Revisiting the Pathophysiology of Intracranial Hemorrhage in Fetuses with Chiari II Malformation: Novel Imaging Biomarkers of Disease Severity?

Hui Shi, Daniela Prayer, Patric Kienast, Farjad Khalaveh, Johannes Tischer, Julia Binder, Michael Weber, Marlene Stuempflen, Gregor Kasprian
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Abstract

Background and purpose: Intracranial hemorrhage (ICH) has emerged as a notable concern in Chiari II malformation (CM II), yet its origins and clinical implications remain elusive. This study aims to validate the in utero prevalence of ICH in CM II and investigate contributing factors, and visualize the findings in a network format.

Materials and methods: A single-center retrospective review of fetal MRI scans obtained in fetuses with CM II (presenting January 2007 to December 2022) was performed for ICH utilizing EPI-T2* blood-sensitive sequence. Fetuses with aqueduct stenosis (AS) were included as a control group. The incidence of ICH and corresponding gestational ages were compared between CM II and AS cases, and morphometric measurements (inner/outer CSF spaces, posterior fossa, venous structure) were compared among the 4 1:1 age-matched groups: CM II+ICH, CM II-ICH, AS+ICH, and AS-ICH. Additionally, a co-occurrence network was constructed to visualize associations between phenotypic features in ICH cases.

Results: A total of 101 fetuses with CM II and 90 controls with AS at a median gestational age of 24.4 weeks and 22.8 weeks (P = .138) were included. Prevalence of ICH in fetuses with CM II was higher compared with the AS cases (28.7% versus 18.9%, P = .023), accompanied by congested veins (deep vein congestion mainly in young fetuses, and cortical veins may also be affected in older fetuses). ICH was notably correlated with specific anatomic features, essentially characterized by reduced outer CSF spaces and clivus-supraocciput angle. The co-occurrence network analysis reveals complex connections including bony defects, small posterior fossa dimensions, vermis ectopia, reduced CSF spaces, as well as venous congestion and venous sinus stenosis as pivotal components within the network.

Conclusions: The high prevalence of ICH-detected by fetal MRI-among fetuses with CM emphasizes the pathophysiologic importance of venous congestion, ICH, and vasogenic edema. As indicators of disease severity, these features may serve as helpful additional imaging biomarkers for the identification of potential candidates for fetal surgery.

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重新审视Chiari II畸形胎儿颅内出血的病理生理学--疾病严重程度的新型成像生物标志物?
背景和目的:颅内出血(ICH)已成为Chiari II畸形(CM II)的一个值得关注的问题,但其起源和临床影响仍难以确定。本研究旨在验证 ICH 在 CM II 胎儿期的发病率,调查诱发因素,并以网络形式将研究结果可视化:一项单中心回顾性研究利用 EPI-T2* 血敏感序列对出现 CM II 的胎儿(2007 年 1 月至 2022 年 12 月)的胎儿 MRI 扫描进行了 ICH 检查。患有导水管狭窄(AS)的胎儿作为对照组。比较了 CM II 和 AS 病例的 ICH 发生率和相应的胎龄,并比较了四个 1:1 年龄匹配组的形态测量结果(CSF 内/外间隙、后窝、静脉结构):CM II+ICH、CM II-ICH、AS+ICH 和 AS-ICH。此外,还构建了共现网络,以直观显示 ICH 病例表型特征之间的关联:结果:共纳入101例CM II胎儿和90例AS对照组胎儿,中位胎龄分别为24.4周和22.8周(P=.138)。与强直性脊柱炎病例相比,CM II 胎儿的 ICH 患病率更高(28.7% 对 18.9%,P=.023),同时伴有静脉充血(深静脉充血主要发生在年轻胎儿,高龄胎儿的皮质静脉也可能受到影响)。ICH 与特定的解剖学特征显著相关,主要特征是脑脊液外间隙缩小和颅骨-上枕角缩小。共现网络分析揭示了复杂的联系,包括骨缺损、后窝尺寸小、蚓部异位、脑脊液空间缩小以及静脉充血和静脉窦狭窄,这些都是网络中的关键组成部分:结论:通过胎儿磁共振成像检测到的 ICH 在 CM 胎儿中的高发病率强调了静脉充血、ICH 和血管源性水肿的病理生理重要性。作为疾病严重程度的指标,这些特征可作为识别胎儿手术潜在候选者的额外影像生物标志物:CM=卡氏II型畸形;AS=导水管狭窄;ICH=颅内出血。
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