Evidence map›Paper›PMID 31455368›Full record

ArticleMalaria journal2019

Impact of Duffy polymorphisms on parasite density in Brazilian Amazonian patients infected by Plasmodium vivax.

Rechfy K Abou-Ali, Anamika Dhyani, Alexandre L Terço, Diana M Toro, Katiane S Gomes, Lucianna C Tezza, Monique A Negreiros, Celiane S Batista, Márcia K S Souza, Edalton C B Sanguino and 1 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Relationship between Duffy Genotype/Phenotype and Prevalence ofTropical medicine and infectious disease · 2023
    Review
  5. Article
  6. 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

11 authors at 2 institutions in 1 country.

Rechfy K Abou-AliUniversity of the State of Amazonas, Manaus, Brazil.
Anamika DhyaniUniversity of the State of Amazonas, Manaus, Brazil.
Alexandre L TerçoBlood Center of the Amazon State, HEMOAM, Manaus, Brazil.
Diana M ToroBlood Center of the Amazon State, HEMOAM, Manaus, Brazil.
Katiane S GomesBlood Center of the Amazon State, HEMOAM, Manaus, Brazil.
Lucianna C TezzaBlood Center of the Amazon State, HEMOAM, Manaus, Brazil.
Monique A NegreirosBlood Center of the Amazon State, HEMOAM, Manaus, Brazil.
Celiane S BatistaBlood Center of the Amazon State, HEMOAM, Manaus, Brazil.
Márcia K S SouzaBlood Center of the Amazon State, HEMOAM, Manaus, Brazil.
Edalton C B SanguinoBlood Center of the Amazon State, HEMOAM, Manaus, Brazil.
Sérgio R L AlbuquerqueBlood Center of the Amazon State, HEMOAM, Manaus, Brazil. sergiorlalbuquerque@gmail.com.ORCID http://orcid.org/0000-0002-1581-1135
Fundação Hospitalar de Hematologia e Hemoterapia do Amazonas · BRUniversidade do Estado do Amazonas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Duffy glycoprotein acts as the entry point for merozoites of Plasmodium vivax in the invasion of red blood cells. The host-parasite relationship has revealed new perspectives regarding the association between Duffy polymorphisms that can impact both the parasite density of this Plasmodium and the symptoms of this type of malaria. This study investigates the impact of Duffy polymorphisms on parasite density in patients infected with P. vivax in the Brazilian Amazon region.

methodsGenotypes and Duffy polymorphism allele frequencies were compared in 287 patients with malaria, presenting low, medium and high density of P. vivax. The diagnosis of malaria was performed using a specialized team with a standardized clinical-laboratory method, while the Duffy genotyping was performed through the Bead Chip BioArray system. Both teams are reference services in Brazil.

resultsThe FY*01 and FY*02 alleles were found in all three parasite density classes: low, medium and high, but when these alleles form genotypes with FY*02N.01 and FY*02W.01 alleles, they are found only in patients with low parasite density and low symptomatology. Another interesting finding found in this study is the presence of the genotype FY*02N.01/FY*02W.01 in one of the patients, presenting a very low parasite density and malaria considered subclinical, a genotype which had not been previously described in the literature.

conclusionThe presence of FY*02N.01 and FY*02W.01 alleles may have an impact on the reduction of clinical manifestations in malaria, leading to the development of subclinical malaria, making the infected individual an undetected natural reservoir, which may hinder the eradication of malaria in the Amazon.

Indexed as

Polymorphism, GeneticAdolescentAdultAgedBrazilChildChild, PreschoolDuffy Blood-Group SystemFemaleHumansInfantInfant, NewbornMaleMiddle AgedPlasmodium vivaxPopulation DensityDuffy Blood-Group SystemAlleles DuffyParasite densityPlasmodium vivax

Identifiers

PMID31455368
PMCPMC6712886
OpenAlexW2970422953

What OpenQuestion holds

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LicenceCC BY
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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.