Hubert A, Szöke A, Leboyer M, Schürhoff F
Pôle de psychiatrie du CHU de Créteil, groupe hospitalier Henri-Mondor-Albert-Chenevier, AP-HP, 40, rue Mesly, 94000 Créteil, France.
Encephale. 2011 Jun;37(3):199-206. doi: 10.1016/j.encep.2010.12.005. Epub 2011 Apr 2.
Schizophrenia is an aetiologically heterogeneous syndrome, with a strong genetic component. Despite a reduced fertility in this disorder, its prevalence is maintained and could be explained by de novo genetic mutations. Advanced paternal age (APA) is a major source of new mutations in human beings and could thus be associated with an increased risk of developing schizophrenia in offspring. New mutations related to APA have been implicated as a cause of sporadic cases in several autosomal dominant diseases and also in neurodevelopmental diseases, autism, intellectual disabilities, and social functioning. The aim of the present study was to summarize the results of studies investigating the role of APA, and to discuss some interpretations.
All relevant studies were identified through the National Library of Medicine (PubMed(®) database). Keywords used for research were "age" and "schizophrenia" linked to "paternal or father". We have identified and analysed eight cohort studies, five case-control studies, two meta-analyses, and one review concerning different father's mutations potentially transmitted, two studies comparing paternal age at conception between sporadic versus familial cases of schizophrenia. All studies selected have been published between 2000 and 2009.
After controlling for several confounding factors including maternal age, the relative risk of schizophrenia increased from 1.84 to 4.62 in offspring of fathers with an older age of fatherhood. Mother's age showed no significant effects after adjusting for paternal age. There was a significant association between paternal age and risk of developing schizophrenia, there was a weaker association with psychosis.
The results of these different studies are confirmed by two recent meta-analyses which found an increased risk of schizophrenia in offspring of fathers older than 35 years. Two main hypotheses could explain these results. The first one is based on the presence of new mutations in the spermatogonia, possibly because of accumulating replication errors in spermatogonial cell lines. This hypothesis is confirmed by Malaspina et al. (2002) [19], who found that patients without a family history of schizophrenia had significantly older fathers than probands with a positive family history of schizophrenia. However, this result has not been confirmed by other studies, and paternal age effect could be also explained by a mechanism called imprinting, which is a form of gene regulation. The second hypothesis is based on the fact that fathers with schizophrenia spectrum personality disorder, known to be genetically related to schizophrenia, could have an advanced age at conception. However, regarding this hypothesis, advanced maternal age at conception should be a risk factor for schizophrenia, and this is not the case. Thus, the first hypothesis seems more plausible than the second. APA has been identified as a risk factor for other psychiatric disorders such as autism, bipolar disorder, obsessive-compulsive disorder, and phobia, and thus seems to be a non-specific risk factor. Furthermore, its association with impaired neurocognitive outcomes during infancy and childhood in normal populations raises the question of the phenotype linked to APA.
APA at conception appears to be a risk factor for schizophrenia. This risk factor probably interacts with genetic factors in a gene-environment interaction. To date, there is no validated cut-off at which the risk is significantly increased in offspring. In the future, studies could benefit from analyzing the phenotype related to APA.
精神分裂症是一种病因异质性综合征,具有很强的遗传成分。尽管该疾病患者的生育能力有所下降,但其患病率却保持稳定,这可能是由新生基因突变所致。父亲高龄(advanced paternal age,APA)是人类新突变的一个主要来源,因此可能与后代患精神分裂症的风险增加有关。与APA相关的新突变已被认为是几种常染色体显性疾病以及神经发育疾病、自闭症、智力障碍和社会功能障碍等散发病例的病因。本研究的目的是总结有关APA作用的研究结果,并讨论一些解释。
通过美国国立医学图书馆(PubMed®数据库)检索所有相关研究。用于检索的关键词是与“父亲或爸爸”相关联的“年龄”和“精神分裂症”。我们识别并分析了八项队列研究、五项病例对照研究、两项荟萃分析以及一篇关于不同潜在可传递的父亲突变的综述,两项比较精神分裂症散发病例与家族病例受孕时父亲年龄的研究。所有入选研究均发表于2000年至2009年之间。
在控制了包括母亲年龄在内的多个混杂因素后,父亲生育年龄较大的后代患精神分裂症的相对风险从1.84增加到4.62。调整父亲年龄后,母亲年龄未显示出显著影响。父亲年龄与患精神分裂症的风险之间存在显著关联,与精神病的关联较弱。
最近的两项荟萃分析证实了这些不同研究的结果,这两项分析发现父亲年龄超过35岁的后代患精神分裂症的风险增加。有两个主要假说来解释这些结果。第一个基于精原细胞中新突变的存在,这可能是由于精原细胞系中累积的复制错误所致。Malaspina等人(2002年)[19]证实了这一假说,他们发现无精神分裂症家族史的患者的父亲比有精神分裂症阳性家族史的先证者的父亲年龄大得多。然而,其他研究并未证实这一结果,父亲年龄效应也可以用一种称为印记的机制来解释,这是一种基因调控形式。第二个假说是基于这样一个事实,即患有精神分裂症谱系人格障碍(已知与精神分裂症有遗传关系)的父亲受孕时年龄可能较大。然而,关于这一假说,母亲受孕时年龄较大也应该是精神分裂症的一个风险因素,但实际并非如此。因此,第一个假说似乎比第二个更合理。APA已被确定为其他精神疾病如自闭症、双相情感障碍、强迫症和恐惧症的一个风险因素,因此似乎是一个非特异性风险因素。此外,它与正常人群婴儿期和儿童期神经认知结果受损的关联引发了与APA相关的表型问题。
受孕时的APA似乎是精神分裂症的一个风险因素。这个风险因素可能在基因-环境相互作用中与遗传因素相互作用。迄今为止,尚无经过验证的临界值,超过该临界值后代的风险会显著增加。未来,研究可能会受益于对与APA相关表型的分析。