Sarić Nemanja, Ishibashi Nobuyuki
Center for Neuroscience Research, Children's National Medical Center, Washington, DC, United States.
Department of Pediatrics, Pharmacology and Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC, United States.
Front Genet. 2024 Aug 8;15:1460228. doi: 10.3389/fgene.2024.1460228. eCollection 2024.
Congenital heart disease (CHD) has, despite significant improvements in patient survival, increasingly become associated with neurological deficits during infancy that persist into adulthood. These impairments afflict a wide range of behavioral domains including executive function, motor learning and coordination, social interaction, and language acquisition, reflecting alterations in multiple brain areas. In the past few decades, it has become clear that CHD is highly genetically heterogeneous, with large chromosomal aneuploidies and copy number variants (CNVs) as well as single nucleotide polymorphisms (SNPs) being implicated in CHD pathogenesis. Intriguingly, many of the identified loss-of-function genetic variants occur in genes important for primary cilia integrity and function, hinting at a key role for primary cilia in CHD. Here we review the current evidence for CHD primary cilia associated genetic variants, their independent functions during cardiac and brain development and their influence on behavior. We also highlight the role of environmental exposures in CHD, including stressors such as surgical factors and anesthesia, and how they might interact with ciliary genetic predispositions to determine the final neurodevelopmental outcome. The multifactorial nature of CHD and neurological impairments linked with it will, on one hand, likely necessitate therapeutic targeting of molecular pathways and neurobehavioral deficits shared by disparate forms of CHD. On the other hand, strategies for better CHD patient stratification based on genomic data, gestational and surgical history, and CHD complexity would allow for more precise therapeutic targeting of comorbid neurological deficits.
尽管先天性心脏病(CHD)患者的生存率有了显著提高,但在婴儿期与之相关的神经功能缺损却日益增多,并持续至成年期。这些损伤影响广泛的行为领域,包括执行功能、运动学习与协调、社交互动和语言习得,反映出多个脑区的改变。在过去几十年里,已明确CHD具有高度的遗传异质性,大的染色体非整倍体和拷贝数变异(CNV)以及单核苷酸多态性(SNP)都与CHD的发病机制有关。有趣的是,许多已鉴定出的功能丧失性遗传变异发生在对初级纤毛完整性和功能至关重要的基因中,这暗示了初级纤毛在CHD中起关键作用。在此,我们综述了目前关于CHD初级纤毛相关遗传变异的证据、它们在心脏和脑发育过程中的独立功能以及对行为的影响。我们还强调了环境暴露在CHD中的作用,包括手术因素和麻醉等应激源,以及它们如何与纤毛遗传易感性相互作用以决定最终的神经发育结果。一方面,CHD及其相关神经功能缺损的多因素性质可能需要针对不同形式CHD共有的分子途径和神经行为缺损进行治疗靶向。另一方面,基于基因组数据、妊娠和手术史以及CHD复杂性进行更好的CHD患者分层的策略,将有助于更精确地针对合并的神经功能缺损进行治疗靶向。