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Lack of Correlation Between Cortical Demyelination and White Matter Pathologic Changes in Multiple Sclerosis
Lars Bö, MD, PhD;
Jeroen J. G. Geurts, PhD;
Paul van der Valk, MD, PhD;
Chris Polman, MD, PhD;
Frederik Barkhof, MD, PhD
Arch Neurol. 2007;64(1):76-80.
Background Histopathologic studies have shown that subpial cortical demyelination is extensive in chronic multiple sclerosis (MS).
Objective To study whether subpial cortical demyelination in MS is associated with focal or diffuse white matter (WM) pathologic features on magnetic resonance imaging (MR imaging).
Design Comparison of postmortem MR imaging findings with histopathologic findings.
Setting Brain donations from a general community.
Patients Three patients with MS with extensive cortical demyelination and 3 patients with minor cortical demyelination were selected from an MS autopsy data set. The postmortem MR imaging and histopathologic data of the patients were compared.
Main Outcome Measures Two observers blinded to the results of each other assessed the presence, extent, and distribution of focal and diffuse pathologic changes in WM by MR imaging and by histopathology.
Results Extensive subpial demyelination was not associated with a significant increase in the area of focal and diffuse WM pathologic changes as assessed by Luxol fast blue histochemistry or by MR imaging or with the presence or extent of juxtacortical abnormalities on MR imaging.
Conclusions The lack of association of MS gray matter demyelination with diffuse or focal WM changes indicates that gray matter demyelination in MS occurs largely independent of WM pathologic changes. The extent or distribution of WM abnormalities cannot be used to identify extensive cortical demyelination in the clinical setting.
Author Affiliations: Departments of Pathology (Drs Bö and van der Valk), Radiology (Drs Geurts and Barkhof), and Neurology (Dr Polman), MS Center Amsterdam, VU University Medical Center, Amsterdam, the Netherlands; and National Competence Center for Multiple Sclerosis, Department of Neurology, Haukeland University Hospital, University of Bergen, Bergen, Norway (Dr Bö).
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ABSTRACT
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