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DC Field | Value | Language |
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dc.contributor.author | M. Marks | en_US |
dc.contributor.author | P. E. Gravitt | en_US |
dc.contributor.author | U. Utaipat | en_US |
dc.contributor.author | S. B. Gupta | en_US |
dc.contributor.author | K. Liaw | en_US |
dc.contributor.author | E. Kim | en_US |
dc.contributor.author | A. Tadesse | en_US |
dc.contributor.author | C. Phongnarisorn | en_US |
dc.contributor.author | V. Wootipoom | en_US |
dc.contributor.author | P. Yuenyao | en_US |
dc.contributor.author | C. Vipupinyo | en_US |
dc.contributor.author | S. Rugpao | en_US |
dc.contributor.author | S. Sriplienchan | en_US |
dc.contributor.author | D. D. Celentano | en_US |
dc.date.accessioned | 2018-09-04T04:22:20Z | - |
dc.date.available | 2018-09-04T04:22:20Z | - |
dc.date.issued | 2011-05-01 | en_US |
dc.identifier.issn | 13866532 | en_US |
dc.identifier.other | 2-s2.0-79953751602 | en_US |
dc.identifier.other | 10.1016/j.jcv.2011.01.011 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79953751602&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/50033 | - |
dc.description.abstract | 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. | en_US |
dc.subject | Immunology and Microbiology | en_US |
dc.subject | Medicine | en_US |
dc.title | Kinetics of DNA load predict HPV 16 viral clearance | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Journal of Clinical Virology | en_US |
article.volume | 51 | en_US |
article.stream.affiliations | Johns Hopkins Bloomberg School of Public Health | en_US |
article.stream.affiliations | Merck & Co., Inc. | en_US |
article.stream.affiliations | Merck Research Laboratories | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Prince of Songkla University | en_US |
article.stream.affiliations | Khon Kaen University | en_US |
article.stream.affiliations | Rajavithi Hospital | en_US |
article.stream.affiliations | Research Institute for Health Sciences | en_US |
Appears in Collections: | CMUL: Journal Articles |
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