Lumour-Mensah Tabitha, Korrick Susan, Lemos Bernardo, Mazumdar Maitreyi
Department of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA 02115, United States of America.
Department of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA 02115, United States of America; Channing Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, United States of America.
Neurochem Int. 2025 Oct;189:106033. doi: 10.1016/j.neuint.2025.106033. Epub 2025 Aug 11.
Spina bifida is a complex and multifactorial congenital defect driven by both genetic and environmental factors. As such, epigenetic studies of spina bifida present an opportunity to study the joint contribution of both genes and the environment in the development of this disorder. This review focuses specifically on epigenetic research that may help us to understand the ways in which dysregulation of the epigenome and downstream cellular processes can confer increased risk of spina bifida. To do so, we discuss the epigenetic regulation of genes linked to spina bifida risk among children born with the disorder and their parents as well as evidence from experimental studies. We also discuss pathways necessary for normal neural tube development and specific documented dysregulation of these pathways in individuals with spina bifida. We conclude that the epigenome plays an important role in spina bifida etiology and should be further studied in additional populations, and tissue types, as well as cellular and animal models.
脊柱裂是一种由遗传和环境因素共同驱动的复杂多因素先天性缺陷。因此,脊柱裂的表观遗传学研究为研究基因和环境在这种疾病发生发展中的共同作用提供了契机。本综述特别关注表观遗传学研究,这些研究可能有助于我们理解表观基因组失调和下游细胞过程增加脊柱裂风险的方式。为此,我们讨论了与脊柱裂风险相关基因在患有该疾病的儿童及其父母中的表观遗传调控,以及来自实验研究的证据。我们还讨论了正常神经管发育所需的途径以及脊柱裂患者中这些途径的特定记录失调情况。我们得出结论,表观基因组在脊柱裂病因学中起着重要作用,应在更多人群、组织类型以及细胞和动物模型中进一步研究。