利用磁共振成像对梅尼埃病患者的面部神经和前庭神经进行形态学评估。

Wilhelm H Flatz, Annika Henneberger-Kunz, Regina Schinner, Ullrich Müller-Lisse, Maximilian Reiser, Birgit Ertl-Wagner
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引用次数: 0

摘要

背景和目的:梅尼埃病(MD)是一种病因不明的疾病,涉及遗传易感性、自身免疫过程、病毒感染、细胞凋亡和氧化应激。本研究旨在利用水肿-MRI(FLAIR)进行形态学评估,研究 MD 患者第七和第八颅神经的潜在差异:使用 3T 磁共振成像扫描仪,采集建构干扰-稳态(CISS)和三维-FLAIR-反转恢复(FLAIR)序列。我们评估了从小脑角到内耳道底的第七和第八颅神经的形态计量学,并对未受影响侧和受影响侧进行了比较。此外,我们还研究了研究结果与症状持续时间的关系,并评估了 FLAIR-imaging 在颅神经形态测量中的可行性:结果:共纳入了 53 名有单侧症状的 MD 患者。经过统计分析,受影响一侧与未受影响一侧的第七和第八颅神经形态变化无明显差异。对不同症状持续时间的患者进行的形态学评估也无明显差异。使用水肿-MRI-序列(FLAIR)进行的形态学评估与已有的高度T2加权成像(CISS)形态学评估相比没有显著差异:我们的数据发现,单侧多发性硬化症患者临床上未受影响的一侧和受影响的一侧的神经形态测量没有差异,与症状持续时间也没有任何关联。这与之前发现的临床特征与内淋巴水肿之间的相关性形成了鲜明对比。临床症状出现前的疾病过程可能是一种解释。使用水肿-MRI-Sequences对脑神经进行形态学评估非常实用,能提供与T2加权成像相似的结果,提高了患者的舒适度,缩短了核磁共振成像扫描时间:缩写:CN=耳蜗神经;CPA=小脑角;CSA=横截面积;FN=面神经;IAC=内耳道;IVN=下前庭神经;LD=长径;MD=梅尼埃病;SD=短径;SVN=上前庭神经。
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Morphometric evaluation of facial and vestibulocochlear nerves using magnetic resonance imaging in patients with Menière's disease.

Background and purpose: Menière's disease (MD) is a condition of unknown etiology, involving genetic predisposition, autoimmune processes, viral infections, cellular apoptosis, and oxidative stress. This study aimed to investigate potential differences in the VIIth and VIIIth cranial nerves in MD patients using Hydrops-MRI (FLAIR) for morphometric evaluations.

Materials and methods: Using a 3T MRI scanner, constructive-interference-in-steady-state (CISS) and 3D-FLAIR-inversionrecovery (FLAIR) sequences were acquired. We evaluated the morphometrics of the VIIth and VIIIth cranial nerves from the cerebellopontine angle to the internal auditory canal fundus, comparing the non-affected and affected sides. Furthermore, we examined the findings in relation to symptom duration and evaluated feasibility of FLAIR-imaging in morphometry of cranial nerves.

Results: A total of 53 MD patients with unilateral symptoms were included. After statistical analysis, no significant differences were found regarding morphometric changes in the affected side compared to the non-affected side of the VIIth and VIIIth cranial nerves. There was also no significant difference between morphometric evaluations of patients with different symptom durations. The morphometric evaluation using Hydrops-MRI-Sequences (FLAIR) showed no significant difference compared to established morphometric highly T2-weighted imaging (CISS).

Conclusions: Our data found no differences in nerve morphometry between clinically non-affected and affected sides in unilateral MD patients, nor any correlation with symptom duration. This contrasts with previous findings of correlations between clinical features and endolymphatic hydrops. A disease process starting before clinical symptom onset could be a possible explanation. Morphometric evaluation of brain nerves using Hydrops-MRI-Sequences is practical and provides similar results to T2-weighted imaging, improving patient comfort and reducing MRI scan time.

Abbreviations: CN = cochlear nerve; CPA = cerebellopontine angle; CSA = cross-sectional area; FN = facial nerve; IAC = internal auditory canal; IVN = inferior vestibular nerve; LD = long diameter; MD = Menière's disease; SD = short diameter; SVN = superior vestibular nerve.

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