Literature DB >> 30219498

Longitudinal assessment of clinical and inflammatory markers in patients with amyotrophic lateral sclerosis.

Laura de Godoy Rousseff Prado1, Natalia Pessoa Rocha2, Leonardo Cruz de Souza3, Isabella Carolina Santos Bicalho4, Rodrigo Santiago Gomez5, Mauro Vidigal-Lopes6, Nayara Felicidade Tomaz Braz7, Érica Leandro Marciano Vieira8, Antônio Lúcio Teixeira9.   

Abstract

OBJECTIVE: To evaluate potential associations between clinical features and inflammatory markers in patients with amyotrophic lateral sclerosis (ALS).
METHODS: A consecutive series of 68 patients (39 males and 29 females) with sporadic ALS were subjected to a comprehensive clinical assessment and blood draw. A subset of these patients underwent a new assessment within 6-12 months after the baseline visit. In addition, a group of 62 subjects composed by age and sex-matched healthy subjects (38 males and 24 females) was enrolled in this study. Peripheral blood was drawn and plasma levels of chemokines and cytokines were measured by cytometric bead array and enzyme-linked immunosorbent assay.
RESULTS: Our sample was composed by patients with ALS with an average age of 58 (±12.3) years old and 3 (±2.7) years of disease length at the baseline visit. Patients with ALS presented increased plasma levels of interleukin (IL)-6 and IL-8 in comparison with controls. After multivariate analysis, higher levels of IL-6 and lower levels of IL-2 were significantly associated with increased likelihood of ALS diagnosis. When evaluating the subset of patients assessed longitudinally, we did not find any significant difference in the levels of inflammatory markers between the two time points. Older age at ALS onset was the only factor associated with a faster rate of disease progression.
CONCLUSIONS: IL-6 levels could discriminate between ALS and controls and may be regarded as a potential biomarker of ALS diagnosis. An increase in IL-2 levels was associated with a protective effect on the odds of ALS diagnosis. Older age at ALS onset predicted a fast rate of disease progression.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; Biomarkers; Chemokines; Cytokines; Inflammation

Mesh:

Substances:

Year:  2018        PMID: 30219498     DOI: 10.1016/j.jns.2018.08.033

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  5 in total

1.  Circulating miR-181 is a prognostic biomarker for amyotrophic lateral sclerosis.

Authors:  Iddo Magen; Nancy Sarah Yacovzada; Eran Yanowski; Anna Coenen-Stass; Julian Grosskreutz; Ching-Hua Lu; Linda Greensmith; Andrea Malaspina; Pietro Fratta; Eran Hornstein
Journal:  Nat Neurosci       Date:  2021-10-28       Impact factor: 24.884

Review 2.  Are Circulating Cytokines Reliable Biomarkers for Amyotrophic Lateral Sclerosis?

Authors:  Laura Moreno-Martinez; Ana Cristina Calvo; María Jesús Muñoz; Rosario Osta
Journal:  Int J Mol Sci       Date:  2019-06-05       Impact factor: 5.923

3.  Neuroprotective Fragment C of Tetanus Toxin Modulates IL-6 in an ALS Mouse Model.

Authors:  Laura Moreno-Martinez; Miriam de la Torre; María J Muñoz; Pilar Zaragoza; José Aguilera; Ana C Calvo; Rosario Osta
Journal:  Toxins (Basel)       Date:  2020-05-17       Impact factor: 4.546

Review 4.  Blood-based biomarkers of inflammation in amyotrophic lateral sclerosis.

Authors:  Kim A Staats; David R Borchelt; Malú Gámez Tansey; James Wymer
Journal:  Mol Neurodegener       Date:  2022-01-24       Impact factor: 14.195

Review 5.  Neuroinflammation in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia and the Interest of Induced Pluripotent Stem Cells to Study Immune Cells Interactions With Neurons.

Authors:  Elise Liu; Léa Karpf; Delphine Bohl
Journal:  Front Mol Neurosci       Date:  2021-12-14       Impact factor: 5.639

  5 in total

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