Evidence map›Paper›PMID 35089930›Full record

ArticlePLoS neglected tropical diseases2022

Leishmania RNA virus-1 is similarly detected among metastatic and non-metastatic phenotypes in a prospective cohort of American Tegumentary Leishmaniasis.

Braulio Mark Valencia, Rachel Lau, Ruwandi Kariyawasam, Marlene Jara, Ana Pilar Ramos, Mathilde Chantry, Justin T Lana, Andrea K Boggild, Alejandro Llanos-Cuentas

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
–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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Journal of parasitology research · 2026
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  10. Frontiers in cellular and infection microbiology · 2022
    Article
  11. Article
  12. Article
  13. Dissection of the macrophage response towards infection by theFrontiers in cellular and infection microbiology · 2022
    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

9 authors.

Braulio Mark ValenciaKirby Institute, The University of New South Wales (UNSW Sydney), Sydney, Australia.ORCID 0000-0001-6741-3908
Rachel LauPublic Health Ontario Laboratory, Toronto, Canada.
Ruwandi KariyawasamInstitute of Medical Science, University of Toronto, Toronto, Canada.
Marlene JaraInstitute of Tropical Medicine of Antwerp, Antwerp, Belgium.
Ana Pilar RamosInstituto de Medicina Tropical "Alexander von Humboldt", Universidad Peruana Cayetano Heredia, Lima, Peru.
Mathilde ChantryCER Groupe, Aye, Belgium.
Justin T LanaNicholas School of the Environment, Duke University, Durham, North Carolina, United States of America.
Andrea K BoggildInstitute of Medical Science, University of Toronto, Toronto, Canada.
Alejandro Llanos-CuentasInstituto de Medicina Tropical "Alexander von Humboldt", Universidad Peruana Cayetano Heredia, Lima, Peru.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

American Tegumentary Leishmaniasis (ATL) is an endemic and neglected disease of South America. Here, mucosal leishmaniasis (ML) disproportionately affects up to 20% of subjects with current or previous localised cutaneous leishmaniasis (LCL). Preclinical and clinical reports have implicated the Leishmania RNA virus-1 (LRV1) as a possible determinant of progression to ML and other severe manifestations such as extensive cutaneous and mucosal disease and treatment failure and relapse. However, these associations were not consistently found in other observational studies and are exclusively based on cross-sectional designs. In the present study, 56 subjects with confirmed ATL were assessed and followed out for 24-months post-treatment. Lesion biopsy specimens were processed for molecular detection and quantification of Leishmania parasites, species identification, and LRV1 detection. Among individuals presenting LRV1 positive lesions, 40% harboured metastatic phenotypes; comparatively 58.1% of patients with LRV1 negative lesions harboured metastatic phenotypes (p = 0.299). We found treatment failure (p = 0.575) and frequency of severe metastatic phenotypes (p = 0.667) to be similarly independent of the LRV1. Parasite loads did not differ according to the LRV1 status (p = 0.330), nor did Leishmanin skin induration size (p = 0.907) or histopathologic patterns (p = 0.780). This study did not find clinical, parasitological, or immunological evidence supporting the hypothesis that LRV1 is a significant determinant of the pathobiology of ATL.

Indexed as

AdultCohort StudiesHumansLeishmaniaLeishmaniasis, CutaneousLeishmaniasis, MucocutaneousLeishmaniavirusMaleMiddle AgedPhenotypeProspective StudiesTreatment Failure

Identifiers

PMID35089930
PMCPMC8827429

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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.