Intensity Score of Vessel Wall Contrast Enhancement in MRI Allows Prediction of Disease Progression in Moyamoya Angiopathy

Author:

Shih-Yüng Wang Sophie12ORCID,Hauser Till-Karsten3,Haas Patrick12,Tellermann Jonas12,Hurth Helene12,Ernemann Ulrike3,Tatagiba Marcos12,Bender Benjamin3,Khan Nadia24,Roder Constantin12ORCID

Affiliation:

1. Department of Neurosurgery and Neurotechnology, Eberhard Karls University of Tübingen, Tübingen, Germany;

2. Center for Moyamoya and Cerebral Revascularization, Eberhard Karls University of Tübingen, Tübingen, Germany;

3. Department of Neuroradiology, Eberhard Karls University of Tübingen, Tübingen, Germany;

4. Moyamoya Center, University Children's Hospital and University of Zurich, Zurich, Switzerland

Abstract

BACKGROUND AND OBJECTIVES: The underlying pathophysiological cause of moyamoya angiopathy (MMA) is still unclear. High-resolution vessel wall imaging has become a useful tool. The aim was to study vessel wall contrast-enhancement (VW-CE) as an imaging marker to predict disease progression in MMA. METHODS: Patients with MMA, who had undergone serial contrast-enhanced high-resolution MRI with concomitant and follow-up digital subtraction angiography, were analyzed retrospectively. VW-CE was semiquantified by measurement of the signal intensity of the vessel wall in in contrast-enhanced high-resolution MRI. A comparative quotient with the contrast-intensity of the pituitary stalk was calculated and graded accordingly from grade 1 to 5. VW-CE status was correlated with disease status, stroke, cerebrovascular reactivity in CO2-triggered blood-oxygen level-dependent MRI, angiographic disease progression, revascularization surgery, and follow-up imaging. RESULTS: Forty eight patients met the inclusion criteria. N = 56 MRI and digital subtraction angiography time-intervals were evaluated for 12 vessel sections per hemisphere each (N = 1344). N = 38 (79%) patients showed VW-CE and N = 10 (21%) did not. VW-CE was only observed in the terminal internal carotid artery and the proximal circle of Willis (N = 96/1344). Notably, patients with VW-CE significantly more often presented with acute infarction in the concomitant MRI. The incidence of angiographically proven disease progression was significantly associated with the incidence of VW-CE, and time to disease progression was earlier in higher grades of VW-CE compared with lower grades. CONCLUSION: VW-CE is a semiquantifiable marker for disease activity in patients with MMA and associated with disease progression and increased risk of stroke. VW-CE analysis can be routinely performed in patients with MMA to estimate the risk for disease progression and stroke.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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