• J Neuroimaging · Jul 2021

    Intracranial atherosclerotic disease mechanistic subtypes drive hypoperfusion patterns.

    • Song J Kim, Jose M Morales, Shadi Yaghi, Tristan Honda, Fabien Scalzo, Jason D Hinman, Radoslav Raychev, Latisha K Sharma, Edward Feldmann, Jose G Romano, Shyam Prabhakaran, and David S Liebeskind.
    • Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, California, USA.
    • J Neuroimaging. 2021 Jul 1; 31 (4): 686-690.

    Background And PurposeIn symptomatic intracranial atherosclerotic stenosis (ICAS), borderzone infarct pattern and perfusion mismatch are associated with increased risk of recurrent strokes, which may reflect the shared underlying mechanism of hypoperfusion distal to the intracranial atherosclerosis. Accordingly, we hypothesized a correlation between hypoperfusion volumes and ICAS infarct patterns based on the respective underlying mechanistic subtypes.MethodsWe conducted a retrospective analysis of consecutive symptomatic ICAS cases, acute strokes due to subocclusive (50%-99%) intracranial stenosis. The following mechanistic subtypes were assigned based on the infarct pattern on the diffusion-weighted imaging: Branch occlusive disease (BOD), internal borderzone (IBZ), and thromboembolic (TE). Perfusion parameters, obtained concurrently with the MRI, were studied in each group.ResultsA total of 42 patients (57% women, mean age 71 ± 13 years old) with symptomatic ICAS received MRI within 24 h of acute presentation. Fourteen IBZ, 11 BOD, and 17 TE patterns were identified. IBZ pattern yielded higher total Tmax > 4 s and Tmax > 6 s perfusion delay volumes, as well as corresponding Tmax  > 4 s and Tmax  > 6 s mismatch volume, compared to BOD. TE pattern exhibited greater median Tmax  > 6 s hypoperfusion delay in volume compared to BOD. In IBZ versus TE, the volume difference between Tmax > 4 s and Tmax > 6 s (Δ Tmax  > 4 s - Tmax  > 6 s) was substantially greater.ConclusionICAS infarct patterns, in keeping with their respective underlying mechanisms, may correlate with distinct perfusion profiles.© 2021 American Society of Neuroimaging.

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