Mean upper cervical cord area (MUCCA) measurement in long-standing multiple sclerosis: Relation to brain findings and clinical disability

Author:

Daams Marita1,Weiler Florian2,Steenwijk Martijn D3,Hahn Horst K2,Geurts Jeroen JG3,Vrenken Hugo3,van Schijndel Ronald A3,Balk Lisanne J3,Tewarie Prejaas K3,Tillema Jan-Mendelt4,Killestein Joep3,Uitdehaag Bernard MJ3,Barkhof Frederik3

Affiliation:

1. VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands

2. Fraunhofer MEVIS, Institute for Medical Image Computing, Bremen, Germany

3. Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands

4. Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands/ Mayo Clinic, Rochester, MN, USA

Abstract

Background: The majority of patients with multiple sclerosis (MS) present with spinal cord pathology. Spinal cord atrophy is thought to be a marker of disease severity, but in long-disease duration its relation to brain pathology and clinical disability is largely unknown. Objective: Our aim was to investigate mean upper cervical cord area (MUCCA) in patients with long-standing MS and assess its relation to brain magnetic resonance imaging (MRI) measures and clinical disability. Methods: MUCCA was measured in 196 MS patients and 55 healthy controls using 3DT1-weighted cervical images obtained at 3T MRI. Clinical disability was measured using the Expanded Disability Status Scale (EDSS), Nine-Hole-Peg test (9-HPT), and 25 feet Timed Walk Test (TWT). Stepwise linear regression was performed to assess the association between MUCCA and MRI measures, and between MUCCA and clinical disability. Results: MUCCA was smaller (mean 11.7%) in MS patients compared with healthy controls (72.56±9.82 and 82.24±7.80 mm2 respectively; p<0.001), most prominently in male patients. MUCCA was associated with normalized brain volume, and number of cervical cord lesions. MUCCA was independently associated with EDSS, TWT, and 9-HPT. Conclusion: MUCCA was reduced in MS patients compared with healthy controls. It provides a relevant marker for clinical disability in long-standing disease, independent of other MRI measures.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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