Abstract

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.

Highlights

  • Human immunodeficiency virus (HIV)-infected individuals are at a higher risk for developing anal dysplasia and cancer, men who have sex with men (MSM) [1,2,3,4]

  • Histopathological changes in the squamous epithelium of the transitional zone manifest from human papillomavirus (HPV) infection and lead to anal squamous intraepithelial lesions (ASIL) ranging from low-grade to high-grade SIL (LSIL, high-grade squamous intraepithelial lesions (HSIL)) which represents the spectrum of anal dysplasia pathologies including those associated with high-risk HPV types, with HPV-16 accounting for the majority of anal cancer

  • A total of 18 participants completed an high resolution anoscopy (HRA) with anal biopsy (AB) and HPV-16 copy numbers were statistically different according to AB grade (p = 0.009) with the following medians (IQR): Negative 0 (0–117.5), low-grade squamous intraepithelial lesions (LSIL) 3 (0.54–114.5) and HSIL 530 (241–18018), Figure 4

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Summary

Introduction

Human immunodeficiency virus (HIV)-infected individuals are at a higher risk for developing anal dysplasia and cancer, men who have sex with men (MSM) [1,2,3,4]. Histopathological changes in the squamous epithelium of the transitional zone manifest from human papillomavirus (HPV) infection and lead to anal squamous intraepithelial lesions (ASIL) ranging from low-grade to high-grade SIL (LSIL, HSIL) which represents the spectrum of anal dysplasia pathologies including those associated with high-risk HPV types, with HPV-16 accounting for the majority of anal cancer. Res. Public Health 2018, 15, 1690; doi:10.3390/ijerph15081690 www.mdpi.com/journal/ijerph. Public Health 2018, 15, 1690; doi:10.3390/ijerph15081690 www.mdpi.com/journal/ijerph 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. Statistical tests included Mann-Whitney U, Kruskal-Wallis, receiver operating characteristic (ROC)

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