journal article Sep 19, 2012

Alterations of signaling pathways in muscle tissues of patients with amyotrophic lateral sclerosis

Muscle & Nerve Vol. 46 No. 6 pp. 856-860 · Wiley
View at Publisher Save 10.1002/mus.23411
Abstract
AbstractIntroduction: Amyotrophic lateral sclerosis (ALS), a degenerative disorder of the central nervous system, manifests as progressive weakening of muscles. The diagnosis and prognosis of ALS are often unclear, so useful biomarkers are needed. Methods: Total proteins were extracted from muscle samples from 36 ALS, 17 spinal muscular atrophy (SMA), and 36 normal individuals. The expression levels of 134 proteins and phosphoproteins were assessed using protein pathway array analysis. Results: Seventeen proteins were differentially expressed between ALS and normal muscle, and 9 proteins were differentially expressed between ALS and SMA muscle. The low‐level expression of Akt and Factor XIIIB correlates with unfavorable survival, and the risk score calculated based on these proteins predicts the survival of each individual patient. Conclusions: Some proteins could be selected as clinically useful biomarkers. Specifically, Akt and Factor XIIIB were found to be promising biomarkers for estimating prognosis in ALS. Muscle Nerve, 2012
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Neurology 10.1212/01.wnl.0000148648.38313.64
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Published
Sep 19, 2012
Vol/Issue
46(6)
Pages
856-860
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Cite This Article
Fei Yin, Fei Ye, Limei Tan, et al. (2012). Alterations of signaling pathways in muscle tissues of patients with amyotrophic lateral sclerosis. Muscle & Nerve, 46(6), 856-860. https://doi.org/10.1002/mus.23411