Evidence map›Paper›PMID 39159265›Full record

Observational studyPLoS neglected tropical diseases2024

Prevalence of dermal trypanosomes in suspected and confirmed cases of gambiense human African trypanosomiasis in Guinea.

Alseny M'mah Soumah, Mariame Camara, Justin Windingoudi Kaboré, Ibrahim Sadissou, Hamidou Ilboudo, Christelle Travaillé, Oumou Camara, Magali Tichit, Jacques Kaboré, Salimatou Boiro and 10 more

Abstract readObservational Study
In one paragraph

Observational study in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Observational
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.

Alseny M'mah SoumahProgramme National de Lutte contre les Maladies Tropicales Négligées, Ministère de la Santé, Conakry, Guinea.
Mariame CamaraProgramme National de Lutte contre les Maladies Tropicales Négligées, Ministère de la Santé, Conakry, Guinea.
Justin Windingoudi KaboréProgramme National de Lutte contre les Maladies Tropicales Négligées, Ministère de la Santé, Conakry, Guinea.
Ibrahim SadissouINTERTRYP, Université de Montpellier, CIRAD, IRD, Montpellier, France.
Hamidou IlboudoINTERTRYP, Université de Montpellier, CIRAD, IRD, Montpellier, France.
Christelle TravailléTrypanosome Transmission Group, Trypanosome Cell Biology Unit, INSERM U1201, Department of Parasites and Insect Vectors, Institut Pasteur, Université Paris Cité, Paris, France.
Oumou CamaraProgramme National de Lutte contre les Maladies Tropicales Négligées, Ministère de la Santé, Conakry, Guinea.
Magali TichitHistopathology Core Facility, Institut Pasteur, Université Paris Cité, Paris, France.
Jacques KaboréUnité de recherches sur les bases biologiques de la lutte intégrée, Centre International de Recherche-Développement sur l'Elevage en zone Subhumide, Bobo-Dioulasso, Burkina Faso.
Salimatou BoiroParasitology Unit, Institut Pasteur of Guinea, Conakry, Guinea.
Aline CrouzolsTrypanosome Transmission Group, Trypanosome Cell Biology Unit, INSERM U1201, Department of Parasites and Insect Vectors, Institut Pasteur, Université Paris Cité, Paris, France.
Jean Marc Tsagmo NgouneTrypanosome Transmission Group, Trypanosome Cell Biology Unit, INSERM U1201, Department of Parasites and Insect Vectors, Institut Pasteur, Université Paris Cité, Paris, France.
David HardyHistopathology Core Facility, Institut Pasteur, Université Paris Cité, Paris, France.
Aïssata CamaraParasitology Unit, Institut Pasteur of Guinea, Conakry, Guinea.
Vincent JamonneauINTERTRYP, Université de Montpellier, CIRAD, IRD, Montpellier, France.
Annette MacLeodWellcome Centre for Integrative Parasitology, College of Medical, Veterinary, and Life Sciences, Henry Wellcome Building for Comparative Medical Sciences, Glasgow, Scotland, United Kingdom.
Jean-Mathieu BartProgramme National de Lutte contre les Maladies Tropicales Négligées, Ministère de la Santé, Conakry, Guinea.
Mamadou CamaraProgramme National de Lutte contre les Maladies Tropicales Négligées, Ministère de la Santé, Conakry, Guinea.
Bruno BuchetonProgramme National de Lutte contre les Maladies Tropicales Négligées, Ministère de la Santé, Conakry, Guinea.
Brice RotureauTrypanosome Transmission Group, Trypanosome Cell Biology Unit, INSERM U1201, Department of Parasites and Insect Vectors, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0003-0671-8999

Funding

French Government Investissement d’Avenir programme - Laboratoire d’Excellence “Integrative Biology of Emerging Infectious Diseases” ANR-10-LABX-62-IBEIDFrench National Agency for Scientific Research ANR-18-CE15-0012
6 · The paper itself

Abstract

The skin is an anatomical reservoir for African trypanosomes, yet the prevalence of extravascular parasite carriage in the population at risk of gambiense Human African Trypanosomiasis (gHAT) remains unclear. Here, we conducted a prospective observational cohort study in the HAT foci of Forecariah and Boffa, Republic of Guinea. Of the 18,916 subjects serologically screened for gHAT, 96 were enrolled into our study. At enrolment and follow-up visits, participants underwent a dermatological examination and had blood samples and superficial skin snip biopsies taken for examination by molecular and immuno-histological methods. In seropositive individuals, dermatological symptoms were significantly more frequent as compared to seronegative controls. Trypanosoma brucei DNA was detected in the blood of 67% of confirmed cases (22/33) and 9% of unconfirmed seropositive individuals (3/32). However, parasites were detected in the extravascular dermis of up to 71% of confirmed cases (25/35) and 41% of unconfirmed seropositive individuals (13/32) by PCR and/or immuno-histochemistry. Six to twelve months after treatment, trypanosome detection in the skin dropped to 17% of confirmed cases (5/30), whereas up to 25% of unconfirmed, hence untreated, seropositive individuals (4/16) were still found positive. Dermal trypanosomes were observed in subjects from both transmission foci, however, the occurrence of pruritus and the PCR positivity rates were significantly higher in unconfirmed seropositive individuals in Forecariah. The lower sensitivity of superficial skin snip biopsies appeared critical for detecting trypanosomes in the basal dermis. These results are discussed in the context of the planned elimination of gHAT.

Indexed as

SkinTrypanosoma brucei gambienseTrypanosomiasis, AfricanAdolescentAdultChildDNA, ProtozoanFemaleGuineaHumansMaleMiddle AgedPrevalenceProspective StudiesYoung AdultDNA, Protozoan

Identifiers

PMID39159265
PMCPMC11361743

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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.