Characterizing the time course of cerebrovascular reactivity in multiple sclerosis. Issue 3 (14th February 2022)

• Record Type: Journal Article
• Authors: Lincoln, John A.; Hasan, Khader M.; Gabr, Refaat E.; Wolinsky, Jerry S.
• Is Part Of: Journal of neuroimaging. Volume 32:Issue 3(2022)
• Page Start: 430
• Page End: 435
• Publication Date: 2022-02-14
• Subjects: acetazolamide -- cerebral perfusion -- cerebrovascular reactivity -- multiple sclerosis -- time course; Diagnostic imaging -- Periodicals; Nervous system -- Diseases -- Diagnosis -- Periodicals; Imagerie pour le diagnostic -- Périodiques; Système nerveux -- Maladies -- Diagnostic -- Périodiques; Imagerie médicale; Neuroimagerie; Neurologie; Système nerveux; Périodique électronique (Descripteur de forme); Ressource Internet (Descripteur de forme); 616.804754
• DOI: 10.1111/jon.12979
• Languages: English
• ISSNs: 1051-2284

Abstract

Abstract: Background and Purpose: Changes in cerebral perfusion occur early in relapsing and progressive multiple sclerosis (MS) patients, though whether cerebral blood flow (CBF) can be altered by therapy is unknown. We sought to characterize the time course of change in CBF (cerebral vascular reactivity [CVR]), following intravenous (IV) acetazolamide (ACZ) in whole brain and within various gray and white matter brain regions in MS patients. Methods: We enrolled five relapsing MS patients on injectable therapies. Participants received a 1000 mg IV bolus of ACZ and CBF was measured using pseudocontinuous arterial spin labeling MRI. To quantify differences in time course between patients, we calculated the numerical integration of CVR over time using the trapezoidal rule to estimate area under the curve (AUC(CVR) ). Results: A change in whole brain CBF of 30%‐65% was seen in all participants at 15 minutes after ACZ challenge. CBF increases >20% above baseline were sustained for 90 minutes within whole‐brain, normal‐appearing white matter and total T2‐hyperintense lesioned tissue. AUC(CVR) values for both gray (cortical and deep gray matter) and white (normal‐appearing and T2‐lesioned) matter regions were similar between patients. Conclusion: Our findings show a prolonged time course in vascular reactivity after ACZ stimulus in MS patients with a similar time course for both gray and white matter brain regions, including in previously injured tissue. Our preliminary results suggest that blood flow can be augmented in the established MS lesion suggesting that even previously injured tissue might be responsive to treatment.