Correlation of clinical features and findings on cranial magnetic resonance imaging with urinary myelin basic protein-like material in patients with multiple sclerosis
Corresponding Author
Dr. John N. Whitaker
Department of Neurology, University of Alabama at Birmingham
Department of Cell Biology, University of Alabama at Birmingham
Center for Neuroimmunlogy, University of Alabama at Birmingham
Neurology and Research Services of the Birmingham Veterans Medical Center, Birmingham, AL
Department of Neurology, University of Alabama at Birmingham, UAB Station, Birmingham, AL 35294-0007Search for more papers by this authorPaula H. Williams
Department of Neurology, University of Alabama at Birmingham
Search for more papers by this authorBeverly A. Layton
Department of Neurology, University of Alabama at Birmingham
Search for more papers by this authorHenry F. McFarland
Neuroimmuinology Branch of the National Institutes of Health, Bethesda, MD
Search for more papers by this authorLael A. Stone
Neuroimmuinology Branch of the National Institutes of Health, Bethesda, MD
Search for more papers by this authorM. E. Smith
Neuroimmuinology Branch of the National Institutes of Health, Bethesda, MD
Search for more papers by this authorR. David Kachelhofer
Department of Neurology, University of Alabama at Birmingham
Search for more papers by this authorEdwin L. Bradley
Department of Biostatistics, University of Alabama at Birmingham
Search for more papers by this authorSheila Burgard
Department of Biostatistics, University of Alabama at Birmingham
Search for more papers by this authorGuojun Zhao
Division of Neurology, Vancouver General Hospital, Vancouver, British Columbia, Canada
Search for more papers by this authorDonald W. Paty
Division of Neurology, Vancouver General Hospital, Vancouver, British Columbia, Canada
Search for more papers by this authorCorresponding Author
Dr. John N. Whitaker
Department of Neurology, University of Alabama at Birmingham
Department of Cell Biology, University of Alabama at Birmingham
Center for Neuroimmunlogy, University of Alabama at Birmingham
Neurology and Research Services of the Birmingham Veterans Medical Center, Birmingham, AL
Department of Neurology, University of Alabama at Birmingham, UAB Station, Birmingham, AL 35294-0007Search for more papers by this authorPaula H. Williams
Department of Neurology, University of Alabama at Birmingham
Search for more papers by this authorBeverly A. Layton
Department of Neurology, University of Alabama at Birmingham
Search for more papers by this authorHenry F. McFarland
Neuroimmuinology Branch of the National Institutes of Health, Bethesda, MD
Search for more papers by this authorLael A. Stone
Neuroimmuinology Branch of the National Institutes of Health, Bethesda, MD
Search for more papers by this authorM. E. Smith
Neuroimmuinology Branch of the National Institutes of Health, Bethesda, MD
Search for more papers by this authorR. David Kachelhofer
Department of Neurology, University of Alabama at Birmingham
Search for more papers by this authorEdwin L. Bradley
Department of Biostatistics, University of Alabama at Birmingham
Search for more papers by this authorSheila Burgard
Department of Biostatistics, University of Alabama at Birmingham
Search for more papers by this authorGuojun Zhao
Division of Neurology, Vancouver General Hospital, Vancouver, British Columbia, Canada
Search for more papers by this authorDonald W. Paty
Division of Neurology, Vancouver General Hospital, Vancouver, British Columbia, Canada
Search for more papers by this authorAbstract
Immunoreactive material that appears to be a peptide encompassing all or a portion of residues 80 to 89 of myelin basic protein is present in normal unconcentrated urine and is increased in certain patients with multiple sclerosis (MS). Compared with normal controls, urines collected randomly from 158 MS patients or in a clinical research unit from 8 patients with MS had higher mean values of urinary MBP-like material (MBPLM). The level of MBPLM in urine showed no direct relationship to MBPLM in cerebrospinal fluid and did not correlate with clinical relapses of disease. In the other neurological disease control group (26 patients), some patients with other inflammatory diseases, but not stroke or early phase Guillain-Barré syndrome, also showed elevations. Among the subtypes of MS, those with secondary chronic progressive disease had the highest values. Urinary MBPLM showed no definite correlation with or effect of treatment with glucocorticoids and immunosuppressants except that a lower level of urinary MBPLM showed a weak relationship with improvement following treatment with methylprednisolone/prednisone. In a serial study of 8 patients with unenhanced cranial magnetic resonance imaging and 20 patients with gadolinium-enhanced cranial magnetic resonance imaging, urinary MBPLM did not show a direct correlation with new or enhancing lesions. Urinary MBPLM does not parallel acute myelin damage but appears to reflect an ongoing process, possibly linked to attempted efforts at remyelination.
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