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Geurts, Jeroen J.G.

https://orcid.org/0000-0003-1896-3748

Mayo Clinic

Amsterdam Neuroscience

Citations 2

Assessment of lesions on magnetic resonance imaging in multiple sclerosis: practical guidelines
Filippi, Massimo , Preziosa, Paolo , Banwell, Brenda , Barkhof, Frederik , Ciccarelli, Olga , Stefano, Nicola De , Geurts, Jeroen J.G. , Paul, Friedemann , Reich, Daniel S. , Toosy, Ahmed , Wattjes, Mike P. , Yousry, Tarek , Gass, Achim , Lubetzki, Catherine , Weinshenker, Brian G. , Rocca, Maria A. , Weinshenker, Brian G , Filippi, Massimo , Barkhof, Frederik , Paul, Friedemann , Rocca, Maria A , Ciccarelli, Olga , Traboulsee, Anthony

Brain | May 13, 2019 | Volume: 142 | Issue: 7 | Pages: 1858-1875

10.1093/brain/awz144 Get It

Abstract MRI has improved the diagnostic work-up of multiple sclerosis, but inappropriate image interpretation and application of MRI diagnostic criteria contribute to misdiagnosis. Some diseases, now recognized as conditions distinct from multiple sclerosis, may satisfy the MRI criteria for multiple sclerosis (e.g. neuromyelitis optica spectrum disorders, Susac syndrome), thus making the diagnosis of multiple sclerosis more challenging, especially if biomarker testing (such as serum anti-AQP4 antibodies) is not informative. Improvements in MRI technology contribute and promise to better define the typical features of multiple sclerosis lesions (e.g. juxtacortical and periventricular location, cortical involvement). Greater understanding of some key aspects of multiple sclerosis pathobiology has allowed the identification of characteristics more specific to multiple sclerosis (e.g. central vein sign, subpial demyelination and lesional rims), which are not included in the current multiple sclerosis diagnostic criteria. In this review, we provide the clinicians and researchers with a practical guide to enhance the proper recognition of multiple sclerosis lesions, including a thorough definition and illustration of typical MRI features, as well as a discussion of red flags suggestive of alternative diagnoses. We also discuss the possible place of emerging qualitative features of lesions which may become important in the near future.
Mean upper cervical cord area (MUCCA) measurement in long-standing multiple sclerosis: Relation to brain findings and clinical disability
Daams, Marita , Weiler, Florian , Steenwijk, Martijn D. , Hahn, Horst K. , Geurts, Jeroen J.G. , Schijndel, Ronald A. van , Balk, Lisanne J. , Tewarie, Prejaas , Tillema, Jan‐Mendelt , Killestein, Joep , Uitdehaag, Bernard M.J. , Barkhof, Frederik , Vrenken, Hugo , Barkhof, Frederik

Multiple Sclerosis Journal | May 9, 2014 | Volume: 20 | Issue: 14 | Pages: 1860-1865

10.1177/1352458514533399 Get It

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 mm 2 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.