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Plasma Levels of S100B in Preeclampsia and Association With Possible Central Nervous System Effects
BACKGROUND: S100B is supposed to be a peripheral biomarker of central nervous system (CNS) injury. The purpose of this study was to compare levels of S100B in women with preeclampsia with levels in healthy pregnant control subjects and furthermore to analyze levels of S100B in relation to possible C...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4125339/ https://www.ncbi.nlm.nih.gov/pubmed/24610883 http://dx.doi.org/10.1093/ajh/hpu020 |
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author | Bergman, Lina Akhter, Tansim Wikström, Anna-Karin Wikström, Johan Naessen, Tord Åkerud, Helena |
author_facet | Bergman, Lina Akhter, Tansim Wikström, Anna-Karin Wikström, Johan Naessen, Tord Åkerud, Helena |
author_sort | Bergman, Lina |
collection | PubMed |
description | BACKGROUND: S100B is supposed to be a peripheral biomarker of central nervous system (CNS) injury. The purpose of this study was to compare levels of S100B in women with preeclampsia with levels in healthy pregnant control subjects and furthermore to analyze levels of S100B in relation to possible CNS effects. METHODS: A cross-sectional case–control study in antenatal care centers in Uppsala, Sweden, was performed. Fifty-three women with preeclampsia and 58 healthy pregnant women were recruited at similar gestational length; women with preeclampsia were recruited at time of diagnosis, and control subjects were recruited during their routine visit to an antenatal clinic. Plasma samples were collected, and levels of S100B were analyzed with an enzyme-linked immunosorbent assay. Information about demographic and clinical characteristics, including symptoms related to CNS affection, was collected from the medical records. The main outcome measures were plasma levels of S100B and possible CNS effects. RESULTS: Levels of S100B were significantly higher among women with preeclampsia than among control subjects (0.12 µg/L vs. 0.07 µg/L; P < 0.001). In preeclampsia, there was a significant association between high levels of S100B and visual disturbances (P < 0.05). CONCLUSIONS: S100B is increased among women with preeclampsia, and high levels of S100B associate with visual disturbances, which might reflect CNS affection in women with preeclampsia. |
format | Online Article Text |
id | pubmed-4125339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41253392015-08-01 Plasma Levels of S100B in Preeclampsia and Association With Possible Central Nervous System Effects Bergman, Lina Akhter, Tansim Wikström, Anna-Karin Wikström, Johan Naessen, Tord Åkerud, Helena Am J Hypertens Original Article BACKGROUND: S100B is supposed to be a peripheral biomarker of central nervous system (CNS) injury. The purpose of this study was to compare levels of S100B in women with preeclampsia with levels in healthy pregnant control subjects and furthermore to analyze levels of S100B in relation to possible CNS effects. METHODS: A cross-sectional case–control study in antenatal care centers in Uppsala, Sweden, was performed. Fifty-three women with preeclampsia and 58 healthy pregnant women were recruited at similar gestational length; women with preeclampsia were recruited at time of diagnosis, and control subjects were recruited during their routine visit to an antenatal clinic. Plasma samples were collected, and levels of S100B were analyzed with an enzyme-linked immunosorbent assay. Information about demographic and clinical characteristics, including symptoms related to CNS affection, was collected from the medical records. The main outcome measures were plasma levels of S100B and possible CNS effects. RESULTS: Levels of S100B were significantly higher among women with preeclampsia than among control subjects (0.12 µg/L vs. 0.07 µg/L; P < 0.001). In preeclampsia, there was a significant association between high levels of S100B and visual disturbances (P < 0.05). CONCLUSIONS: S100B is increased among women with preeclampsia, and high levels of S100B associate with visual disturbances, which might reflect CNS affection in women with preeclampsia. Oxford University Press 2014-08 2014-03-07 /pmc/articles/PMC4125339/ /pubmed/24610883 http://dx.doi.org/10.1093/ajh/hpu020 Text en © The Author 2014. Published by Oxford University Press on behalf of the American Journal of Hypertension. http://creativecommons.org/licenses/by-nc-nd/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Bergman, Lina Akhter, Tansim Wikström, Anna-Karin Wikström, Johan Naessen, Tord Åkerud, Helena Plasma Levels of S100B in Preeclampsia and Association With Possible Central Nervous System Effects |
title | Plasma Levels of S100B in Preeclampsia and Association With Possible Central Nervous System Effects |
title_full | Plasma Levels of S100B in Preeclampsia and Association With Possible Central Nervous System Effects |
title_fullStr | Plasma Levels of S100B in Preeclampsia and Association With Possible Central Nervous System Effects |
title_full_unstemmed | Plasma Levels of S100B in Preeclampsia and Association With Possible Central Nervous System Effects |
title_short | Plasma Levels of S100B in Preeclampsia and Association With Possible Central Nervous System Effects |
title_sort | plasma levels of s100b in preeclampsia and association with possible central nervous system effects |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4125339/ https://www.ncbi.nlm.nih.gov/pubmed/24610883 http://dx.doi.org/10.1093/ajh/hpu020 |
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