Evidence map›Paper›PMID 42853870›Full record

ArticlePLoS neglected tropical diseases2026

Epidemiology of helminth infections in adults in rural rainforest communities of the Nkam-Wouri River Basin, Littoral Region of Cameroon: Implications for NTDs elimination using preventive chemotherapies.

Anita Bate Obi Ebob, Narcisse Victor Tchamatchoua Gandjui, Benjamin Lenz, Emmanuel Ouam, Juluis Visnel Foyet, Amuam Andrew Beng, Fanny Fri Fombad, Franck Noel Nietcho, Manuel Ritter, Indulekha Karunakaran and 10 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2026. 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

20 authors.

Anita Bate Obi EbobParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Narcisse Victor Tchamatchoua GandjuiParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Benjamin LenzUniversity of Bonn, University Hospital Bonn, Institute for Medical Microbiology, Immunology and Parasitology, Bonn, Germany.
Emmanuel OuamParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Juluis Visnel FoyetParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Amuam Andrew BengParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Fanny Fri FombadParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Franck Noel NietchoParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Manuel RitterUniversity of Bonn, University Hospital Bonn, Institute for Medical Microbiology, Immunology and Parasitology, Bonn, Germany.
Indulekha KarunakaranUniversity of Bonn, University Hospital Bonn, Institute for Medical Microbiology, Immunology and Parasitology, Bonn, Germany.
Ndialle Nordine MpongeParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Lucy Cho NchangParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Cheng WangUniversity of Bonn, University Hospital Bonn, Institute for Medical Microbiology, Immunology and Parasitology, Bonn, Germany.
Fonyuy Brandon TahntengParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Jerome Fru ChoParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Mathias Eyong EsumParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Tatiana Djikeussi KatchoParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Achim HoeraufUniversity of Bonn, University Hospital Bonn, Institute for Medical Microbiology, Immunology and Parasitology, Bonn, Germany.
Marc P HübnerUniversity of Bonn, University Hospital Bonn, Institute for Medical Microbiology, Immunology and Parasitology, Bonn, Germany.ORCID https://orcid.org/0000-0001-8885-418X
Samuel WanjiParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic helminth infections cause serious health problems; however, limited data on prevalence and distribution hinder effective control interventions. This study assessed the prevalence, distribution, and risk factors of helminth infections in adults across four health districts (HD) in the Littoral Region of Cameroon, while hypothesizing that helminth infection prevalences are significantly higher in densely forested and wetland forest plantation districts compared to degraded and mosaic plantation forest districts despite over more than two decades of preventive chemotherapy. METHODOLOGY/PRINCIPAL

findingsAdults aged 18 - 65 years residing in the community for ≥ 5 years were recruited across four HDs. Skin snips, thick blood films, and stool samples were examined using the Kato Katz method (stool) and microscopy. Demographic data were analyzed in R. Participants were mainly farmers (79.9%), male (52.9%) and aged 18-49 years (50.7%). Yabassi HD, a densely forested area, recorded the highest prevalence of Loa loa and Mansonella perstans, while Loum HD, a wetland forest plantation area, showed higher prevalence for other helminth groups. Overall infection prevalence was 41.9%, dominated by filariasis (33.3%), with Onchocerca volvulus (23.9%) being most common, followed by M. perstans (11.9%) and L. loa (8.9%). Intestinal nematode prevalence was 9.9%, led by Capillaria spp. (4.6%), Ascaris lumbricoides (2.9%) and Trichuris trichiura (2.7%). Trematode infections included Dicrocoelium dendriticum (6.9%) and Paragonimus spp. (3.5%), while Taenia spp. (3.1%) was the most common cestode. Infections were more frequent in males and individuals over 40 years. Strong associations were observed among parasites with similar life cycles, Filariasis risk increased with age ≥ 50 years and longer residence, whereas recent deworming and higher education reduced the odds. CONCLUSIONS/SIGNIFICANCE: Adult helminth infections pose a public health risk and may serve as transmission reservoirs in child-centred programs. Monitoring and including adults in preventive chemotherapy programs, promoting regular deworming and awareness and using a multi-parasite, multi-pathway strategy will strengthen control and elimination efforts in persistently endemic areas.

Indexed as

HelminthiasisAdolescentAdultAgedAnimalsAnthelminticsCameroonFecesFemaleHelminthsHumansMaleMiddle AgedPrevalenceRainforestRisk FactorsAnthelmintics

Identifiers

PMID42853870
PMCPMC13686460

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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.