Evidence map›Paper›PMID 41286869›Full record

ArticleBMC women's health2025

Human papillomavirus (HPV) genotypes extended prevalence in the female population from a city in Northern Chile.

Valeria Escobar, Alejandro Catalán, Verónica Callejas, Roylester Araya, José Rojas, Jonathan García, Armando Alday, Tania Martin, Karol Santoro, Claudia Campillay-Véliz and 1 more

Abstract read
In one paragraph

Article in BMC women's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Valeria EscobarDepartamento de Obstetricia, Facultad de Ciencias de la Salud, Universidad de Antofagasta, Antofagasta, Chile.
Alejandro CatalánDepartamento de Tecnología Médica, Facultad de Ciencias de la Salud, Universidad de Antofagasta, Antofagasta, Chile.
Verónica CallejasDepartamento de Obstetricia, Facultad de Ciencias de la Salud, Universidad de Antofagasta, Antofagasta, Chile.
Roylester ArayaHospital Clínico Universidad de Antofagasta, Antofagasta, Chile.
José RojasDepartamento de Tecnología Médica, Facultad de Ciencias de la Salud, Universidad de Antofagasta, Antofagasta, Chile.
Jonathan GarcíaHospital Clínico Universidad de Antofagasta, Antofagasta, Chile.
Armando AldayHospital Clínico Universidad de Antofagasta, Antofagasta, Chile.
Tania MartinHospital Clínico Universidad de Antofagasta, Antofagasta, Chile.
Karol SantoroDepartamento de Educación, Facultad de Educación, Universidad de Antofagasta, Antofagasta, Chile.
Claudia Campillay-VélizDepartamento de Farmacología, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Christian A MuñozDepartamento de Tecnología Médica, Facultad de Ciencias de la Salud, Universidad de Antofagasta, Antofagasta, Chile. christian.munoz@uantof.cl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCervical cancer is primarily associated with the presence of human papillomavirus (HPV), with high-risk genotypes HPV-16 and HPV-18 being the focus of vaccination programs in developing countries such as Chile. Preventive screening for cervical cancer in women aged 25 to 64 years remains centered on cytological techniques and is primarily performed based on clinical suspicion of cervical lesions. However, extended screening for HPV genotypes using DNA amplification methods is not routinely applied to the Chilean female population yet. This study aimed to determine the prevalence of high- and low-risk HPV genotypes in women without known risk factors in a city in northern Chile.

methodsCervicovaginal brushing samples were obtained from 390 women from Antofagasta city, Northern Chile, aged between 25 and 64 years; genomic DNA was extracted, and multiplex real-time PCR analysis was used to identify a larger group of high- and low-risk HPV genotypes.

resultsAmong 390 samples, HPV prevalence was 36.9%, of which 54.9% were high-risk genotypes, 18.7% were low-risk genotypes, and 26.4% showed mixed infection with both high- and low-risk genotypes. High-risk genotypes 16, 58, 39, and 31 were the most frequently identified among HPV-positive samples. Furthermore, a significant association was observed between HPV presence and both age and suspicion of cervical alteration, and women testing positive for other sexually transmitted infections (STIs) were more likely to acquire HPV.

conclusionsImplementing a screening program that incorporates extended HPV genotyping in Chile, including testing for high-risk genotypes 16, 18, 31, 39, and 58, is crucial to optimize control, early detection, and vaccination efforts for Chilean circulating HPV genotypes that are not covered by the actual vaccine, thus contributing to a more effective reduction in the burden of disease associated with the virus.

Indexed as

PapillomaviridaePapillomavirus InfectionsUterine Cervical NeoplasmsAdultChileDNA, ViralFemaleGenotypeHuman Papillomavirus VirusesHumansMiddle AgedPrevalenceDNA, ViralGenotypingHigh-risk HPVHPV prevalenceHuman papillomavirusLow-risk HPV

Identifiers

PMID41286869
PMCPMC12752438

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.