Cerebrospinal fluid and serum antibodies against neurofilaments in patients with amyotrophic lateral sclerosis
Background: The aim of the study was to assess autoimmune involvement in amyotrophic lateral sclerosis (ALS). Methods: We measured IgG antibodies against light (NFL) and medium (NFM) subunits of neurofilaments using ELISA in paired cerebrospinal fluid (CSF) and serum samples from 38 ALS patients a...
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Published in | European journal of neurology Vol. 17; no. 4; pp. 562 - 566 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.04.2010
John Wiley & Sons, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Background: The aim of the study was to assess autoimmune involvement in amyotrophic lateral sclerosis (ALS).
Methods: We measured IgG antibodies against light (NFL) and medium (NFM) subunits of neurofilaments using ELISA in paired cerebrospinal fluid (CSF) and serum samples from 38 ALS patients and 20 controls.
Results: Serum levels of anti‐NFL were higher in ALS patients than in controls (P < 0.005). Serum anti‐NFL antibodies and intrathecal anti‐NFM antibodies were related to patient disability (serum anti‐NFL: P < 0.05; intrathecal anti‐NFM: P < 0.05). Anti‐NFL levels were significantly correlated with anti‐NFM levels in ALS (P < 0.001) and the control group (P < 0.0001) in the CSF, but not in serum. Anti‐NFL and anti‐NFM antibodies significantly correlated between serum and CSF in the ALS group (anti‐NFL: P < 0.0001; anti‐NFM: P < 0.001) and in the control group (anti‐NFL: P < 0.05; anti‐NFM: P < 0.05).
Conclusions: Autoimmune humoral response to neurocytoskeletal proteins is associated with ALS. |
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Bibliography: | istex:AEC102915881CBD8820015F2385CEDBE541001DF ark:/67375/WNG-JVFCK1DG-G ArticleID:ENE2853 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1351-5101 1468-1331 |
DOI: | 10.1111/j.1468-1331.2009.02853.x |