Evidence map›Paper›PMID 41855184›Full record

SynthesisPLoS neglected tropical diseases2026

Genetic background and immune response in paracoccidioidomycosis: A systematic review and meta-analysis of single nucleotide variants.

Sanderson da Silva Coelho, Wellington Santos Fava, Eva Burger, Ana Carla Pereira-Latini, Alessandra Pontillo, James Venturini

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Sanderson da Silva CoelhoSchool of Medicine, Universidade Federal de Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil.
Wellington Santos FavaSchool of Medicine, Universidade Federal de Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil.
Eva BurgerDepartment of Microbiology and Immunology, Biomedical Sciences Institute, Federal University of Alfenas, Alfenas, Brazil.
Ana Carla Pereira-LatiniLauro de Souza Lima Institute, Bauru, Brazil.
Alessandra PontilloDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
James VenturiniSchool of Medicine, Universidade Federal de Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil.ORCID https://orcid.org/0000-0003-0035-2439

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paracoccidioidomycosis (PCM) is a systemic fungal infection endemic to Latin America, especially Brazil, where it is considered a neglected occupational disease. Caused by Paracoccidioides spp., PCM presents a wide spectrum of clinical manifestations, ranging from localized to severe disseminated forms. This heterogeneity suggests that host-related factors, including genetic background, may influence disease development. Genetic susceptibility to infectious diseases is key to understanding differences in immune responses. In PCM, variants in immune-related genes such as cytokines and pattern recognition receptors may modulate susceptibility and disease progression. This study aimed to review the literature on the association between single nucleotide variants (SNVs) PCM susceptibility, severity, and clinical outcomes. A systematic review followed PRISMA guidelines, searching databases like MEDLINE (PubMed), Cochrane Library, LILACS, SciELO, Web of Science, and Google Scholar. Keywords related to "Paracoccidioidomycosis" and "SNVs" were used. The review included studies on SNVs and PCM susceptibility. The quality of the evidence was assessed with the Cochrane and Joanna Briggs Institute risk of bias tool. We also performed a meta-analysis of studies utilizing identical SNVs. This study is registered on PROSPERO, number CRD42025646417. Two SNVs, Interleukin 10 (IL10) and Vitamin D Receptor (VDR) showed a significant association in individual analyses, but none demonstrated a significant association in the meta-analysis. The main limitations discussed in the studies were insufficient sample size, population heterogeneity, and the composition of control groups. Although some SNVs, particularly in IL10 and VDR, showed significant associations with PCM susceptibility in individual studies, the evidence remains limited. The meta-analyses included only two studies per SNV, resulting in low statistical power and exploratory pooled estimates, largely reflecting small sample sizes, lack of replication, and methodological heterogeneity across studies.

Indexed as

Genetic Predisposition to DiseaseParacoccidioidomycosisPolymorphism, Single NucleotideBrazilHumansParacoccidioidesReceptors, CalcitriolReceptors, Calcitriol

Identifiers

PMID41855184
PMCPMC13001940

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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.