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Type-dependent association between risk of cervical intraepithelial neoplasia and viral load of oncogenic human papillomavirus types other than types 16 and 18.
Fu Xi, Long; Schiffman, Mark; Ke, Yang; Hughes, James P; Galloway, Denise A; He, Zhonghu; Hulbert, Ayaka; Winer, Rachel L; Koutsky, Laura A; Kiviat, Nancy B.
Afiliação
  • Fu Xi L; Department of Pathology, School of Medicine, University of Washington, Seattle, WA.
  • Schiffman M; Department of Epidemiology, University of Washington, Seattle, WA.
  • Ke Y; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD.
  • Hughes JP; Key Laboratory of Carcinogenesis and Translational Research, Peking University School of Oncology, Beijing, People's Republic of China.
  • Galloway DA; Department of Biostatistics, School of Public Health and Community Medicine, University of Washington, Seattle, WA.
  • He Z; Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Hulbert A; Key Laboratory of Carcinogenesis and Translational Research, Peking University School of Oncology, Beijing, People's Republic of China.
  • Winer RL; Department of Pathology, School of Medicine, University of Washington, Seattle, WA.
  • Koutsky LA; Department of Epidemiology, University of Washington, Seattle, WA.
  • Kiviat NB; Department of Epidemiology, University of Washington, Seattle, WA.
Int J Cancer ; 140(8): 1747-1756, 2017 04 15.
Article em En | MEDLINE | ID: mdl-28052328
ABSTRACT
Studies of the clinical relevance of human papillomavirus (HPV) DNA load have focused mainly on HPV16 and HPV18. Data on other oncogenic types are rare. Study subjects were women enrolled in the atypical squamous cells of undetermined significance (ASC-US) and low-grade squamous intraepithelial lesion (LSIL) triage study who had ≥1 of 11 non-HPV16/18 oncogenic types detected during a 2-year follow-up at 6-month intervals. Viral load measurements were performed on the first type-specific HPV-positive specimens. The association of cervical intraepithelial neoplasia grades 2-3 (CIN2/3) with type-specific HPV DNA load was assessed with discrete-time Cox regression. Overall, the increase in the cumulative risk of CIN2/3 per 1 unit increase in log10 -transformed viral load was statistically significant for four types within species 9 including HPV31 (adjusted hazard ratio [HR adjusted ] = 1.32 95% confidence interval [CI], 1.14-1.52), HPV35 (HR adjusted = 1.47; 95% CI, 1.23-1.76), HPV52 (HR adjusted = 1.14; 95% CI, 1.01-1.30) and HPV58 (HR adjusted = 1.49; 95% CI, 1.23-1.82). The association was marginally significant for HPV33 (species 9) and HPV45 (species 7) and was not appreciable for other types. The per 1 log10 -unit increase in viral load of a group of species 9 non-HPV16 oncogenic types was statistically significantly associated with risk of CIN2/3 for women with a cytologic diagnosis of within normal limits, ASC-US, or LSIL at the first HPV-positive visit but not for those with high-grade SIL. Findings suggest that the viral load-associated risk of CIN2/3 is type-dependent, and mainly restricted to the species of HPV types related to HPV16, which shares this association.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Papillomaviridae / DNA Viral / Displasia do Colo do Útero / Infecções por Papillomavirus Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Papillomaviridae / DNA Viral / Displasia do Colo do Útero / Infecções por Papillomavirus Idioma: En Ano de publicação: 2017 Tipo de documento: Article