Evidence map›Paper›PMID 42172266›Full record

ArticlePloS one2026

A cross-border seroprevalence study on HBV, HCV, HDV and HIV in remote Amazonian communities on the border between French Guiana and Suriname.

Roxane Schaub, M Sigrid MacDonald-Ottevanger, Stella Hoang, Amandine Pisoni, Karine Bolloré, Barbara Biche, Anfernee Neus, Rikesh Bisnajak, Janke Schinkel, Julie Blanc and 12 more

Abstract read
In one paragraph

Article in PloS one, 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

22 authors.

Roxane SchaubCIC Inserm 1424, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.ORCID https://orcid.org/0000-0001-5742-3280
M Sigrid MacDonald-OttevangerFoundation for Scientific Research Suriname (SWOS), Paramaribo, Suriname.
Stella HoangCIC Inserm 1424, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.
Amandine PisoniPathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, EFS, Antilles University, Montpellier University Hospital, Montpellier, France.
Karine BolloréPathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, EFS, Antilles University, Montpellier University Hospital, Montpellier, France.
Barbara BicheCIC Inserm 1424, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.
Anfernee NeusFaculty of Medicine, Anton de Kom University, Paramaribo, Suriname.
Rikesh BisnajakDepartment of Internal Medicine, Academic Hospital, Paramaribo, Suriname.
Janke SchinkelDepartment of Medical Microbiology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Julie BlancCIC Inserm 1424, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.
Antoon GrunbergFoundation for Scientific Research Suriname (SWOS), Paramaribo, Suriname.
Richard NaldjinanUnité des Maladies Infectieuses et Tropicales, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.
Aude LucarelliCOREVIH Guyane, Institut Santé des Populations en Amazonie, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.
Cyril RousseauCentres Délocalisés de Prévention et de Soins, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.
Céline MichaudCentres Délocalisés de Prévention et de Soins, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.
Melanie GailletCentres Délocalisés de Prévention et de Soins, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.
Soeradj HarkisoenDepartment of Internal Medicine, Academic Hospital, Paramaribo, Suriname.
Emmanuel GordienClinical Microbiology Laboratory, National Reference Centre for Hepatitis B, C and Delta Viruses, Hôpital Avicenne Assistance Publique-Hôpitaux de Paris, Bobigny, France.
Maria PrinsPublic Health Service of Amsterdam, Department of Infectious Diseases, Amsterdam, The Netherlands.
Edouard TuaillonPathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, EFS, Antilles University, Montpellier University Hospital, Montpellier, France.
Mathieu NacherCIC Inserm 1424, Centre Hospitalier Universitaire de Guyane, Cayenne, French Guiana.ORCID https://orcid.org/0000-0001-9397-3204
Stephen VredenFoundation for Scientific Research Suriname (SWOS), Paramaribo, Suriname.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNational epidemiological data are essential to achieve viral hepatitis elimination goals. However, viral hepatitis and HIV epidemiology in French Guiana (FG) and Suriname is mainly limited to urban areas. We therefore assessed the prevalence, associated determinants, and knowledge, attitudes, practices, and beliefs (KAP-B) regarding hepatitis B (HBV), hepatitis C (HCV), hepatitis D (HDV), and HIV in the isolated area of the Maroni River, bordering FG and Suriname.

methodsBetween January 2018 and February 2019, adults (≥18 years) living along the Maroni were enrolled in this cross-sectional study and completed a risk factor and KAP-B questionnaire. Participants were tested for viral hepatitis and HIV using serological and molecular analyses: HBV (HBsAg, anti-HBcore antibodies, anti-HBs, HBV DNA), HCV (HCV-antibodies, HCV RNA), HDV (HDV-antibodies), and HIV (HIV-antibodies/antigen, HIV RNA). Age- and sex-adjusted HBV, HCV, and HIV prevalences were estimated using post-stratification weighting.

findingsAmong 2286 participants, adjusted prevalences were respectively 2.08% (95%CI: 1.49-2.66; n = 46) for HBsAg, 25.6%, (95%CI: 20.89-29.24, n = 646) for resolved HBV infection (negative HBsAg and positive anti-HBcore antibodies), 0.13% (95%CI: 0.0-0.27; n = 5) for HCV-antibodies, and 0.65% (95%CI: 0.0-1.40; n = 12) for HIV-antibodies. There were no HDV infections. HBV exposure (acute or resolved) was independently associated with age (per 10-year increase aOR:1.27, 95%CI: 1.18-1.37, p < 0.0001), males (aOR:1.34, 95%CI: 1.10-1.65, p = 0.006), Maroon (aOR:2.22, 95%CI: 1.27-4.06) or other ethnic groups (aOR:2.94, 95%CI: 1.61-5.59) versus Amerindians, (p = 0.002), and higher education (aOR:0.71, 95%CI: 0.56-0.90, p = 0.005). Older age (per 10-years increase aOR:1.64, 95%CI: 1.11-2.44), p = 0.01) and non-autochthonous origin (aOR:3.81, 95%CI: 1.14-12.26, p = 0.02) were associated with HIV. Less than one in six participants correctly identified viral hepatitis transmission modes.

conclusionHBV, HCV and HIV prevalences along the Maroni River were comparable to urban areas and remain concerning. Knowledge about viral hepatitis was low. Achieving viral hepatitis elimination goals requires awareness campaigns and test-and-treat strategies tailored to hard-to-serve populations.

Indexed as

Hepatitis BHepatitis CHepatitis DHIV InfectionsAdolescentAdultCross-Sectional StudiesFemaleFrench GuianaHepacivirusHepatitis B virusHepatitis Delta VirusHIVHumansMaleMiddle Aged

Identifiers

PMID42172266
PMCPMC13196985

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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.