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Development of biomarkers for multiple sclerosis as a neurodegenerative disorder

期刊

PROGRESS IN NEUROBIOLOGY
卷 95, 期 4, 页码 670-685

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pneurobio.2011.04.007

关键词

Multiple sclerosis; Biomarkers; Neurodegeneration

资金

  1. LOEWE Neuronal Coordination Research Focus Frankfurt (NeFF)
  2. Merck Inc., USA
  3. Biogen Idec
  4. TEVA
  5. Merck Serono
  6. Deutsche Forschungsgemeinschaft
  7. Bayer Schering
  8. Genzyme-Virotec
  9. Merck-Serono
  10. Novartis
  11. Roche
  12. TEVA Pharma
  13. Gemeinnutzige Hertie-Stiftung
  14. GBS-Polyradiculitis-Stiftung
  15. University of Ulm
  16. Landesstiftung BW

向作者/读者索取更多资源

Multiple sclerosis (MS) is the most common neurological disorder leading to permanent disability in young adults in the developed world. While traditionally conceived as an autoimmune inflammatory disease it is becoming increasingly evident that axonal and neuronal degeneration occur, at least partly independent of inflammation, and already at the earliest stages of the disease. In addition, it is the progressive neurodegeneration which determines the amount of accumulating clinical disability. Therefore, MS should be considered as a neurodegenerative disorder. Development of disease-modifying drugs to treat MS is currently highly dynamic. Already, several drugs have shown short-term efficacy to delay progression of clinical disability, but the ultimate aim is to halt disease progression. In this context, the development of sensitive, reliable and valid biomarkers to measure neurodegeneration is an indispensible need to facilitate successful informative clinical trials. While no such biomarker is currently fully established, several promising candidate biomarkers obtained with multimodal techniques, including cerebrospinal fluid and serum analysis, neuroimaging and neurophysiology, are presently developed and evaluated. This paper compiles an up-to-date critical review of the available knowledge of candidate biomarkers of neurodegenerative processes in MS. (C) 2011 Elsevier Ltd. All rights reserved.

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