van Niftrik C H B, Sebök M, Muscas G, Wegener S, Luft A R, Stippich C, Regli L, Fierstra J
Department of Neurosurgery, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Clinical Neuroscience Center, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Front Physiol. 2021 Jun 24;12:645157. doi: 10.3389/fphys.2021.645157. eCollection 2021.
Wallerian degeneration and diaschisis are considered separate remote entities following ischemic stroke. They may, however, share common neurophysiological denominators, since they are both related to disruption of fiber tracts and brain atrophy over time. Therefore, with advanced multimodal neuroimaging, we investigate Wallerian degeneration and its association with diaschisis.
In order to determine different characteristics of Wallerian degeneration, we conducted examinations on seventeen patients with chronic unilateral ischemic stroke and persisting large vessel occlusion, conducting high-resolution anatomical magnetic resonance imaging (MRI) and blood oxygenation-level dependent cerebrovascular reactivity (BOLD-CVR) tests, as well as Diamox (O)-HO-PET hemodynamic examinations. Wallerian degeneration was determined using a cerebral peduncle asymmetry index (% difference of volume of ipsilateral and contralateral cerebral peduncle) of more than two standard deviations away from the average of age-matched, healthy subjects (Here a cerebral peduncle asymmetry index > 11%). Diaschisis was derived from BOLD-CVR to assess the presence of ipsilateral thalamus diaschisis and/or crossed cerebellar diaschisis.
Wallerian degeneration, found in 8 (47%) subjects, had a strong association with ipsilateral thalamic volume reduction ( = 0.60) and corticospinal-tract involvement of stroke ( < 0.001). It was also associated with ipsilateral thalamic diaschisis ( = 0.021), No cerebral peduncular hemodynamic differences were found in patients with Wallerian degeneration. In particular, no CBF decrease or BOLD-CVR impairment was found.
We show a strong association between Wallerian degeneration and ipsilateral thalamic diaschisis, indicating a structural pathophysiological relationship.
华勒氏变性和交叉性小脑失联络被认为是缺血性中风后的两个独立的远隔性病变。然而,它们可能具有共同的神经生理学特征,因为它们都与纤维束的中断和随时间推移的脑萎缩有关。因此,借助先进的多模态神经影像学技术,我们对华勒氏变性及其与交叉性小脑失联络的关系进行了研究。
为了确定华勒氏变性的不同特征,我们对17例慢性单侧缺血性中风且存在持续性大血管闭塞的患者进行了检查,包括高分辨率解剖磁共振成像(MRI)、血氧水平依赖性功能磁共振脑血管反应性(BOLD-CVR)测试以及乙酰唑胺(O)-HO-PET血流动力学检查。使用大脑脚不对称指数(同侧和对侧大脑脚体积的百分比差异)来确定华勒氏变性,该指数偏离年龄匹配的健康受试者平均值超过两个标准差(此处大脑脚不对称指数>11%)。交叉性小脑失联络通过BOLD-CVR来评估同侧丘脑交叉性小脑失联络和/或对侧小脑交叉性小脑失联络的存在情况。
在8例(47%)受试者中发现了华勒氏变性,其与同侧丘脑体积减小(r = 0.60)和中风累及皮质脊髓束(p < 0.001)密切相关。它还与同侧丘脑交叉性小脑失联络有关(p = 0.021)。在患有华勒氏变性的患者中未发现大脑脚血流动力学差异。特别是,未发现脑血流量减少或BOLD-CVR受损。
我们发现华勒氏变性与同侧丘脑交叉性小脑失联络之间存在密切关联,表明存在结构病理生理关系。