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Prospective investigation of polyomavirus infection and the risk of adult glioma
Glioma is an aggressive primary tumor of the brain with a poorly understood etiology. We studied the association of 4 human polyomaviruses (HPyV)—JC virus (JCV), BK virus (BKV), human polyomavirus 6 (HPyV6), and Merkel cell polyomavirus (MCPyV) with glioma risk within the Cancer Prevention Study II...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100283/ https://www.ncbi.nlm.nih.gov/pubmed/33953301 http://dx.doi.org/10.1038/s41598-021-89133-3 |
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author | Egan, Kathleen M. Kim, Youngchul Bender, Noemi Hodge, James M. Coghill, Anna E. Smith-Warner, Stephanie A. Rollison, Dana E. Teras, Lauren R. Grimsrud, Tom K. Waterboer, Tim |
author_facet | Egan, Kathleen M. Kim, Youngchul Bender, Noemi Hodge, James M. Coghill, Anna E. Smith-Warner, Stephanie A. Rollison, Dana E. Teras, Lauren R. Grimsrud, Tom K. Waterboer, Tim |
author_sort | Egan, Kathleen M. |
collection | PubMed |
description | Glioma is an aggressive primary tumor of the brain with a poorly understood etiology. We studied the association of 4 human polyomaviruses (HPyV)—JC virus (JCV), BK virus (BKV), human polyomavirus 6 (HPyV6), and Merkel cell polyomavirus (MCPyV) with glioma risk within the Cancer Prevention Study II in the US (CPS-II) and the Janus Serum Bank in Norway. Cohort participants subsequently diagnosed with glioma from the CPS-II (n = 37) and Janus Serum Bank (n = 323), a median of 6.9 and 15.4 years after blood collection, respectively, were matched to individual controls on age, sex, and date of blood draw. Serum antibodies to the major viral capsid protein (VP1) were used to establish infection history for each polyomavirus. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using conditional logistic regression. In the Janus Serum Bank, MCPyV infection was associated with a higher risk of glioma overall (OR: 1.56; 95% CI 1.10, 2.19). A modest, nonsignificant positive association with MCPyV infection was also observed in CPS-II (OR: 1.29; 95% CI 0.54, 3.08). In both cohorts, glioma risk was not significantly related to infection with JCV, BKV or HPyV6. The present study suggests that MCPyV infection may increase glioma risk. |
format | Online Article Text |
id | pubmed-8100283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81002832021-05-07 Prospective investigation of polyomavirus infection and the risk of adult glioma Egan, Kathleen M. Kim, Youngchul Bender, Noemi Hodge, James M. Coghill, Anna E. Smith-Warner, Stephanie A. Rollison, Dana E. Teras, Lauren R. Grimsrud, Tom K. Waterboer, Tim Sci Rep Article Glioma is an aggressive primary tumor of the brain with a poorly understood etiology. We studied the association of 4 human polyomaviruses (HPyV)—JC virus (JCV), BK virus (BKV), human polyomavirus 6 (HPyV6), and Merkel cell polyomavirus (MCPyV) with glioma risk within the Cancer Prevention Study II in the US (CPS-II) and the Janus Serum Bank in Norway. Cohort participants subsequently diagnosed with glioma from the CPS-II (n = 37) and Janus Serum Bank (n = 323), a median of 6.9 and 15.4 years after blood collection, respectively, were matched to individual controls on age, sex, and date of blood draw. Serum antibodies to the major viral capsid protein (VP1) were used to establish infection history for each polyomavirus. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using conditional logistic regression. In the Janus Serum Bank, MCPyV infection was associated with a higher risk of glioma overall (OR: 1.56; 95% CI 1.10, 2.19). A modest, nonsignificant positive association with MCPyV infection was also observed in CPS-II (OR: 1.29; 95% CI 0.54, 3.08). In both cohorts, glioma risk was not significantly related to infection with JCV, BKV or HPyV6. The present study suggests that MCPyV infection may increase glioma risk. Nature Publishing Group UK 2021-05-05 /pmc/articles/PMC8100283/ /pubmed/33953301 http://dx.doi.org/10.1038/s41598-021-89133-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Egan, Kathleen M. Kim, Youngchul Bender, Noemi Hodge, James M. Coghill, Anna E. Smith-Warner, Stephanie A. Rollison, Dana E. Teras, Lauren R. Grimsrud, Tom K. Waterboer, Tim Prospective investigation of polyomavirus infection and the risk of adult glioma |
title | Prospective investigation of polyomavirus infection and the risk of adult glioma |
title_full | Prospective investigation of polyomavirus infection and the risk of adult glioma |
title_fullStr | Prospective investigation of polyomavirus infection and the risk of adult glioma |
title_full_unstemmed | Prospective investigation of polyomavirus infection and the risk of adult glioma |
title_short | Prospective investigation of polyomavirus infection and the risk of adult glioma |
title_sort | prospective investigation of polyomavirus infection and the risk of adult glioma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100283/ https://www.ncbi.nlm.nih.gov/pubmed/33953301 http://dx.doi.org/10.1038/s41598-021-89133-3 |
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