<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nitkowski J</submitter><funding>NCATS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>270-275</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10978280</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>51(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Home-based self-sampling may be a viable option for anal cancer screening among sexual minority men (SMM). Yet limited research has compared home-based self-collected with clinician-collected anal swabs for human papillomavirus (HPV) genotyping.&lt;h4>Methods&lt;/h4>The Prevent Anal Cancer Self-Swab Study recruited SMM and transgender persons 25 years and over in Milwaukee, WI to participate in an anal cancer screening study. Participants were randomized to a home or clinic arm. Home-based participants were mailed an anal self-sampling kit to complete and return via postal mail. They were also asked to attend a clinic appointment where a clinician collected an anal swab. Swabs were HPV-genotyped using the SPF 10 -LiPA 25 assay. We analyzed 79 paired self and clinician swabs to determine HPV prevalence, percent agreement, and sensitivity and specificity of the mailed home-based anal self-swab to detect HPV genotypes using the clinician-collected swab as the reference.&lt;h4>Results&lt;/h4>The median number of days between the home and clinic swab was 19 days (range = 2 to 70). Human papillomavirus was detected in 73.3% of self and 75.0% of clinician anal swabs ( P = 0.99). Prevalence of any HPV, any high-risk HPV, any low-risk HPV, and individual HPV types did not significantly differ between self and clinician anal swabs. Agreement between self and clinician swabs was over 90% for 21 of the 25 HPV genotypes. Mailed home-based self-collected swabs had a sensitivity of 94.1% (95% confidence interval, 82.9-99.0) for detection of high-risk HPV versus clinician-collected sampling.&lt;h4>Conclusions&lt;/h4>Mailed home-based self-collected and clinician-collected anal swabs demonstrated high concordance for HPV genotyping.</pubmed_abstract><journal>Sexually transmitted diseases</journal><pubmed_title>Concordance of Human Papillomavirus Genotypes in Mailed Home-Based Self-Collected Versus Clinician-Collected Anal Swabs Among Sexual and Gender Minority Individuals.</pubmed_title><pmcid>PMC10978280</pmcid><funding_grant_id>UL1 TR001436</funding_grant_id><funding_grant_id>R01 CA215403</funding_grant_id><pubmed_authors>Ridolfi T</pubmed_authors><pubmed_authors>Fernandez ME</pubmed_authors><pubmed_authors>Giuliano AR</pubmed_authors><pubmed_authors>Schick V</pubmed_authors><pubmed_authors>Swartz MD</pubmed_authors><pubmed_authors>Nitkowski J</pubmed_authors><pubmed_authors>Chiao E</pubmed_authors><pubmed_authors>Nyitray AG</pubmed_authors><pubmed_authors>Smith JS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Concordance of Human Papillomavirus Genotypes in Mailed Home-Based Self-Collected Versus Clinician-Collected Anal Swabs Among Sexual and Gender Minority Individuals.</name><description>&lt;h4>Background&lt;/h4>Home-based self-sampling may be a viable option for anal cancer screening among sexual minority men (SMM). Yet limited research has compared home-based self-collected with clinician-collected anal swabs for human papillomavirus (HPV) genotyping.&lt;h4>Methods&lt;/h4>The Prevent Anal Cancer Self-Swab Study recruited SMM and transgender persons 25 years and over in Milwaukee, WI to participate in an anal cancer screening study. Participants were randomized to a home or clinic arm. Home-based participants were mailed an anal self-sampling kit to complete and return via postal mail. They were also asked to attend a clinic appointment where a clinician collected an anal swab. Swabs were HPV-genotyped using the SPF 10 -LiPA 25 assay. We analyzed 79 paired self and clinician swabs to determine HPV prevalence, percent agreement, and sensitivity and specificity of the mailed home-based anal self-swab to detect HPV genotypes using the clinician-collected swab as the reference.&lt;h4>Results&lt;/h4>The median number of days between the home and clinic swab was 19 days (range = 2 to 70). Human papillomavirus was detected in 73.3% of self and 75.0% of clinician anal swabs ( P = 0.99). Prevalence of any HPV, any high-risk HPV, any low-risk HPV, and individual HPV types did not significantly differ between self and clinician anal swabs. Agreement between self and clinician swabs was over 90% for 21 of the 25 HPV genotypes. Mailed home-based self-collected swabs had a sensitivity of 94.1% (95% confidence interval, 82.9-99.0) for detection of high-risk HPV versus clinician-collected sampling.&lt;h4>Conclusions&lt;/h4>Mailed home-based self-collected and clinician-collected anal swabs demonstrated high concordance for HPV genotyping.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-07-10T03:08:24.766Z</modification><creation>2025-07-10T03:08:24.766Z</creation></dates><accession>S-EPMC10978280</accession><cross_references><pubmed>38133570</pubmed><doi>10.1097/OLQ.0000000000001916</doi><doi>10.1097/olq.0000000000001916</doi></cross_references></HashMap>