Evidence map›Paper›PMID 41823984›Full record

ArticleThe Journal of infectious diseases2026

Association Between Female Genital Schistosomiasis and High-Risk Human Papillomavirus Among Women of Reproductive Age in Zambia: The Schista Study.

Olimpia Lamberti, Rhoda Ndubani, Jennifer Fitzpatrick, Emily Webb, Nkatya Kasese, Beatrice Nyondo, Barry Kosloff, Maina Cheeba, Philippe Mayaud, Morgan E Lemin and 14 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. 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

24 authors.

Olimpia LambertiDepartment of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0009-0004-6650-6124
Rhoda NdubaniZambart, Lusaka, Zambia.
Jennifer FitzpatrickZambart, Lusaka, Zambia.
Emily WebbDepartment of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-4019-7456
Nkatya KaseseZambart, Lusaka, Zambia.
Beatrice NyondoZambart, Lusaka, Zambia.
Barry KosloffZambart, Lusaka, Zambia.
Maina CheebaZambart, Lusaka, Zambia.
Philippe MayaudDepartment of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Morgan E LeminDepartment of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0009-0001-2098-2473
Pytsje T HoekstraLeiden University Centre for Infectious Diseases, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0002-7285-9223
Govert Van DamLeiden University Centre for Infectious Diseases, Leiden University Medical Centre, Leiden, The Netherlands.
Paul CorstjensDepartment of Cell and Chemical Biology, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0002-0004-0526
Lisette Van LieshoutLeiden University Centre for Infectious Diseases, Leiden University Medical Centre, Leiden, The Netherlands.
Bonnie WebsterDepartment of Science, Natural History Museum, London, United Kingdom.ORCID 0000-0003-0930-9314
Helen AylesDepartment of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0003-4108-2842
Isaiah HansingoLivingstone University Teaching Hospital, Livingstone, Zambia.
Bodo RandrianasoloAssociation K'OLO VANONA, Antananarivo, Madagascar.
Dingase KuwembaCentre for Health, Agriculture and Development Research and Consulting (CHAD), Blantyre, Malawi.
Bellington VwalikaUniversity of Zambia, Lusaka, Zambia.
Paul KamfwaUniversity Teaching Hospital, Cancer Disease Hospital, Lusaka, Zambia.
Kwame ShanaubeZambart, Lusaka, Zambia.
Helen KellyDepartment of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Amaya L BustinduyDepartment of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Funding

European UnionNagasaki UniversityUK Department for International DevelopmentUK Medical Research Council
6 · The paper itself

Abstract

backgroundFemale genital schistosomiasis (FGS), a gynecological disease caused by Schistosoma haematobium egg deposition in the female genital tract, is prevalent in sub-Saharan Africa, the region with the highest cervical cancer burden globally. Persistent high-risk human papillomavirus (HR-HPV) infection is necessary for cervical cancer development. We determined the association between FGS and HR-HPV genotypes in Zambian women.

methodsSexually active women aged 15-50 years, not menstruating or pregnant, were recruited at home and provided 2 cervicovaginal self-swabs, urine sample, and HIV and Trichomonas vaginalis self-tests, and completed a questionnaire. In clinic, midwives collected cervicovaginal swabs and cervical images with point-of-care colposcopy (EVA System, MobileODT). Swabs were analyzed for 14 HR-HPV types (GeneXpert) and Schistosoma DNA (ITS-2 real-time polymerase chain reaction [qPCR]); urine was analyzed for Schistosoma ova by microscopy and circulating anodic antigen. Visual FGS was defined as colposcopic identification of specific genital lesions, and molecular FGS as Schistosoma-positive cervicovaginal qPCR.

resultsAmong 2532 women (median age, 28 [interquartile range, 22-36] years) recruited at home, 1694 (67%) completed clinic follow-up. Prevalence of visual FGS, molecular FGS, and HR-HPV was 35.2% (595/1691), 6.5% (165/2532), and 28.7% (690/2401), respectively. Molecular FGS was weakly associated with all HR-HPV (adjusted odds ratio [aOR], 1.3 [95% confidence interval {CI}, .9-1.9]). Women with molecular FGS were more likely to test positive for HR-HPV types 16/18/45 (aOR, 1.7 [95% CI, 1.0-2.8]). No association was observed between visual FGS and HR-HPV infection (95% CI, .7-1.1).

conclusionsThis is the first study to jointly screen for FGS and HR-HPV in Zambia, reporting an association between oncogenic HR-HPV types and molecular FGS.

Indexed as

Human Papillomavirus VirusesPapillomaviridaePapillomavirus InfectionsSchistosomiasis haematobiaAdolescentAdultAnimalsFemaleGenotypeHumansMiddle AgedPrevalenceSchistosoma haematobiumYoung AdultZambiafemale genital schistosomiasishigh-risk human papillomavirusneglected tropical diseasessexual and reproductive healthsub-Saharan Africa

Identifiers

PMID41823984
PMCPMC13537139

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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.