Evidence map›Paper›PMID 33901223›Full record

ArticlePloS one2021

Self-collected and clinician-collected anal swabs show modest agreement for HPV genotyping.

Racheal S Dube Mandishora, Trine B Rounge, Megan Fitzpatrick, Irene Kraus Christiansen, Ole Herman Ambur, Sonja Lagström, Babill Stray-Pedersen, Massimo Tommasino, Joel Palefsky, Zvavahera M Chirenje

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 32 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 8 institutions in 5 countries.

Racheal S Dube MandishoraDepartment of Medical Microbiology, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe.ORCID 0000-0003-1154-6829
Trine B RoungeDepartment of Research, Cancer Registry of Norway, Oslo, Norway.ORCID 0000-0003-2677-2722
Megan FitzpatrickDepartment of Pathology, University of Wisconsin, Madison, Wisconsin, United States of America.
Irene Kraus ChristiansenDepartment of Microbiology and Infection Control, The Norwegian HPV Reference Laboratory, Akershus University Hospital, Lørenskog, Norway.
Ole Herman AmburFaculty of Health Sciences, OsloMet-Oslo Metropolitan University, Oslo, Norway.
Sonja LagströmDepartment of Research, Cancer Registry of Norway, Oslo, Norway.
Babill Stray-PedersenWomen's Clinic, Rikshospitalet, Oslo University Hospital and Institute of Clinical Medicine, Oslo, Norway.
Massimo TommasinoInfections and Cancer Biology Group, International Agency for Research on Cancer, Lyon, France.
Joel PalefskyDepartment of Medicine, UCSF School of Medicine, San Francisco, CA, United States of America.
Zvavahera M ChirenjeDepartment of Obstetrics and Gynaecology, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe.
University of Oslo · NOUniversity of Zimbabwe · ZWAkershus University Hospital · NOCentre international de recherche sur le cancer · FROsloMet – Oslo Metropolitan University · NOOslo University Hospital · NOUniversity of California, San Francisco · USUniversity of Wisconsin–Madison · US

Funding

UZCHS-Promote Excellence in Research and Faculty Enhanced Career Training (PERFECT Program)D43TW010137 · FIC · COLLEGE OF HEALTH SCIS UNIV OF ZIMBABWE · PI CHIPATO, TSUNGAI · 2015 to 2019
$4.1M
FIC NIH HHS D43 TW010137World Health Organization 001
6 · The paper itself

Abstract

BACKGROUND &

aimWomen with HIV/HPV coinfection and cervical lesions are at increased risk of developing HPV related anal cancer. Self-collection of anal swabs may facilitate HPV molecular testing in anal cancer screening, especially in high-risk groups, and yet it is not adequately studied. We evaluated level of agreement between self-collected anal swabs (SCAS) and clinician-collected anal swabs (CCAS) when used for HPV genotyping. We also described the anal HPV genotype distribution and HIV/HPV coinfection.

methodsWe performed a cross sectional study with participants from a visual-inspection-with-acetic-acid and cervicography (VIAC) clinic, in Harare, Zimbabwe. In a clinic setting, the women aged ≥18 years provided anal swabs in duplicate; first CCAS and then SCAS immediately after. HPV detection and genotyping were performed using next generation amplicon sequencing of a 450bp region of the HPV L1 gene. Level of agreement of HPV genotypes between CCAS and SCAS was calculated using the kappa statistic. McNemar tests were used to evaluate agreement in the proportion of genotypes detected by either method.

resultsThree-hundred women provided 600 samples for HPV genotyping. HPV genotypes were detected in 25% of SCAS and in 22% of CCAS. The most common genotypes with CCAS were HPV52, HPV62 and HPV70 and with SCAS were HPV62, HPV44, HPV52, HPV53 and HPV68. Total HPV genotypes detected in CCAS were more than those detected in SCAS, 32 versus 27. The agreement of HPV genotypes between the two methods was 0.55 in kappa value (k). The test of proportions using McNemar gave a Chi-square value of 0.75 (p = 0.39). Multiple HPV infections were detected in 28/75 and 29/67 women for CCAS and SCAS respectively.

conclusionsSCAS and CCAS anal swabs showed moderate agreement, with no statistically significant difference in the proportion of genotypes detected by either methods. Although the differences between the two methods were not statistically significant, CCAS detected more HPV genotypes than SCAS and more HPV infections were detected in SCAS than in CCAS. Our data suggest that self-collected anal swabs can be used as an alternative to clinician-collected anal swabs for HPV genotyping.

Indexed as

GenotypeHIVAdolescentAdultAgedAged, 80 and overAIDS-Related Opportunistic InfectionsAnal CanalAnus NeoplasmsCoinfectionCross-Sectional StudiesDNA, ViralEarly Detection of CancerFemaleHumansMass ScreeningDNA, Viral

Identifiers

PMID33901223
PMCPMC8075200
OpenAlexW3157117521

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.