<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mbulawa ZZA</submitter><funding>USAID PEPFAR</funding><funding>PEPFAR</funding><pagination>56-60</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5886871</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2</volume><pubmed_abstract>This study investigated the performance of Cepheid Xpert human papillomavirus (HPV) assay in South African human immunodeficiency virus (HIV)-infected women and compared its performance with that of hybrid capture-2 (hc2).&lt;h4>Methods&lt;/h4>Stored cervical specimens from HIV-infected women that had previously been tested using hc2 were tested using Xpert.&lt;h4>Results&lt;/h4>The overall HR-HPV prevalence was found to be 62.0% (720/1161) by Xpert and 61.2% (711/1161) by hc2. 13.6% (158/1161) were HPV16 positive, 18.8% (218/1161) were HPV18/45, 37.3% (434/1161) were HPV31/33/35/52/58, 12.7% (147/1161) were HPV51/59 and 23.3% (270/1161) were HPV39/68/56/66. Overall agreement with hc2 was 90%; Cohen's kappa was 0.78 (95% CI 0.74-0.82) indicating substantial agreement. Detection of HPV16, HPV18/45, and HPV31/33/35/52/58 were independently associated with cervical intraepithelial neoplasia (CIN)-2+ (P&lt;0.0001 for each); while HPV51/59 and HPV39/68/56/66 were not. Women infected with HPV16, HPV18/45 or HPV31/33/35/52/58 were found to have significantly higher amounts of HPV DNA detected for those with CIN2+ compared to those without CIN2+, P&lt;0.0001 for each. Xpert and hc2 were similarly sensitive (88.3% and 91.5%, respectively) and specific (48.4% and 51.0%) for CIN2+ and CIN3 (sensitivity: 95.8% and 97.9%; specificity: 41.4% and 42.8%).&lt;h4>Conclusions&lt;/h4>Xpert is a promising screening test in HIV-infected women that performs similarly to hc2.</pubmed_abstract><journal>Papillomavirus research (Amsterdam, Netherlands)</journal><pubmed_title>Xpert human papillomavirus test is a promising cervical cancer screening test for HIV-seropositive women.</pubmed_title><pmcid>PMC5886871</pmcid><funding_grant_id>674-A-00-08-00007-00</funding_grant_id><pubmed_authors>Mbulawa ZZA</pubmed_authors><pubmed_authors>Faesen M</pubmed_authors><pubmed_authors>Goeieman B</pubmed_authors><pubmed_authors>Levin S</pubmed_authors><pubmed_authors>Chibwesha CJ</pubmed_authors><pubmed_authors>Williamson AL</pubmed_authors><pubmed_authors>Wilkin TJ</pubmed_authors><pubmed_authors>Williams S</pubmed_authors><pubmed_authors>Smith JS</pubmed_authors><pubmed_authors>Swarts A</pubmed_authors><pubmed_authors>Firnhaber C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Xpert human papillomavirus test is a promising cervical cancer screening test for HIV-seropositive women.</name><description>This study investigated the performance of Cepheid Xpert human papillomavirus (HPV) assay in South African human immunodeficiency virus (HIV)-infected women and compared its performance with that of hybrid capture-2 (hc2).&lt;h4>Methods&lt;/h4>Stored cervical specimens from HIV-infected women that had previously been tested using hc2 were tested using Xpert.&lt;h4>Results&lt;/h4>The overall HR-HPV prevalence was found to be 62.0% (720/1161) by Xpert and 61.2% (711/1161) by hc2. 13.6% (158/1161) were HPV16 positive, 18.8% (218/1161) were HPV18/45, 37.3% (434/1161) were HPV31/33/35/52/58, 12.7% (147/1161) were HPV51/59 and 23.3% (270/1161) were HPV39/68/56/66. Overall agreement with hc2 was 90%; Cohen's kappa was 0.78 (95% CI 0.74-0.82) indicating substantial agreement. Detection of HPV16, HPV18/45, and HPV31/33/35/52/58 were independently associated with cervical intraepithelial neoplasia (CIN)-2+ (P&lt;0.0001 for each); while HPV51/59 and HPV39/68/56/66 were not. Women infected with HPV16, HPV18/45 or HPV31/33/35/52/58 were found to have significantly higher amounts of HPV DNA detected for those with CIN2+ compared to those without CIN2+, P&lt;0.0001 for each. Xpert and hc2 were similarly sensitive (88.3% and 91.5%, respectively) and specific (48.4% and 51.0%) for CIN2+ and CIN3 (sensitivity: 95.8% and 97.9%; specificity: 41.4% and 42.8%).&lt;h4>Conclusions&lt;/h4>Xpert is a promising screening test in HIV-infected women that performs similarly to hc2.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Dec</publication><modification>2025-04-19T08:57:17.143Z</modification><creation>2019-03-26T23:29:16Z</creation></dates><accession>S-EPMC5886871</accession><cross_references><pubmed>29074186</pubmed><doi>10.1016/j.pvr.2016.02.004</doi></cross_references></HashMap>