Kinetics of DNA load predict HPV 16 viral clearance

Introduction: While high HPV 16 viral load measured at a single time point is associated with cervical disease outcomes, few studies have assessed changes in HPV 16 viral load on viral clearance. Objective: To measure the association between changes in HPV 16 viral load and viral clearance in a coho...

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Main Authors: M. Marks, P. E. Gravitt, U. Utaipat, S. B. Gupta, K. Liaw, E. Kim, A. Tadesse, C. Phongnarisorn, V. Wootipoom, P. Yuenyao, C. Vipupinyo, S. Rugpao, S. Sriplienchan, D. D. Celentano
Format: Journal
Published: 2018
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Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79953751602&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/50033
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Institution: Chiang Mai University
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Summary:Introduction: While high HPV 16 viral load measured at a single time point is associated with cervical disease outcomes, few studies have assessed changes in HPV 16 viral load on viral clearance. Objective: To measure the association between changes in HPV 16 viral load and viral clearance in a cohort of Thai women infected with HPV 16. Study design: Fifty women (n=50) between the ages of 18-35 years enrolled in a prospective cohort study were followed up every three months for two years. Women positive for HPV 16 DNA by multiplex TaqMan©assay at two or more study visits were selected for viral load quantitation using a type-specific TaqMan©based real-time PCR assay. The strength of the association of change in viral load between two visits and viral clearance at the subsequent visit was assessed using a GEE model for binary outcomes. Results: At study entry, HPV 16 viral load did not vary by infection outcome. A >2. log decline in viral load across two study visits was found to be strongly associated with viral clearance (AOR: 5.5, 95% CI: 1.4-21.3). HPV 16 viral load measured at a single time point was not associated with viral clearance. Conclusions: These results demonstrate that repeated measurement of HPV 16 viral load may be a useful predictor in determining the outcome of early endpoints of viral infection. © 2011 Elsevier B.V.