A cross-sectional study of high-risk human papillomavirus clustering and cervical outcomes in HIV-infected women in Rio de Janeiro, Brazil
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | CASTILHO, Jessica L. | |
dc.contributor.author | LEVI, Jose Eduardo | |
dc.contributor.author | LUZ, Paula M. | |
dc.contributor.author | CAMBOU, Mary Catherine | |
dc.contributor.author | VANNI, Tazio | |
dc.contributor.author | ANDRADE, Angela de | |
dc.contributor.author | DERRICO, Monica | |
dc.contributor.author | VELOSO, Valdilea G. | |
dc.contributor.author | GRINSZTEJN, Beatriz | |
dc.contributor.author | FRIEDMAN, Ruth K. | |
dc.date.accessioned | 2015-10-26T16:50:11Z | |
dc.date.available | 2015-10-26T16:50:11Z | |
dc.date.issued | 2015 | |
dc.description.abstract | Background: In Brazil, the rate of cervical cancer remains high despite the availability of screening programs. With ongoing vaccine development and implementation, information on the prevalence of specific HPV types is needed, particularly among high-risk populations, such as HIV-infected women. Methods: We performed a study of HIV-infected women in Rio de Janeiro, Brazil, who underwent cervical HPV genotype testing between 2005-2013. We examined the prevalence of high-risk HPV types and the patterns of high-risk HPV type clustering. Using logarithmic binomial regression, we estimated the risk of abnormal cytology by HPV genotype result. Results: Of the 562 women included, 498 (89 %) had at least one HPV type detected. 364 women (65 %) had at least one high-risk HPV type detected and 181 (32 %) had more than one high-risk type detected. HPV 58 was the most frequent HPV type detected overall (prevalence 19.8 % [95 % confidence interval 16.4-23.1]), followed by HPV 53 (prevalence 15.5 % [12.5-18.5]) and HPV 16 (prevalence 13 % [10.2-15.8]). Women infected with more than one high-risk HPV type were younger, had lower CD4+ lymphocyte counts, and were more likely to be infected with HPV 16 or 18. In adjusted analyses, presence of more than one high-risk HPV type was associated with a two-fold increased risk of abnormal cytology after adjusting for presence of individual high-risk type, age, and CD4+ lymphocyte count (adjusted prevalence ratios 1.88-2.07, all p < 0.001). No single high-risk HPV type was statistically associated with abnormal cytology after adjusting for the presence of more than one high-risk HPV type. Conclusions: In the largest study of cervical HPV genotypes among HIV-infected women in Latin America, infection by high-risk HPV types other than 16 or 18 and infection by more than one high-risk HPV types were common. Infection by more than one high-risk type was more strongly associated with abnormal cervical cytology than any individual high-risk HPV type, highlighting the need for multi-valent HPV vaccines. | |
dc.description.index | MEDLINE | |
dc.description.sponsorship | National Institutes of Health (United States) [T32 AI007474, K24 AI65298, UO1 AI069923, R25 MH087222] | |
dc.description.sponsorship | National Council of Technological and Scientific Development (Brazil) | |
dc.description.sponsorship | Research Agency of the State of Rio de Janeiro (Brazil) | |
dc.description.sponsorship | Brazilian National STD/AIDS Program (Brazil) | |
dc.identifier.citation | BMC CANCER, v.15, article ID 478, 10p, 2015 | |
dc.identifier.doi | 10.1186/s12885-015-1486-4 | |
dc.identifier.issn | 1471-2407 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/12020 | |
dc.language.iso | eng | |
dc.publisher | BIOMED CENTRAL LTD | |
dc.relation.ispartof | BMC Cancer | |
dc.rights | openAccess | |
dc.rights.holder | Copyright BIOMED CENTRAL LTD | |
dc.subject | HPV | |
dc.subject | Women | |
dc.subject | HIV | |
dc.subject | Cervical cancer | |
dc.subject | Epidemiology | |
dc.subject.other | active antiretroviral therapy | |
dc.subject.other | human-immunodeficiency-virus | |
dc.subject.other | squamous intraepithelial lesions | |
dc.subject.other | positive women | |
dc.subject.other | cytological abnormalities | |
dc.subject.other | cell count | |
dc.subject.other | hpv types | |
dc.subject.other | prevalence | |
dc.subject.other | genotypes | |
dc.subject.other | cancer | |
dc.subject.wos | Oncology | |
dc.title | A cross-sectional study of high-risk human papillomavirus clustering and cervical outcomes in HIV-infected women in Rio de Janeiro, Brazil | |
dc.type | article | |
dc.type.category | original article | |
dc.type.version | publishedVersion | |
dspace.entity.type | Publication | |
hcfmusp.affiliation.country | Estados Unidos | |
hcfmusp.affiliation.countryiso | us | |
hcfmusp.author.external | CASTILHO, Jessica L.:Vanderbilt Univ, Div Infect Dis, Sch Med, Nashville, TN 37235 USA | |
hcfmusp.author.external | LUZ, Paula M.:Fundacao Oswaldo Cruz, Inst Nacl Infectol Evandro Chagas, Rio De Janeiro, Brazil | |
hcfmusp.author.external | CAMBOU, Mary Catherine:Univ Calif Los Angeles, David Geffen Sch Med, Div Infect Dis, Los Angeles, CA 90095 USA; Univ Calif Los Angeles, David Geffen Sch Med, Program Global Hlth, Los Angeles, CA 90095 USA | |
hcfmusp.author.external | VANNI, Tazio:Minist Saude, Dept Ciencia & Tecnol, Brasilia, DF, Brazil | |
hcfmusp.author.external | ANDRADE, Angela de:Fundacao Oswaldo Cruz, Inst Nacl Infectol Evandro Chagas, Rio De Janeiro, Brazil | |
hcfmusp.author.external | DERRICO, Monica:Fundacao Oswaldo Cruz, Inst Nacl Infectol Evandro Chagas, Rio De Janeiro, Brazil | |
hcfmusp.author.external | VELOSO, Valdilea G.:Fundacao Oswaldo Cruz, Inst Nacl Infectol Evandro Chagas, Rio De Janeiro, Brazil | |
hcfmusp.author.external | GRINSZTEJN, Beatriz:Fundacao Oswaldo Cruz, Inst Nacl Infectol Evandro Chagas, Rio De Janeiro, Brazil | |
hcfmusp.author.external | FRIEDMAN, Ruth K.:Fundacao Oswaldo Cruz, Inst Nacl Infectol Evandro Chagas, Rio De Janeiro, Brazil | |
hcfmusp.citation.scopus | 17 | |
hcfmusp.contributor.author-fmusphc | JOSE EDUARDO LEVI | |
hcfmusp.description.articlenumber | 478 | |
hcfmusp.description.volume | 15 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 26100400 | |
hcfmusp.origem.scopus | 2-s2.0-84934934252 | |
hcfmusp.origem.wos | WOS:000356580200001 | |
hcfmusp.publisher.city | LONDON | |
hcfmusp.publisher.country | ENGLAND | |
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