Cargando…
Serum S100B Represents a New Biomarker for Mood Disorders
Recently, mood disorders have been discussed to be characterized by glial pathology. The protein S100B, a growth and differentiation factor, is located in, and may actively be released by astro- and oligodendrocytes. This protein is easily assessed in human serum and provides a useful parameter for...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821390/ https://www.ncbi.nlm.nih.gov/pubmed/23701298 http://dx.doi.org/10.2174/13894501113149990014 |
_version_ | 1782290298339065856 |
---|---|
author | Schroeter, Matthias L. Sacher, Julia Steiner, Johann Schoenknecht, Peter Mueller, Karsten |
author_facet | Schroeter, Matthias L. Sacher, Julia Steiner, Johann Schoenknecht, Peter Mueller, Karsten |
author_sort | Schroeter, Matthias L. |
collection | PubMed |
description | Recently, mood disorders have been discussed to be characterized by glial pathology. The protein S100B, a growth and differentiation factor, is located in, and may actively be released by astro- and oligodendrocytes. This protein is easily assessed in human serum and provides a useful parameter for glial activation or injury. Here, we review studies investigating the glial marker S100B in serum of patients with mood disorders. Studies consistently show that S100B is elevated in mood disorders; more strongly in major depressive than bipolar disorder. Consistent with the glial hypothesis of mood disorders, serum S100B levels interact with age with higher levels in elderly depressed subjects. Successful antidepressive treatment has been associated with serum S100B reduction in major depression, whereas there is no evidence of treatment effects in mania. In contrast to the glial marker S100B, the neuronal marker protein neuron-specific enolase is unaltered in mood disorders. Recently, serum S100B has been linked to specific imaging parameters in the human white matter suggesting a role for S100B as an oligodendrocytic marker protein. In sum, serum S100B can be regarded as a promising in vivo biomarker for mood disorders deepening the understanding of the pathogenesis and plasticity-changes in these disorders. Future longitudinal studies combining serum S100B with other cell-specific serum parameters and multimodal imaging are warranted to further explore this serum protein in the development, monitoring and treatment of mood disorders. |
format | Online Article Text |
id | pubmed-3821390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-38213902013-11-11 Serum S100B Represents a New Biomarker for Mood Disorders Schroeter, Matthias L. Sacher, Julia Steiner, Johann Schoenknecht, Peter Mueller, Karsten Curr Drug Targets Article Recently, mood disorders have been discussed to be characterized by glial pathology. The protein S100B, a growth and differentiation factor, is located in, and may actively be released by astro- and oligodendrocytes. This protein is easily assessed in human serum and provides a useful parameter for glial activation or injury. Here, we review studies investigating the glial marker S100B in serum of patients with mood disorders. Studies consistently show that S100B is elevated in mood disorders; more strongly in major depressive than bipolar disorder. Consistent with the glial hypothesis of mood disorders, serum S100B levels interact with age with higher levels in elderly depressed subjects. Successful antidepressive treatment has been associated with serum S100B reduction in major depression, whereas there is no evidence of treatment effects in mania. In contrast to the glial marker S100B, the neuronal marker protein neuron-specific enolase is unaltered in mood disorders. Recently, serum S100B has been linked to specific imaging parameters in the human white matter suggesting a role for S100B as an oligodendrocytic marker protein. In sum, serum S100B can be regarded as a promising in vivo biomarker for mood disorders deepening the understanding of the pathogenesis and plasticity-changes in these disorders. Future longitudinal studies combining serum S100B with other cell-specific serum parameters and multimodal imaging are warranted to further explore this serum protein in the development, monitoring and treatment of mood disorders. Bentham Science Publishers 2013-10 2013-10 /pmc/articles/PMC3821390/ /pubmed/23701298 http://dx.doi.org/10.2174/13894501113149990014 Text en © 2013 Bentham Science Publishers http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Schroeter, Matthias L. Sacher, Julia Steiner, Johann Schoenknecht, Peter Mueller, Karsten Serum S100B Represents a New Biomarker for Mood Disorders |
title | Serum S100B Represents a New Biomarker for Mood Disorders |
title_full | Serum S100B Represents a New Biomarker for Mood Disorders |
title_fullStr | Serum S100B Represents a New Biomarker for Mood Disorders |
title_full_unstemmed | Serum S100B Represents a New Biomarker for Mood Disorders |
title_short | Serum S100B Represents a New Biomarker for Mood Disorders |
title_sort | serum s100b represents a new biomarker for mood disorders |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821390/ https://www.ncbi.nlm.nih.gov/pubmed/23701298 http://dx.doi.org/10.2174/13894501113149990014 |
work_keys_str_mv | AT schroetermatthiasl serums100brepresentsanewbiomarkerformooddisorders AT sacherjulia serums100brepresentsanewbiomarkerformooddisorders AT steinerjohann serums100brepresentsanewbiomarkerformooddisorders AT schoenknechtpeter serums100brepresentsanewbiomarkerformooddisorders AT muellerkarsten serums100brepresentsanewbiomarkerformooddisorders |