Evidence map›Paper›PMID 41716713›Full record

ArticleFrontiers in oncology2025

Persistently high prevalence of HPV16 and rising prevalence of non-16/18 HR-HPV genotypes in cervical precancer and cancer in Latvia in 2016-2024 shape the severity of cervical disease.

Liba Sokolovska, Karina Biserova, Arta Spridzane, Daira Krisane, Alesja Dudorova, Svetlana Gebrila, Ilvija Krasovska, Dmitry Perminov, Beatrise Orlova, Marta Petrovska and 4 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

14 authors.

Liba SokolovskaInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Karina BiserovaInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Arta SpridzaneInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Daira KrisanePathology Institute, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Alesja DudorovaInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Svetlana GebrilaInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Ilvija KrasovskaOncology Centre of Latvia, Riga East Clinical University Hospital, Riga, Latvia.
Dmitry PerminovE. Gulbis Laboratory Ltd, Riga, Latvia.
Beatrise OrlovaCentrala Laboratorija Ltd, Riga, Latvia.
Marta PetrovskaCentrala Laboratorija Ltd, Riga, Latvia.
Juris JansonsInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Androniks MitildzansInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Jurijs NazarovsPathology Institute, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Maria IsaguliantsInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cervical cancer incidence and mortality in Latvia is one of the highest in Europe, but data on HR-HPV prevalence in cervical disease are lacking. We aimed to investigate HR-HPV prevalence in cervical squamous cell carcinoma (CSCC) and cervical dysplasia (CD), association with disease severity, and prevalence changes over time. Materials & Methods: Cervical tissue samples from 145 patients were retrieved and used for HR-HPV genotyping using two commercially available PCR kits. Results: Only six CD samples were HR-HPV negative (6/66, 9.1%), while all CSCC were positive. Over 50% samples (75/139) harbored one, 33.8% two, 10.1% three, and 2.2% four HR-HPV genotypes. CSCC was more likely to harbor multiple HR-HPVs (p=0.0280). HPV16 remained most prevalent in CSCC and CD and was followed by HPV33 (32/139, 23.0%), HPV39 (13/139, 9.4%), and HPV18 (11/139, 7.9%). CSCC samples were more likely to have high HR-HPV loads (p=0.025). Disease severity expressed as CINI to CSCC grade 3, correlated with HR-HPVs detected (p=0.015, r=0.202) and HPV16 and HPV39 loads (p<0.001, r=0.354; p<0.001, r=0.307). prevalence decreased, insignificantly across the analyzed period, while HPV18 decreased significantly (2016-18: 17.4% vs. 2022-24: 2.2%; p=0.032). HPV66, 45, 39, 31, and 33 (2016-18: 13%; 2022-24:31.1%; p=0.045) increased. Discussion: HPV16 remained the most prevalent HR-HPV, while HPV18 decreased. Other HR-HPV genotypes (HPV 66/45/39/31/33) demonstrated an increase in prevalence. Cervical disease severity was linked to specific HR-HPV loads and the number infecting HR-HPVs. These findings highlight the need for extended HR-HPV genotyping with determination of viral load, and request more epidemiological studies analyzing historical and current samples.

Indexed as

cervical cancercervical dysplasiagenotypingHR-HPVinfection

Identifiers

PMID41716713
PMCPMC12913167

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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.