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Human Papillomavirus-16 DNA Quantitation Differentiates High-Grade Anal Neoplasia
Background: Due to their higher rates of anal dysplasia/cancer, human immunodeficiency virus (HIV)-positive individuals are recommended to undergo anal dysplasia screening, which consists of anal cytology (AC) and high resolution anoscopy (HRA) with anal biopsy (AB) after abnormal AC result. However...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121871/ https://www.ncbi.nlm.nih.gov/pubmed/30096808 http://dx.doi.org/10.3390/ijerph15081690 |
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author | Agsalda-Garcia, Melissa Shieh, Tiffany Chuang, Eleanore Loi, Nicholas Milne, Cris Fang, Rui Lim, Eunjung Killeen, Jeffrey Shiramizu, Bruce |
author_facet | Agsalda-Garcia, Melissa Shieh, Tiffany Chuang, Eleanore Loi, Nicholas Milne, Cris Fang, Rui Lim, Eunjung Killeen, Jeffrey Shiramizu, Bruce |
author_sort | Agsalda-Garcia, Melissa |
collection | PubMed |
description | Background: Due to their higher rates of anal dysplasia/cancer, human immunodeficiency virus (HIV)-positive individuals are recommended to undergo anal dysplasia screening, which consists of anal cytology (AC) and high resolution anoscopy (HRA) with anal biopsy (AB) after abnormal AC result. However, AC variability limits its usefulness. Our objective was to evaluate human papillomavirus (HPV)-16 DNA quantitation as part of the screening algorithm. Methods: HPV-16 was detected in AC specimens from 75 HIV-positive participants using quantitative real-time polymerase chain reaction. AB results were available from 18/44 patients who had abnormal AC. Statistical tests included Mann-Whitney U, Kruskal-Wallis, receiver operating characteristic (ROC) analysis and Kappa coefficient tests. Results: HPV-16 copy numbers differed significantly across AC (p = 0.001) and AB grades (p = 0.009). HPV-16 ≥ 65 copies/cell predicted high-grade AB (p = 0.04). Using this cut-off in comparison to AB, it had better specificity (1.00) than AC (0.75) and specificity (0.77) than qualitative HPV-16 detection (0.38). Also, the Kappa coefficient of the cut-off (κ = 0.649) was higher than AC (κ = 0.557) and qualitative HPV-16 detection (κ = 0.258) to AB. Conclusion: Higher HPV-16 copy numbers corresponded to higher AC and AB grades, suggesting the importance of HPV burden on disease stage. Furthermore, HPV-16 ≥ 65 copies/cell distinguished high-grade disease and demonstrated better sensitivity, specificity, and agreement with AB than AC or qualitative HPV-16 detection. These results support the potential use of HPV quantitation in conjunction with AC in anal dysplasia screening. |
format | Online Article Text |
id | pubmed-6121871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61218712018-09-07 Human Papillomavirus-16 DNA Quantitation Differentiates High-Grade Anal Neoplasia Agsalda-Garcia, Melissa Shieh, Tiffany Chuang, Eleanore Loi, Nicholas Milne, Cris Fang, Rui Lim, Eunjung Killeen, Jeffrey Shiramizu, Bruce Int J Environ Res Public Health Article Background: Due to their higher rates of anal dysplasia/cancer, human immunodeficiency virus (HIV)-positive individuals are recommended to undergo anal dysplasia screening, which consists of anal cytology (AC) and high resolution anoscopy (HRA) with anal biopsy (AB) after abnormal AC result. However, AC variability limits its usefulness. Our objective was to evaluate human papillomavirus (HPV)-16 DNA quantitation as part of the screening algorithm. Methods: HPV-16 was detected in AC specimens from 75 HIV-positive participants using quantitative real-time polymerase chain reaction. AB results were available from 18/44 patients who had abnormal AC. Statistical tests included Mann-Whitney U, Kruskal-Wallis, receiver operating characteristic (ROC) analysis and Kappa coefficient tests. Results: HPV-16 copy numbers differed significantly across AC (p = 0.001) and AB grades (p = 0.009). HPV-16 ≥ 65 copies/cell predicted high-grade AB (p = 0.04). Using this cut-off in comparison to AB, it had better specificity (1.00) than AC (0.75) and specificity (0.77) than qualitative HPV-16 detection (0.38). Also, the Kappa coefficient of the cut-off (κ = 0.649) was higher than AC (κ = 0.557) and qualitative HPV-16 detection (κ = 0.258) to AB. Conclusion: Higher HPV-16 copy numbers corresponded to higher AC and AB grades, suggesting the importance of HPV burden on disease stage. Furthermore, HPV-16 ≥ 65 copies/cell distinguished high-grade disease and demonstrated better sensitivity, specificity, and agreement with AB than AC or qualitative HPV-16 detection. These results support the potential use of HPV quantitation in conjunction with AC in anal dysplasia screening. MDPI 2018-08-08 2018-08 /pmc/articles/PMC6121871/ /pubmed/30096808 http://dx.doi.org/10.3390/ijerph15081690 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Agsalda-Garcia, Melissa Shieh, Tiffany Chuang, Eleanore Loi, Nicholas Milne, Cris Fang, Rui Lim, Eunjung Killeen, Jeffrey Shiramizu, Bruce Human Papillomavirus-16 DNA Quantitation Differentiates High-Grade Anal Neoplasia |
title | Human Papillomavirus-16 DNA Quantitation Differentiates High-Grade Anal Neoplasia |
title_full | Human Papillomavirus-16 DNA Quantitation Differentiates High-Grade Anal Neoplasia |
title_fullStr | Human Papillomavirus-16 DNA Quantitation Differentiates High-Grade Anal Neoplasia |
title_full_unstemmed | Human Papillomavirus-16 DNA Quantitation Differentiates High-Grade Anal Neoplasia |
title_short | Human Papillomavirus-16 DNA Quantitation Differentiates High-Grade Anal Neoplasia |
title_sort | human papillomavirus-16 dna quantitation differentiates high-grade anal neoplasia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121871/ https://www.ncbi.nlm.nih.gov/pubmed/30096808 http://dx.doi.org/10.3390/ijerph15081690 |
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