Effect of cerebral sinus venous thrombosis and its location on cerebral blood flow: a [15O]water PET study in acute stroke patients compared to healthy volunteers.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING EJNMMI Research Pub Date : 2024-11-21 DOI:10.1186/s13550-024-01180-9
Andreas Harloff, Ganna Blazhenets, Johannes Fostitsch, Christoph Strecker, Rick Dersch, Ernst Mayerhofer, Philipp T Meyer
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Abstract

Background: Symptoms in acute cerebral sinus venous thrombosis (CSVT) are highly variable, ranging from headaches to fatal stroke, and the basis for this high inter-individual variability is poorly understood. The present study aimed to assess whether acute CSVT significantly alters regional cerebral blood flow (CBF), if findings differ from CBF patterns know from large-artery occlusion in stroke, and whether the pattern of CBF alterations depends on clot location. Therefore, we retrospectively analyzed 12 patients with acute CSVT 10.6 ± 4.6 days after symptom onset and ten healthy volunteers who underwent [15O]water PET (two scans each, 300 ± 14 MBq [15O]water). Static image datasets (15-75 s after injection; normalized to cerebellum) reflecting relative CBF (rCBF) were analyzed using voxel- and region-of-interest-based analysis (AAL3-atlas). We mirrored datasets of patients with left-sided CSVT to harmonize the affected hemisphere.

Results: Seven and five patients showed right- and left-sided CSVT, respectively. The superior sagittal sinus (SSS) was involved in 8/12 patients. CSVT patients had extensive rCBF deficits in the voxel-based analysis with accentuation in the right (ipsilateral) frontal cortex and caudate nucleus compared to controls, which were most pronounced in cortical areas in those with involvement of the SSS (8/12), and in subcortical areas in those without involvement of the SSS (4/12; p < 0.05, false discovery rate corrected). ROI-analysis demonstrated significant frontal (p = 0.01) and caudate nucleus (p = 0.008) rCBF deficits driven by patients with and without SSS occlusion, respectively.

Conclusions: [15O]water PET was able to visualize characteristic patterns of impaired rCBF, which were different from intracranial large-artery occlusion in acute ischemic stroke, and exhibited substantial rCBF alterations depending on the involvement of the SSS. Our findings provide novel insights into the effects of disturbed venous drainage on CBF in acute CSVT, which may aid in understanding the pathophysiology, and guide future therapy of acute CSVT.

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脑窦静脉血栓形成及其位置对脑血流的影响:急性脑卒中患者与健康志愿者的[15O]水 PET 研究比较。
背景:急性脑窦静脉血栓形成(CSVT)的症状变化很大,从头痛到致命性中风不等,而这种个体间高度变化的基础尚不清楚。本研究旨在评估急性 CSVT 是否会明显改变区域脑血流(CBF),评估结果是否与中风大动脉闭塞时的 CBF 模式不同,以及 CBF 改变的模式是否取决于血栓的位置。因此,我们对 12 名急性 CSVT 患者(症状出现后 10.6 ± 4.6 天)和 10 名健康志愿者进行了[15O]水 PET(各两次扫描,300 ± 14 MBq [15O]水)回顾性分析。我们使用基于体素和感兴趣区的分析方法(AAL3-atlas)分析了反映相对 CBF(rCBF)的静态图像数据集(注射后 15-75 秒;小脑归一化)。我们镜像了左侧 CSVT 患者的数据集,以统一受影响的半球:结果:分别有 7 名和 5 名患者出现右侧和左侧 CSVT。8/12例患者的上矢状窦(SSS)受累。与对照组相比,在基于体素的分析中,CSVT 患者的右侧(同侧)额叶皮层和尾状核出现了广泛的 rCBF 缺陷,在 SSS 受累的患者中,皮层区域的 rCBF 缺陷最为明显(8/12),而在 SSS 未受累的患者中,皮层下区域的 rCBF 缺陷最为明显(4/12;P 结论:[15O]水 PET 能够对 CSVT 患者的大脑皮层和皮层下区域进行分析:[15O]水 PET 能够显示 rCBF 受损的特征性模式,这不同于急性缺血性卒中的颅内大动脉闭塞,而且根据 SSS 的受累程度不同,rCBF 也有很大的改变。我们的研究结果为了解急性 CSVT 中静脉引流紊乱对 CBF 的影响提供了新的视角,有助于理解病理生理学并指导急性 CSVT 的未来治疗。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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