Prospective investigation of polyomavirus infection and the risk of adult glioma

Abstract 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...

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Autores principales: Kathleen M. Egan, Youngchul Kim, Noemi Bender, James M. Hodge, Anna E. Coghill, Stephanie A. Smith-Warner, Dana E. Rollison, Lauren R. Teras, Tom K. Grimsrud, Tim Waterboer
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/c7e69f91592248d6ac0f7c5a0a840ccf
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spelling oai:doaj.org-article:c7e69f91592248d6ac0f7c5a0a840ccf2021-12-02T14:29:03ZProspective investigation of polyomavirus infection and the risk of adult glioma10.1038/s41598-021-89133-32045-2322https://doaj.org/article/c7e69f91592248d6ac0f7c5a0a840ccf2021-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-89133-3https://doaj.org/toc/2045-2322Abstract 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.Kathleen M. EganYoungchul KimNoemi BenderJames M. HodgeAnna E. CoghillStephanie A. Smith-WarnerDana E. RollisonLauren R. TerasTom K. GrimsrudTim WaterboerNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Kathleen M. Egan
Youngchul Kim
Noemi Bender
James M. Hodge
Anna E. Coghill
Stephanie A. Smith-Warner
Dana E. Rollison
Lauren R. Teras
Tom K. Grimsrud
Tim Waterboer
Prospective investigation of polyomavirus infection and the risk of adult glioma
description Abstract 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 article
author Kathleen M. Egan
Youngchul Kim
Noemi Bender
James M. Hodge
Anna E. Coghill
Stephanie A. Smith-Warner
Dana E. Rollison
Lauren R. Teras
Tom K. Grimsrud
Tim Waterboer
author_facet Kathleen M. Egan
Youngchul Kim
Noemi Bender
James M. Hodge
Anna E. Coghill
Stephanie A. Smith-Warner
Dana E. Rollison
Lauren R. Teras
Tom K. Grimsrud
Tim Waterboer
author_sort Kathleen M. Egan
title 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_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_sort prospective investigation of polyomavirus infection and the risk of adult glioma
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/c7e69f91592248d6ac0f7c5a0a840ccf
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