationship. Today, several observations point toward the existence of epigenetic dysregulation in ASDs and this raises the issue of the role of environmental factors in bringing about epigenetic modifications. Epigenetic dysregulations in some brain neuropeptide systems could play a role in the behavioral dysfunctions of ASDs. Particularly, some evidence suggests a dysregulation of the oxytocinergic system in autistic brains. Perinatal alterations of oxytocin (OT) can also have life-long lasting effects on the development of social behaviors. Within the perinatal period, various processes, like pitocin infusion or CS, can alter the OT balance in the newborn; OT dysregulation could then interact with genetic factors, leading ultimately to the development of ASDs. Large long-term prospective studies are needed to identify causal pathways for ASDs and examine whether and how (epi-)genetic susceptibility interacts with obstetric risk factors in the development of ASDs. A better understanding of such a potential interplay could become paradigmatic for a wide range of genetic-environmental interactions in ASDs.
自闭症谱系障碍(ASD)的病因仍然难以捉摸。虽然已证明ASD具有遗传性,但一些环境辅助因素,如产前或围产期不良事件,也可能在该疾病的发病机制中起作用。在过去三十年中,ASD的患病率似乎有所上升,但这种激增的原因尚未完全了解。由于围产期不良事件也有所增加,它们被认为是ASD患病率上升的合理因素。在过去三十年中,引产和剖宫产(CS)的发生率也有相当大的增加。然而,即使有人提出CS与ASD增加之间存在因果关系,但尚未得到证实。尽管如此,我们在此假设这种关联是真实的,并且它可能有助于解释ASD诊断增加的部分原因。我们的假设基于ASD和CS更广泛的流行病学情况,以及这种相关性可能的生物学合理性,通过假设支撑这种关系的潜在表观遗传和神经生物学机制。如今,一些观察结果表明ASD中存在表观遗传失调,这引发了环境因素在引起表观遗传修饰中所起作用的问题。某些脑内神经肽系统的表观遗传失调可能在ASD的行为功能障碍中起作用。特别是,一些证据表明自闭症大脑中的催产素能系统失调。围产期催产素(OT)的改变也可能对社会行为的发展产生终身影响。在围产期内,各种过程,如缩宫素输注或剖宫产,可改变新生儿的OT平衡;OT失调然后可能与遗传因素相互作用,最终导致ASD的发展。需要进行大型长期前瞻性研究来确定ASD的因果途径,并检查(表观)遗传易感性在ASD发展中是否以及如何与产科危险因素相互作用。更好地理解这种潜在的相互作用可能成为ASD中广泛的基因 - 环境相互作用的范例。