Department of Advanced Medical and Surgical Sciences (DAMSS), University of Campania "Luigi Vanvitelli", 80138, Naples, Italy.
Channing Division of Network Medicine and the Division of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Matern Child Health J. 2024 Apr;28(4):617-630. doi: 10.1007/s10995-023-03886-z. Epub 2024 Feb 26.
The ability to identify early epigenetic signatures underlying the inheritance of cardiovascular risk, including trans- and intergenerational effects, may help to stratify people before cardiac symptoms occur.
Prospective and retrospective cohorts and case-control studies focusing on DNA methylation and maternal/paternal effects were searched in Pubmed from 1997 to 2023 by using the following keywords: DNA methylation, genomic imprinting, and network analysis in combination with transgenerational/intergenerational effects.
Maternal and paternal exposures to traditional cardiovascular risk factors during critical temporal windows, including the preconceptional period or early pregnancy, may perturb the plasticity of the epigenome (mainly DNA methylation) of the developing fetus especially at imprinted loci, such as the insulin-like growth factor type 2 (IGF2) gene. Thus, the epigenome is akin to a "molecular archive" able to memorize parental environmental insults and predispose an individual to cardiovascular diseases onset in later life. Direct evidence for human transgenerational epigenetic inheritance (at least three generations) of cardiovascular risk is lacking but it is supported by epidemiological studies. Several blood-based association studies showed potential intergenerational epigenetic effects (single-generation studies) which may mediate the transmittance of cardiovascular risk from parents to offspring.
In this narrative review, we discuss some relevant examples of trans- and intergenerational epigenetic associations with cardiovascular risk. In our perspective, we propose three network-oriented approaches which may help to clarify the unsolved issues regarding transgenerational epigenetic inheritance of cardiovascular risk and provide potential early biomarkers for primary prevention.
识别心血管风险遗传的早期表观遗传特征的能力,包括跨代和代际效应,可能有助于在出现心脏症状之前对人群进行分层。
从 1997 年到 2023 年,通过使用以下关键词在 Pubmed 中搜索前瞻性和回顾性队列研究和病例对照研究,重点关注 DNA 甲基化和母系/父系效应:DNA 甲基化、基因组印迹和网络分析与跨代/代际效应相结合。
母体和父体在关键时间窗口(包括受孕前或早期妊娠)接触传统心血管危险因素,可能会破坏发育中胎儿的表观基因组(主要是 DNA 甲基化)的可塑性,特别是在印迹基因座,如胰岛素样生长因子 2 (IGF2) 基因。因此,表观基因组类似于一个“分子档案”,能够记住父母的环境伤害,并使个体易患晚年心血管疾病。人类跨代表观遗传遗传(至少三代)的心血管风险的直接证据是缺乏的,但得到了流行病学研究的支持。一些基于血液的关联研究显示出潜在的代际表观遗传效应(单代研究),这可能介导了从父母到子女的心血管风险的传递。
在这篇叙述性综述中,我们讨论了一些与心血管风险相关的跨代和代际表观遗传关联的相关例子。在我们看来,我们提出了三种面向网络的方法,这些方法可能有助于阐明关于心血管风险跨代表观遗传遗传的未解决问题,并为一级预防提供潜在的早期生物标志物。