Evidence map›Paper›PMID 35331599›Full record

SynthesisAnais brasileiros de dermatologia

Influence of the presence of mannose-binding lectin polymorphisms on the occurrence of leishmaniasis: a systematic review and meta-analysis.

Wonei de Seixas Vital, Felipe Jules de Araújo Santos, Maurício Leandro Fernandes Gonçalves, Claudia Dantas Comandolli Wyrepkowski, Rajendranath Ramasawmy, Silvania da Conceição Furtado

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Anais brasileiros de dermatologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 96% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 4 institutions in 1 country.

Wonei de Seixas VitalPontifícia Universidade Católica do Paraná, Curitiba, PR, Brazil. Electronic address: wonei.vital@pucpr.edu.br.
Felipe Jules de Araújo SantosFundação de Medicina Tropical Dr. Heitor Vieira Dourado, Manaus, AM, Brazil.
Maurício Leandro Fernandes GonçalvesUniversidade Estácio de Sá, Manaus, AM, Brazil.
Claudia Dantas Comandolli WyrepkowskiInstituto Nacional de Pesquisas da Amazônia, Manaus, AM, Brazil.
Rajendranath RamasawmyFundação de Medicina Tropical Dr. Heitor Vieira Dourado, Manaus, AM, Brazil.
Silvania da Conceição FurtadoDepartment of Morphology, Universidade Federal do Amazonas, Manaus, AM, Brazil.
Fundação de Medicina Tropical · BRUniversidade Federal do Amazonas · BRInstituto Nacional de Pesquisas da Amazônia · BRPontifícia Universidade Católica do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeishmaniasis is caused by an intracellular protozoan of the Leishmania genus. Mannose-binding lectin (MBL) is a serum complement protein and recognizes lipoprotein antigens in protozoa and the bacterial plasma membrane. Nucleotide variants in the promoter region and exon 1 of the MBL gene can influence its expression or change its molecular structure.

objectiveTo evaluate, through a systematic review, case-control studies of the genetic association of variants in the MBL2 gene and the risk of developing leishmaniasis.

methodsThis review carried out a search in PubMed, Science Direct, Cochrane Library, Scopus and Lilacs databases for case-control publications with six polymorphisms in the mannose-binding Lectin gene. The following strategy was used: P = Patients at risk of leishmaniasis; I = Presence of polymorphisms; C = Absence of polymorphisms; O = Occurrence of leishmaniasis. Four case/control studies consisting of 791 patients with leishmaniasis and 967 healthy subjects (Control) are included in this meta-analysis. The association of variants in the mannose-binding Lectin gene and leishmaniasis under the allelic genetic model, -550 (Hvs. L), -221 (X vs. Y), +4 (Q vs. P), CD52 (A vs. D), CD54 (A vs. B), CD57 (A vs. C) and A/O genotype (A vs. O) was evaluated. International Prospective Register of Systematic Reviews (PROSPERO): CRD42020201755.

resultsThe meta-analysis results for any allelic genetic model showed no significant association for the variants within the promoter, the untranslated region, and exon 1, as well as for the wild-type A allele and mutant allele O with leishmaniasis. STUDY LIMITATIONS: Caution should be exercised when interpreting these results, as they are based on a few studies, which show divergent results when analyzed separately.

conclusionsThis meta-analysis showed a non-significant association between the rs11003125, rs7096206, rs7095891, rs5030737, rs1800450, and rs1800451 polymorphisms of the Mannose-binding Lectin gene and leishmaniasis in any allelic and heterogeneous evaluation.

Indexed as

LeishmaniasisMannose-Binding LectinAllelesGenetic Predisposition to DiseaseGenotypeHumansPolymorphism, Single NucleotideMannose-Binding LectinMBL2 protein, humanLeishmaniasisMannose-binding lectinPolymorphism, genetic

Identifiers

PMID35331599
PMCPMC9133304
OpenAlexW4220842232

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.