Wendy Klag Center for Autism and Developmental Disabilities, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Mol Psychiatry. 2024 Jan;29(1):43-53. doi: 10.1038/s41380-023-02046-7. Epub 2023 Apr 27.
There is a need to consider paternal contributions to autism spectrum disorder (ASD) more strongly. Autism etiology is complex, and heritability is not explained by genetics alone. Understanding paternal gametic epigenetic contributions to autism could help fill this knowledge gap. In the present study, we explored whether paternal autistic traits, and the sperm epigenome, were associated with autistic traits in children at 36 months enrolled in the Early Autism Risk Longitudinal Investigation (EARLI) cohort. EARLI is a pregnancy cohort that recruited and enrolled pregnant women in the first half of pregnancy who already had a child with ASD. After maternal enrollment, EARLI fathers were approached and asked to provide a semen specimen. Participants were included in the present study if they had genotyping, sperm methylation data, and Social Responsiveness Scale (SRS) score data available. Using the CHARM array, we performed genome-scale methylation analyses on DNA from semen samples contributed by EARLI fathers. The SRS-a 65-item questionnaire measuring social communication deficits on a quantitative scale-was used to evaluate autistic traits in EARLI fathers (n = 45) and children (n = 31). We identified 94 significant child SRS-associated differentially methylated regions (DMRs), and 14 significant paternal SRS-associated DMRs (fwer p < 0.05). Many child SRS-associated DMRs were annotated to genes implicated in ASD and neurodevelopment. Six DMRs overlapped across the two outcomes (fwer p < 0.1), and, 16 DMRs overlapped with previous child autistic trait findings at 12 months of age (fwer p < 0.05). Child SRS-associated DMRs contained CpG sites independently found to be differentially methylated in postmortem brains of individuals with and without autism. These findings suggest paternal germline methylation is associated with autistic traits in 3-year-old offspring. These prospective results for autism-associated traits, in a cohort with a family history of ASD, highlight the potential importance of sperm epigenetic mechanisms in autism.
需要更加强烈地考虑父亲对自闭症谱系障碍 (ASD) 的贡献。自闭症的病因很复杂,遗传率不能仅用遗传学来解释。了解父亲配子的表观遗传贡献有助于填补这一知识空白。在本研究中,我们探讨了在参加早期自闭症风险纵向研究 (EARLI) 队列的 36 个月大的儿童中,父亲的自闭症特征和精子表观基因组是否与自闭症特征有关。EARLI 是一个妊娠队列,招募并纳入了已经有自闭症儿童的妊娠前半期的孕妇。在母亲入组后,EARLI 的父亲被联系并要求提供精液样本。如果参与者有基因分型、精子甲基化数据和社会反应量表 (SRS) 评分数据,则将其纳入本研究。我们使用 CHARM 阵列对 EARLI 父亲的精液样本中的 DNA 进行了全基因组甲基化分析。SRS-一种用于评估 EARLI 父亲(n=45)和儿童(n=31)自闭症特征的 65 项问卷,用于定量评估社交沟通缺陷。我们确定了 94 个与儿童 SRS 相关的差异甲基化区域 (DMR) 和 14 个与父亲 SRS 相关的 DMR(fwer p<0.05)。许多与儿童 SRS 相关的 DMR 被注释为与 ASD 和神经发育相关的基因。两个结果之间有 6 个 DMR 重叠(fwer p<0.1),并且有 16 个 DMR 与 12 个月大的儿童自闭症特征的先前发现重叠(fwer p<0.05)。与儿童 SRS 相关的 DMR 包含 CpG 位点,这些位点在有和没有自闭症的个体的死后大脑中被独立发现存在甲基化差异。这些发现表明,父亲生殖系甲基化与 3 岁子女的自闭症特征有关。在一个有 ASD 家族史的队列中,对自闭症相关特征的这些前瞻性结果突出了精子表观遗传机制在自闭症中的潜在重要性。