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Human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples
The performance and acceptability of first-void urine as specimen for the detection of HPV DNA in a Belgian referral population was evaluated using an optimized sample collection and processing protocol. One hundred ten first-void urine and cervical samples were collected from 25- to 64-year-old wom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916996/ https://www.ncbi.nlm.nih.gov/pubmed/29417310 http://dx.doi.org/10.1007/s10096-017-3179-1 |
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author | Van Keer, Severien Tjalma, Wiebren A. A. Pattyn, Jade Biesmans, Samantha Pieters, Zoë Van Ostade, Xaveer Ieven, Margareta Van Damme, Pierre Vorsters, Alex |
author_facet | Van Keer, Severien Tjalma, Wiebren A. A. Pattyn, Jade Biesmans, Samantha Pieters, Zoë Van Ostade, Xaveer Ieven, Margareta Van Damme, Pierre Vorsters, Alex |
author_sort | Van Keer, Severien |
collection | PubMed |
description | The performance and acceptability of first-void urine as specimen for the detection of HPV DNA in a Belgian referral population was evaluated using an optimized sample collection and processing protocol. One hundred ten first-void urine and cervical samples were collected from 25- to 64-year-old women who were referred for colposcopy (January–November 2016). Paired samples were analyzed by the Riatol qPCR HPV genotyping assay. Acceptability data were gathered through questionnaires (NCT02714127). A higher high-risk HPV DNA prevalence was observed in first-void urine (n = 76/110) compared to cervical samples (n = 73/110), with HPV31 and HPV16/31 being most prevalent correspondingly. For both any and high-risk HPV DNA, good agreement was observed between paired samples (Cohen’s Kappa of 0.660 (95% CI: 0.486–0.833) and 0.688 (95% CI: 0.542–0.835), respectively). In addition, significant positive correlations in HPV copies (per microliter of DNA extract) between paired samples were observed for HPV16 (r(s) = 0.670; FDR (false discovery rate)-adjusted p = 0.006), HPV18 (r(s) = 0.893; FDR-adjusted p = 0.031), HPV31 (r(s) = 0.527; FDR-adjusted p = 0.031), HPV53 (r(s) = 0.691; FDR-adjusted p = 0.017), and HPV68 (r(s) = 0.569; FDR-adjusted p = 0.031). First-void urine sampling using a first-void urine collection device was preferred over a clinician-collected cervical sample. And mostly, first-void urine sampling at home was favored over collection at the clinic or the general practitioner’s office. First-void urine sampling is a highly preferred, non-invasive method that ensures good agreement in HPV DNA (copies) with reference cervical samples. It is particularly interesting as a screening technique to reach non-participants, and its clinical performance should be further evaluated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10096-017-3179-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5916996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-59169962018-04-30 Human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples Van Keer, Severien Tjalma, Wiebren A. A. Pattyn, Jade Biesmans, Samantha Pieters, Zoë Van Ostade, Xaveer Ieven, Margareta Van Damme, Pierre Vorsters, Alex Eur J Clin Microbiol Infect Dis Original Article The performance and acceptability of first-void urine as specimen for the detection of HPV DNA in a Belgian referral population was evaluated using an optimized sample collection and processing protocol. One hundred ten first-void urine and cervical samples were collected from 25- to 64-year-old women who were referred for colposcopy (January–November 2016). Paired samples were analyzed by the Riatol qPCR HPV genotyping assay. Acceptability data were gathered through questionnaires (NCT02714127). A higher high-risk HPV DNA prevalence was observed in first-void urine (n = 76/110) compared to cervical samples (n = 73/110), with HPV31 and HPV16/31 being most prevalent correspondingly. For both any and high-risk HPV DNA, good agreement was observed between paired samples (Cohen’s Kappa of 0.660 (95% CI: 0.486–0.833) and 0.688 (95% CI: 0.542–0.835), respectively). In addition, significant positive correlations in HPV copies (per microliter of DNA extract) between paired samples were observed for HPV16 (r(s) = 0.670; FDR (false discovery rate)-adjusted p = 0.006), HPV18 (r(s) = 0.893; FDR-adjusted p = 0.031), HPV31 (r(s) = 0.527; FDR-adjusted p = 0.031), HPV53 (r(s) = 0.691; FDR-adjusted p = 0.017), and HPV68 (r(s) = 0.569; FDR-adjusted p = 0.031). First-void urine sampling using a first-void urine collection device was preferred over a clinician-collected cervical sample. And mostly, first-void urine sampling at home was favored over collection at the clinic or the general practitioner’s office. First-void urine sampling is a highly preferred, non-invasive method that ensures good agreement in HPV DNA (copies) with reference cervical samples. It is particularly interesting as a screening technique to reach non-participants, and its clinical performance should be further evaluated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10096-017-3179-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-02-07 2018 /pmc/articles/PMC5916996/ /pubmed/29417310 http://dx.doi.org/10.1007/s10096-017-3179-1 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Van Keer, Severien Tjalma, Wiebren A. A. Pattyn, Jade Biesmans, Samantha Pieters, Zoë Van Ostade, Xaveer Ieven, Margareta Van Damme, Pierre Vorsters, Alex Human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples |
title | Human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples |
title_full | Human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples |
title_fullStr | Human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples |
title_full_unstemmed | Human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples |
title_short | Human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples |
title_sort | human papillomavirus genotype and viral load agreement between paired first-void urine and clinician-collected cervical samples |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916996/ https://www.ncbi.nlm.nih.gov/pubmed/29417310 http://dx.doi.org/10.1007/s10096-017-3179-1 |
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