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Human immunoglobulin G levels of viruses and associated glioma risk
Few consistent etiological factors have been identified for primary brain tumors. Inverse associations to asthma and low levels of varicella-zoster virus, immunoglobulin (Ig) levels in prevalent cases have indicted a role for the immune system in the development of glioma. Because samples from preva...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146711/ https://www.ncbi.nlm.nih.gov/pubmed/21717196 http://dx.doi.org/10.1007/s10552-011-9799-3 |
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author | Sjöström, Sara Hjalmars, Ulf Juto, Per Wadell, Göran Hallmans, Göran Tjönneland, Anne Halkjaer, Jytte Manjer, Jonas Almquist, Martin Melin, Beatrice S. |
author_facet | Sjöström, Sara Hjalmars, Ulf Juto, Per Wadell, Göran Hallmans, Göran Tjönneland, Anne Halkjaer, Jytte Manjer, Jonas Almquist, Martin Melin, Beatrice S. |
author_sort | Sjöström, Sara |
collection | PubMed |
description | Few consistent etiological factors have been identified for primary brain tumors. Inverse associations to asthma and low levels of varicella-zoster virus, immunoglobulin (Ig) levels in prevalent cases have indicted a role for the immune system in the development of glioma. Because samples from prevalent cases of glioma could be influenced by treatments such as steroids and chemotherapy, we investigated pre-diagnostic samples from three large Scandinavian cohorts. To test the hypothesis that immune response levels to these viruses are associated etiologically with glioma risk, we investigated pre-diagnostic immunoglobulin levels for cytomegalovirus (CMV), varicella-zoster virus (VZV), adenovirus (Ad), and Epstein-Barr virus (EBV) including the nuclear antigen (EBNA1) using plasma samples from 197 cases of adult glioma and 394 controls collected from population-based cohorts in Sweden and Denmark. Low VZV IgG levels were marginally significantly more common in glioma cases than the controls (odds ratio (OR) = 0.68, 95% CI 0.41–1.13) for the fourth compared with the first quartile (p = 0.06 for trend). These results were more prominent when analyzing cases with blood sampling at least 2 years before diagnosis (OR = 0.63, 95% CI 0.37–1.08) (p = 0.03). No association with glioma risk was observed for CMV, EBV, and adenovirus. |
format | Online Article Text |
id | pubmed-3146711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-31467112011-09-08 Human immunoglobulin G levels of viruses and associated glioma risk Sjöström, Sara Hjalmars, Ulf Juto, Per Wadell, Göran Hallmans, Göran Tjönneland, Anne Halkjaer, Jytte Manjer, Jonas Almquist, Martin Melin, Beatrice S. Cancer Causes Control Article Few consistent etiological factors have been identified for primary brain tumors. Inverse associations to asthma and low levels of varicella-zoster virus, immunoglobulin (Ig) levels in prevalent cases have indicted a role for the immune system in the development of glioma. Because samples from prevalent cases of glioma could be influenced by treatments such as steroids and chemotherapy, we investigated pre-diagnostic samples from three large Scandinavian cohorts. To test the hypothesis that immune response levels to these viruses are associated etiologically with glioma risk, we investigated pre-diagnostic immunoglobulin levels for cytomegalovirus (CMV), varicella-zoster virus (VZV), adenovirus (Ad), and Epstein-Barr virus (EBV) including the nuclear antigen (EBNA1) using plasma samples from 197 cases of adult glioma and 394 controls collected from population-based cohorts in Sweden and Denmark. Low VZV IgG levels were marginally significantly more common in glioma cases than the controls (odds ratio (OR) = 0.68, 95% CI 0.41–1.13) for the fourth compared with the first quartile (p = 0.06 for trend). These results were more prominent when analyzing cases with blood sampling at least 2 years before diagnosis (OR = 0.63, 95% CI 0.37–1.08) (p = 0.03). No association with glioma risk was observed for CMV, EBV, and adenovirus. Springer Netherlands 2011-06-30 2011 /pmc/articles/PMC3146711/ /pubmed/21717196 http://dx.doi.org/10.1007/s10552-011-9799-3 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Article Sjöström, Sara Hjalmars, Ulf Juto, Per Wadell, Göran Hallmans, Göran Tjönneland, Anne Halkjaer, Jytte Manjer, Jonas Almquist, Martin Melin, Beatrice S. Human immunoglobulin G levels of viruses and associated glioma risk |
title | Human immunoglobulin G levels of viruses and associated glioma risk |
title_full | Human immunoglobulin G levels of viruses and associated glioma risk |
title_fullStr | Human immunoglobulin G levels of viruses and associated glioma risk |
title_full_unstemmed | Human immunoglobulin G levels of viruses and associated glioma risk |
title_short | Human immunoglobulin G levels of viruses and associated glioma risk |
title_sort | human immunoglobulin g levels of viruses and associated glioma risk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146711/ https://www.ncbi.nlm.nih.gov/pubmed/21717196 http://dx.doi.org/10.1007/s10552-011-9799-3 |
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