Evidence map›Paper›PMID 38053036›Full record

ArticleBMC infectious diseases2023

Association of PTX3 gene polymorphisms and PTX3 plasma levels with leprosy susceptibility.

Ana Clara Cadidé Gonzaga Moraes, Renata Clesia Feitosa Viana da Luz, André Luís Magalhães Fernandes, Milena Xavier Silva Barbosa, Lorena Viana de Andrade, Anderson da Costa Armstrong, Carlos Dornels Freire de Souza, Rodrigo Feliciano do Carmo

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 24% of its field
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Observational
  4. Review
  5. Review
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

8 authors at 2 institutions in 1 country.

Ana Clara Cadidé Gonzaga MoraesPostgraduate Program in Health and Biological Sciences, Federal University of the São Francisco Valley (UNIVASF), Pernambuco, Brazil.
Renata Clesia Feitosa Viana da LuzPostgraduate Program in Health and Biological Sciences, Federal University of the São Francisco Valley (UNIVASF), Pernambuco, Brazil.
André Luís Magalhães FernandesFoundation of Hematology and Hemotherapy of Bahia (HEMOBA), Bahia, Brazil.
Milena Xavier Silva BarbosaPostgraduate Program in Biosciences, Federal University of the São Francisco Valley (UNIVASF), Pernambuco, Brazil.
Lorena Viana de AndradePostgraduate Program in Biosciences, Federal University of the São Francisco Valley (UNIVASF), Pernambuco, Brazil.
Anderson da Costa ArmstrongCollege of Medicine, Federal University of the São Francisco Valley (UNIVASF), Av. José de Sá Maniçoba, s/n, Centro, Petrolina, PE, Brazil.
Carlos Dornels Freire de SouzaCollege of Medicine, Federal University of the São Francisco Valley (UNIVASF), Av. José de Sá Maniçoba, s/n, Centro, Petrolina, PE, Brazil.
Rodrigo Feliciano do CarmoPostgraduate Program in Health and Biological Sciences, Federal University of the São Francisco Valley (UNIVASF), Pernambuco, Brazil. rodrigo.carmo@univasf.edu.br.
Universidade Federal do Vale do São Francisco · BRFundação Hospitalar de Hematologia e Hemoterapia do Amazonas · BR

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco IBPG-1896-4.03/21 and IBPG-1902-4.03/22
6 · The paper itself

Abstract

backgroundPentraxin 3 (PTX3) is a soluble pattern recognition receptor that plays a crucial role in modulating the inflammatory response and activating the complement system. Additionally, plasma PTX3 has emerged as a potential biomarker for various infectious diseases. The aim of this study was to evaluate the association of PTX3 gene polymorphisms and PTX3 plasma levels with susceptibility to leprosy and clinical characteristics.

methodsPatients with leprosy from a hyperendemic area in the Northeast Region of Brazil were included. Healthy household contacts and healthy blood donors from the same geographical area were recruited as a control group. The rs1840680 and rs2305619 polymorphisms of PTX3 were determined by real-time PCR. Plasma levels of PTX3 were determined by ELISA.

resultsA total of 512 individuals were included. Of these, 273 were patients diagnosed with leprosy; 53 were household contacts, and 186 were healthy blood donors. No association was observed between PTX3 polymorphisms and susceptibility to leprosy or development of leprosy reaction or physical disability. On the other hand, plasma levels of PTX3 were significantly higher in patients with leprosy when compared to household contacts (p = 0.003) or blood donors (p = 0.04). It was also observed that PTX3 levels drop significantly after multidrug therapy (p < 0.0001).

conclusionsOur results suggest that PTX3 may play an important role in the pathogenesis of leprosy and point to the potential use of this molecule as an infection marker.

Indexed as

Leprostatic AgentsLeprosyBiomarkersC-Reactive ProteinDrug Therapy, CombinationHumansPentraxinsPolymorphism, Single NucleotideBiomarkersC-Reactive ProteinLeprostatic AgentsPentraxinsBiomarkersLeprosyPentraxinPolymorphismSNP

Identifiers

PMID38053036
PMCPMC10699025
OpenAlexW4389331405

What OpenQuestion holds

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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.