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January 28, 2003; 60 (2) Articles

Multiple sclerosis

Neurofilament light chain antibodies are correlated to cerebral atrophy

M.J. Eikelenboom, A. Petzold, R.H.C. Lazeron, E. Silber, M. Sharief, E.J. Thompson, F. Barkhof, G. Giovannoni, C.H. Polman, B.M.J. Uitdehaag
First published January 28, 2003, DOI: https://doi.org/10.1212/01.WNL.0000041496.58127.E3
M.J. Eikelenboom
MD
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A. Petzold
MD
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R.H.C. Lazeron
MD
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E. Silber
MD
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M. Sharief
MD PhD
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E.J. Thompson
MD PhD
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F. Barkhof
MD PhD
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G. Giovannoni
MD PhD
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C.H. Polman
MD PhD
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B.M.J. Uitdehaag
MD PhD
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Citation
Multiple sclerosis
Neurofilament light chain antibodies are correlated to cerebral atrophy
M.J. Eikelenboom, A. Petzold, R.H.C. Lazeron, E. Silber, M. Sharief, E.J. Thompson, F. Barkhof, G. Giovannoni, C.H. Polman, B.M.J. Uitdehaag
Neurology Jan 2003, 60 (2) 219-223; DOI: 10.1212/01.WNL.0000041496.58127.E3

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Abstract

Objective: To evaluate markers of axonal damage in CSF and serum of patients with different subtypes of MS in relation to measures of disease progression on MRI.

Methods: In 51 patients with MS (21 relapsing-remitting, 20 secondary progressive, 10 primary progressive), levels of heavy and light neurofilaments (NfH and NfL) and antibodies to neurofilaments (anti-NfL and -NfH) as well as the total immunoglobulin G (IgG) were analyzed. MRI analysis included T2 hyperintense, T1 hypointense, and gadolinium enhancing lesions and markers of cerebral atrophy (ventricular and parenchymal fractions).

Results: For the total group, correlations were found between the anti-NfL index and the parenchymal fraction (PF) (r = −0.51, p < 0.001), T2 lesion load (r = 0.41, p < 0.05), ventricular fraction (r = 0.37, p < 0.05), and T1 lesion load (r = 0.37, p < 0.05). For the anti-NfH index, a correlation was found with the PF (r = −0.39, p < 0.05). No correlations were found between the IgG index and MRI measures.

Conclusions: Intrathecal production of anti-NfL antibodies may serve as a marker of tissue damage, particularly axonal loss, in MS.

  • Received July 25, 2002.
  • Accepted September 18, 2002.
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