Low-grade systemic inflammation in patients with amyotrophic lateral sclerosis

Objective –  To prospectively determine the intensity of systemic low‐grade inflammation in patients with amyotrophic lateral sclerosis (ALS). Patients and methods –  Patients with ALS and matched healthy controls underwent blood tests for inflammation‐sensitive biomarkers: erythrocyte sedimentation...

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Published inActa neurologica Scandinavica Vol. 119; no. 6; pp. 383 - 389
Main Authors Keizman, D., Rogowski, O., Berliner, S., Ish-Shalom, M., Maimon, N., Nefussy, B., Artamonov, I., Drory, V. E.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.2009
Blackwell
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Summary:Objective –  To prospectively determine the intensity of systemic low‐grade inflammation in patients with amyotrophic lateral sclerosis (ALS). Patients and methods –  Patients with ALS and matched healthy controls underwent blood tests for inflammation‐sensitive biomarkers: erythrocyte sedimentation rate (ESR), quantitative fibrinogen, wide‐range C‐reactive protein (wrCRP) concentrations, leukocyte count and neutrophil‐to‐lymphocyte ratio (NLR). The correlation between these inflammatory biomarkers and disability status of the patients, expressed by the ALS Functional Rating Scale (ALSFRS‐R), was evaluated. Results –  Eighty patients with ALS and 80 matched controls were included. wrCRP, fibrinogen, ESR and NLR values were significantly elevated in patients compared with controls. There was a significant correlation between the ALSFRS‐R score and wrCRP, ESR and fibrinogen levels. This correlation persisted on sequential examinations. Conclusions –  A systemic low‐grade inflammation was detected in patients with ALS and correlated with their degree of disability. A heightened systemic inflammatory state is apparently associated with a negative prognosis in ALS.
Bibliography:ArticleID:ANE1112
istex:AB591BAF4DC295BFC8E57DD5B57B268AC67C86C6
ark:/67375/WNG-XT2MWCBT-R
Contributed equally to this study.
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ISSN:0001-6314
1600-0404
DOI:10.1111/j.1600-0404.2008.01112.x