Magnetic resonance imaging-based changes in vascular morphology and cerebral perfusion in subacute ischemic stroke

Author:

Kufner Anna123ORCID,Khalil Ahmed A1345ORCID,Galinovic Ivana1,Kellner Elias6,Mekle Ralf1,Rackoll Torsten178ORCID,Boehm-Sturm Philipp1910ORCID,Fiebach Jochen B12,Flöel Agnes11112,Ebinger Martin113,Endres Matthias123814,Nave Alexander H12314

Affiliation:

1. Charité–Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Center for Stroke Research Berlin, Berlin, Germany

2. Klinik und Hochschulambulanz für Neurologie, Charité – Universitätsmedizin Berlin, Berlin, Germany

3. Berlin Institute of Health, Berlin, Germany

4. School of Mind and Brain, Humboldt Universität zu Berlin, Berlin, Germany

5. Department of Neurology, Max Plank Institute for Human Cognitive and Brain Sciences, Leipzig, Germany

6. Department of Radiology, Medical Physics, University Medical Center Freiburg, Freiburg, Germany

7. QUEST Center for Transforming Biomedical Research, Berlin Institute of Health, Berlin, Germany

8. ExcellenceCluster NeuroCure, Charite-Universitätsmedizin Berlin, Berlin, Germany

9. NeuroCure Cluster of Excellence and Charité Core Facility 7T Experimental MRIs, Charité – Universitätsmedizin Berlin, Berlin, Germany

10. Department of Experimental Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany

11. Department of Neurology, University Medicine Greifswald, Greifswald, Germany

12. German Center for Neurodegenerative Diseases, Partner Site Rostock/Greifswald, Greifswald, Germany

13. Department of Neurology, Medical Park Berlin Humboldtmühle, Berlin, Germany

14. German Centre for Cardiovascular Research (DZHK), Berlin, Germany

Abstract

MRI-based vessel size imaging (VSI) allows for in-vivo assessment of cerebral microvasculature and perfusion. This exploratory analysis of vessel size (VS) and density (Q; both assessed via VSI) in the subacute phase of ischemic stroke involved sixty-two patients from the BAPTISe cohort (‘Biomarkers And Perfusion--Training-Induced changes after Stroke’) nested within a randomized controlled trial (intervention: 4-week training vs. relaxation). Relative VS, Q, cerebral blood volume (rCBV) and –flow (rCBF) were calculated for: ischemic lesion, perilesional tissue, and region corresponding to ischemic lesion on the contralateral side (mirrored lesion). Linear mixed-models detected significantly increased rVS and decreased rQ within the ischemic lesion compared to the mirrored lesion (coefficient[standard error]: 0.2[0.08] p = 0.03 and −1.0[0.3] p = 0.02, respectively); lesion rCBF and rCBV were also significantly reduced. Mixed-models did not identify time-to-MRI, nor training as modifying factors in terms of rVS or rQ up to two months post-stroke. Larger lesion VS was associated with larger lesion volumes (β 34, 95%CI 6.2–62; p = 0.02) and higher baseline NIHSS (β 3.0, 95%CI 0.49–5.3;p = 0.02), but was not predictive of six-month outcome. In summary, VSI can assess the cerebral microvasculature and tissue perfusion in the subacute phases of ischemic stroke, and may carry relevant prognostic value in terms of lesion volume and stroke severity.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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