Triage of human papillomavirus infected women by methylation analysis in first-void urine
Abstract Host cell DNA methylation analysis in urine provides promising triage markers for women diagnosed with a high-risk (HR) human papillomavirus (HPV) infection. In this study, we have investigated a panel of six host cell methylation markers (GHSR, SST, ZIC1, ASCL1, LHX8, ST6GALNAC5) in cervic...
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2021
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oai:doaj.org-article:8720320d3a7b43a68e2ef7b124fc45922021-12-02T14:26:12ZTriage of human papillomavirus infected women by methylation analysis in first-void urine10.1038/s41598-021-87329-12045-2322https://doaj.org/article/8720320d3a7b43a68e2ef7b124fc45922021-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-87329-1https://doaj.org/toc/2045-2322Abstract Host cell DNA methylation analysis in urine provides promising triage markers for women diagnosed with a high-risk (HR) human papillomavirus (HPV) infection. In this study, we have investigated a panel of six host cell methylation markers (GHSR, SST, ZIC1, ASCL1, LHX8, ST6GALNAC5) in cervicovaginal secretions collected within the first part of the urine void (FVU) from a referral population. Cytology, histology, and HPV DNA genotyping results on paired FVU and cervical samples were available. Urinary median methylation levels from HR-HPV (n = 93) positive women were found to increase for all markers with severity of underlying disease. Significantly elevated levels were observed for GHSR and LHX8 in relation to high-grade cervical intraepithelial neoplasia (CIN2 +; n = 33), with area under de curve values of 0.80 (95% Confidence Interval (CI) 0.59–0.92) and 0.76 (95% CI 0.58–0.89), respectively. These findings are the first to support the assertion that methylation analysis of host cell genes is feasible in FVU and holds promise as molecular, triage strategy to discern low- from high-grade cervical disease in HR-HPV positive women. Molecular testing on FVU may serve to increase cervical cancer screening attendance in hard-to-reach populations whilst reducing loss to follow-up and await further optimization and validation studies.Severien Van KeerAnnina P. van SplunterJade PattynAnnemie De SmetSereina A. HerzogXaveer Van OstadeWiebren A. A. TjalmaMargareta IevenPierre Van DammeRenske D. M. SteenbergenAlex VorstersNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-10 (2021) |
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Medicine R Science Q Severien Van Keer Annina P. van Splunter Jade Pattyn Annemie De Smet Sereina A. Herzog Xaveer Van Ostade Wiebren A. A. Tjalma Margareta Ieven Pierre Van Damme Renske D. M. Steenbergen Alex Vorsters Triage of human papillomavirus infected women by methylation analysis in first-void urine |
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Abstract Host cell DNA methylation analysis in urine provides promising triage markers for women diagnosed with a high-risk (HR) human papillomavirus (HPV) infection. In this study, we have investigated a panel of six host cell methylation markers (GHSR, SST, ZIC1, ASCL1, LHX8, ST6GALNAC5) in cervicovaginal secretions collected within the first part of the urine void (FVU) from a referral population. Cytology, histology, and HPV DNA genotyping results on paired FVU and cervical samples were available. Urinary median methylation levels from HR-HPV (n = 93) positive women were found to increase for all markers with severity of underlying disease. Significantly elevated levels were observed for GHSR and LHX8 in relation to high-grade cervical intraepithelial neoplasia (CIN2 +; n = 33), with area under de curve values of 0.80 (95% Confidence Interval (CI) 0.59–0.92) and 0.76 (95% CI 0.58–0.89), respectively. These findings are the first to support the assertion that methylation analysis of host cell genes is feasible in FVU and holds promise as molecular, triage strategy to discern low- from high-grade cervical disease in HR-HPV positive women. Molecular testing on FVU may serve to increase cervical cancer screening attendance in hard-to-reach populations whilst reducing loss to follow-up and await further optimization and validation studies. |
format |
article |
author |
Severien Van Keer Annina P. van Splunter Jade Pattyn Annemie De Smet Sereina A. Herzog Xaveer Van Ostade Wiebren A. A. Tjalma Margareta Ieven Pierre Van Damme Renske D. M. Steenbergen Alex Vorsters |
author_facet |
Severien Van Keer Annina P. van Splunter Jade Pattyn Annemie De Smet Sereina A. Herzog Xaveer Van Ostade Wiebren A. A. Tjalma Margareta Ieven Pierre Van Damme Renske D. M. Steenbergen Alex Vorsters |
author_sort |
Severien Van Keer |
title |
Triage of human papillomavirus infected women by methylation analysis in first-void urine |
title_short |
Triage of human papillomavirus infected women by methylation analysis in first-void urine |
title_full |
Triage of human papillomavirus infected women by methylation analysis in first-void urine |
title_fullStr |
Triage of human papillomavirus infected women by methylation analysis in first-void urine |
title_full_unstemmed |
Triage of human papillomavirus infected women by methylation analysis in first-void urine |
title_sort |
triage of human papillomavirus infected women by methylation analysis in first-void urine |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/8720320d3a7b43a68e2ef7b124fc4592 |
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