Suppr超能文献

小儿急性起病神经精神综合征或神经发育障碍急性行为倒退中DNA损伤修复基因的超罕见变异

Ultrarare Variants in DNA Damage Repair Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome or Acute Behavioral Regression in Neurodevelopmental Disorders.

作者信息

Cunningham Janet L, Frankovich Jennifer, Dubin Robert A, Pedrosa Erika, Baykara Refia Nur, Schlenk Noelle Cathleen, Maqbool Shahina B, Dolstra Hedwig, Marino Jacqueline, Edinger Jacob, Shea Julia M, Laje Gonzalo, Swagemakers Sigrid M A, Sinnadurai Siamala, Zhang Zhengdong D, Lin Jhih-Rong, van der Spek Peter J, Lachman Herbert M

机构信息

Department of Medical Sciences, Psychiatry, Uppsala University, Uppsala, Sweden.

Department of Pediatrics, Division of Pediatric Allergy, Immunology, Rheumatology and Immune Behavioral Health Program, Stanford Children's Health and Stanford University School of Medicine, Palo Alto, California, USA.

出版信息

Dev Neurosci. 2024 Oct 11:1-20. doi: 10.1159/000541908.

Abstract

INTRODUCTION

Acute onset of severe psychiatric symptoms or regression may occur in children with premorbid neurodevelopmental disorders, although typically developing children can also be affected. Infections or other stressors are likely triggers. The underlying causes are unclear, but a current hypothesis suggests the convergence of genes that influence neuronal and immunological function. We previously identified 11 genes in pediatric acute-onset neuropsychiatric syndrome (PANS), in which two classes of genes related to either synaptic function or the immune system were found. Among the latter, three affect the DNA damage response (DDR): PPM1D, CHK2, and RAG1. We now report an additional 17 cases with mutations in PPM1D and other DDR genes in patients with acute onset of psychiatric symptoms and/or regression that their clinicians classified as PANS or another inflammatory brain condition.

METHODS

We analyzed genetic findings obtained from parents and carried out whole-exome sequencing on a total of 17 cases, which included 3 sibling pairs and a family with 4 affected children.

RESULTS

The DDR genes include clusters affecting p53 DNA repair (PPM1D, ATM, ATR, 53BP1, and RMRP), and the Fanconi Anemia Complex (FANCE, SLX4/FANCP, FANCA, FANCI, and FANCC). We hypothesize that defects in DNA repair genes, in the context of infection or other stressors, could contribute to decompensated states through an increase in genomic instability with a concomitant accumulation of cytosolic DNA in immune cells triggering DNA sensors, such as cGAS-STING and AIM2 inflammasomes, as well as central deficits on neuroplasticity. In addition, increased senescence and defective apoptosis affecting immunological responses could be playing a role.

CONCLUSION

These compelling preliminary findings motivate further genetic and functional characterization as the downstream impact of DDR deficits may point to novel treatment strategies.

摘要

引言

患有病前神经发育障碍的儿童可能会急性发作严重的精神症状或出现退化,不过正常发育的儿童也可能受到影响。感染或其他应激源可能是诱因。其根本原因尚不清楚,但目前有一种假说认为,影响神经元和免疫功能的基因会发生汇聚。我们之前在儿童急性起病神经精神综合征(PANS)中鉴定出了11个基因,其中发现了两类与突触功能或免疫系统相关的基因。在后者中,有三个基因影响DNA损伤反应(DDR):PPM1D、CHK2和RAG1。我们现在报告另外17例患有急性精神症状发作和/或退化的患者,其临床医生将其归类为PANS或另一种炎症性脑病,这些患者的PPM1D和其他DDR基因存在突变。

方法

我们分析了从父母那里获得的基因检测结果,并对总共17例病例进行了全外显子组测序,其中包括3对同胞和一个有4名患病儿童的家庭。

结果

DDR基因包括影响p53 DNA修复的基因簇(PPM1D、ATM、ATR、53BP1和RMRP),以及范可尼贫血复合体(FANCE、SLX4/FANCP、FANCA、FANCI和FANCC)。我们推测,在感染或其他应激源的背景下,DNA修复基因的缺陷可能会通过增加基因组不稳定性,同时免疫细胞中胞质DNA积累触发DNA传感器(如cGAS-STING和AIM2炎性小体)以及神经可塑性方面的中枢缺陷,从而导致失代偿状态。此外,衰老增加和影响免疫反应的凋亡缺陷可能也在起作用。

结论

这些引人注目的初步发现促使我们进一步开展基因和功能研究,因为DDR缺陷的下游影响可能指向新的治疗策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验