Literature DB >> 17187827

Plasma S100beta and NSE levels and progression in multiple sclerosis.

Marcus Koch1, Jop Mostert, Dorothea Heersema, Albert Teelken, Jacques De Keyser.   

Abstract

Plasma levels of the glial cell marker S100beta and the neuronal marker neuron-specific enolase (NSE) are elevated in various conditions of central nervous system damage. In this study we investigated whether plasma levels of S100beta and NSE are related to disease progression in multiple sclerosis (MS). Plasma levels of S100beta and NSE were measured in 25 patients with relapsing remitting MS (RRMS), 23 with secondary progressive MS (SPMS) and 16 with primary progressive MS (PPMS). All MS patients were in a clinically stable phase. Progression and disability were evaluated during a follow-up period of five years. We found that plasma NSE levels were lower in patients with clinically relevant worsening on the Expanded Disability Status Scale (EDSS), defined as 1 point increase from EDSS <6.0 or 0.5 point increase from EDSS> or =6 after five years (p=0.042), and in patients with a progressive disease course (p=0.01). There was a significant negative correlation between plasma NSE levels and both EDSS and Multiple Sclerosis Severity Status (MSSS) scores at baseline and after five years of follow-up (r=-0.33 and -0.38, p=0.027 and 0.003). There were no significant differences between patient groups in plasma S100beta levels. Plasma NSE levels appear inversely related to disease progression in MS.

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Year:  2006        PMID: 17187827     DOI: 10.1016/j.jns.2006.11.012

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


  10 in total

Review 1.  White-matter astrocytes, axonal energy metabolism, and axonal degeneration in multiple sclerosis.

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2.  Serum neuron specific enolase may be a marker to predict the severity and outcome of cerebral venous thrombosis.

Authors:  Yanyu Hu; Ran Meng; Xuxiang Zhang; Linlin Guo; Sijie Li; Yan Wu; Jiangang Duan; Yuchuan Ding; Xunming Ji
Journal:  J Neurol       Date:  2017-11-11       Impact factor: 4.849

3.  Enolase and arrestin are novel nonmyelin autoantigens in multiple sclerosis.

Authors:  Farzin Forooghian; Roy K Cheung; W Clay Smith; Paul O'Connor; Hans-Michael Dosch
Journal:  J Clin Immunol       Date:  2007-04-10       Impact factor: 8.317

Review 4.  Current and Future Biomarkers in Multiple Sclerosis.

Authors:  Jennifer Yang; Maysa Hamade; Qi Wu; Qin Wang; Robert Axtell; Shailendra Giri; Yang Mao-Draayer
Journal:  Int J Mol Sci       Date:  2022-05-24       Impact factor: 6.208

5.  S100 protein family and its application in clinical practice.

Authors:  F Sedaghat; A Notopoulos
Journal:  Hippokratia       Date:  2008       Impact factor: 0.471

6.  Cerebrospinal fluid and blood biomarkers of neuroaxonal damage in multiple sclerosis.

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Journal:  Mult Scler Int       Date:  2011-05-02

7.  Plasma neuronal specific enolase: a potential stage diagnostic marker in human African trypanosomiasis.

Authors:  Jeremy M Sternberg; Julia A Mitchell
Journal:  Trans R Soc Trop Med Hyg       Date:  2014-04-30       Impact factor: 2.184

Review 8.  New Insights into the Role of Neuron-Specific Enolase in Neuro-Inflammation, Neurodegeneration, and Neuroprotection.

Authors:  Azizul Haque; Rachel Polcyn; Denise Matzelle; Naren L Banik
Journal:  Brain Sci       Date:  2018-02-18

Review 9.  Biomarkers in Neuropsychiatric Systemic Lupus Erythematosus: A Systematic Literature Review of the Last Decade.

Authors:  Julius Lindblom; Chandra Mohan; Ioannis Parodis
Journal:  Brain Sci       Date:  2022-01-30

10.  Can we distinguish stroke and stroke mimics via red cell distribution width in young patients?

Authors:  Recep Demir; Murat Saritemur; Omer Atis; Lutfi Ozel; İdris Kocaturk; Mucahit Emet; Hizir Ulvi
Journal:  Arch Med Sci       Date:  2015-10-12       Impact factor: 3.318

  10 in total

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