Evidence map›Paper›PMID 29764400›Full record

ArticleBMC cancer2018

Low-cost HPV testing and the prevalence of cervical infection in asymptomatic populations in Guatemala.

Hong Lou, Eduardo Gharzouzi, Sarita Polo Guerra, Joël Fokom Domgue, Julie Sawitzke, Guillermo Villagran, Lisa Garland, Joseph F Boland, Sarah Wagner, Héctor Rosas and 14 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 5 institutions in 3 countries.

Hong LouLaboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, Leidos Biomedical Research, Inc., National Laboratory for Cancer Research, Gaithersburg, MD, USA.
Eduardo GharzouziInstituto de Cancerologia, 6ª Avenida 6-58, Zona11, Guatemala City, Guatemala.
Sarita Polo GuerraInstituto de Cancerologia, 6ª Avenida 6-58, Zona11, Guatemala City, Guatemala.
Joël Fokom DomgueCancer Genetics Branch, Gaithersburg, MD, USA.
Julie SawitzkeLaboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, Leidos Biomedical Research, Inc., National Laboratory for Cancer Research, Gaithersburg, MD, USA.
Guillermo VillagranInstituto de Cancerologia, 6ª Avenida 6-58, Zona11, Guatemala City, Guatemala.
Lisa GarlandLaboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, Leidos Biomedical Research, Inc., National Laboratory for Cancer Research, Gaithersburg, MD, USA.
Joseph F BolandLaboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, Leidos Biomedical Research, Inc., National Laboratory for Cancer Research, Gaithersburg, MD, USA.
Sarah WagnerLaboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, Leidos Biomedical Research, Inc., National Laboratory for Cancer Research, Gaithersburg, MD, USA.
Héctor RosasDepartment of Gynecology and Obstetrics, Hospital General San Juan de Dios, Guatemala City, Guatemala.
Jami TroxlerCancer Research Technology Program, Leidos Biomedical Research, Inc., National Cancer Institute, 8560 Progress Drive, Frederick, MD, 21701, USA.
Heidi McMillenCancer Research Technology Program, Leidos Biomedical Research, Inc., National Cancer Institute, 8560 Progress Drive, Frederick, MD, 21701, USA.
Bailey KessingCancer Research Technology Program, Leidos Biomedical Research, Inc., National Cancer Institute, 8560 Progress Drive, Frederick, MD, 21701, USA.
Enrique AlvirezHospital Central Universitario "Dr. Antonio M Pineda", Lara State, Barquisimeto, Venezuela.
Miriam CastilloInstituto de Cancerologia, 6ª Avenida 6-58, Zona11, Guatemala City, Guatemala.
Hesler MoralesInstituto de Cancerologia, 6ª Avenida 6-58, Zona11, Guatemala City, Guatemala.
Victor ArguetaDepartment of Pathology, Hospital General San Juan de Dios, Guatemala City, Guatemala.
Andert RosinghMedical Laboratory Services, Willemstad, Curaçao.
Femke J H B van Aerde-van NunenMedical Laboratory Services, Willemstad, Curaçao.
Griselda LopezDepartment of Pathology, Hospital General San Juan de Dios, Guatemala City, Guatemala.
Herbert M PinedoFundashon Prevenshon, Willemstad, Curaçao.
Mark SchiffmanCancer Genetics Branch, Gaithersburg, MD, USA.
Michael DeanLaboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Gaithersburg, MD, USA. deanm@mail.nih.gov.ORCID 0000-0003-2234-0631
Roberto OrozcoDepartment of Pathology, Hospital General San Juan de Dios, Guatemala City, Guatemala.
Leidos (United States) · USHospital General San Juan de Dios · GTUniversity of Curaçao · CWCancer Genetics (United States) · USNational Cancer Institute · US

Funding

Laboratory of Translational GenomicsZIACP010201 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI PROKUNINA-OLSSON, LIUDMILA · 2010 to 2025
$91.2M
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

backgroundA low cost and accurate method for detecting high-risk (HR) human papillomavirus (HPV) is important to permit HPV testing for cervical cancer prevention. We used a commercially available HPV method (H13, Hybribio) which was documented to function accurately in a reduced volume of cervical specimen to determine the most prevalent HPV types and the distribution of HPV infections in over 1795 cancer-free women in Guatemala undergoing primary screening for cervical cancer by cytology.

methodsHR-HPV detection was attempted in cervical samples from 1795 cancer-free women receiving Pap smears using the Hybribio™ real-time PCR assay of 13 HR types. The test includes a globin gene internal control. HPV positive samples were sequenced to determine viral type. Age-specific prevalence of HPV was also assessed in the study population.

resultsA total of 13% (226/1717) of women tested HPV+, with 78 samples (4.3%) failing to amplify the internal control. The highest prevalence was found in younger women (< 30 years, 22%) and older ones (≥60 years, 15%). The six most common HR-HPV types among the 148 HPV+ typed were HPV16 (22%), HPV18 (11%), HPV39 (11%), HPV58 (10%), HPV52 (8%), and HPV45 (8%).

conclusionsIn this sample of cancer free women in Guatemala, HPV16 was the most prevalent HR type in Guatemala and the age-specific prevalence curve peaked in younger ages. Women in the 30-59-year age groups had a prevalence of HR-HPV of 8%, however, larger studies to better describe the epidemiology of HPV in Guatemala are needed.

Indexed as

AdolescentAdultAgedAge FactorsAsymptomatic InfectionsCervix UteriEarly Detection of CancerFemaleGenotypeGuatemalaHumansMass ScreeningMiddle AgedPapillomaviridaePapillomavirus InfectionsPrevalenceCervical cancerGuatemalaHPVPrevalenceReal-time PCRScreening

Identifiers

PMID29764400
PMCPMC5952444
OpenAlexW2950855917

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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.