Evidence map›Paper›PMID 40670574›Full record

ArticleScientific reports2025

Association between MBL2 gene polymorphism and protection against leprosy in a population of northeastern brazil: a case-control study.

Karla Regina Celestino Nogueira, Heloisa de Almeida Freitas, Mikael Nikson Vilela Tenório da Paz, Allan Ribeiro Reis Scharf Costa, Isabelle Cavalcante Nunes, Jennifer Lorrane Rijo de Araújo Souza, Emiliano de Oliveira Barreto, Jamylle Nunes de Souza Ferro, Carlos Alberto de Carvalho Fraga, Rodrigo Feliciano do Carmo and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Karla Regina Celestino NogueiraForensic DNA Laboratory, Institute of Biological and Health Sciences (ICBS), Postgraduate Program in Health Sciences (PPGCS), Federal University of Alagoas (UFAL), A/C Simoes Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil.
Heloisa de Almeida FreitasForensic DNA Laboratory, Institute of Biological and Health Sciences (ICBS), Postgraduate Program in Health Sciences (PPGCS), Federal University of Alagoas (UFAL), A/C Simoes Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil.
Mikael Nikson Vilela Tenório da PazMulticenter Postgraduate Program in Biochemistry and Molecular Biology (PPGBqBM), Institute of Chemistry and Biotechnology (IQB), Federal University of Alagoas (UFAL), A. C. Simões Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil.
Allan Ribeiro Reis Scharf CostaForensic DNA Laboratory, Institute of Biological and Health Sciences (ICBS), Postgraduate Program in Health Sciences (PPGCS), Federal University of Alagoas (UFAL), A/C Simoes Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil.
Isabelle Cavalcante NunesForensic DNA Laboratory, Institute of Biological and Health Sciences (ICBS), Postgraduate Program in Health Sciences (PPGCS), Federal University of Alagoas (UFAL), A/C Simoes Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil.
Jennifer Lorrane Rijo de Araújo SouzaForensic DNA Laboratory, Institute of Biological and Health Sciences (ICBS), Postgraduate Program in Health Sciences (PPGCS), Federal University of Alagoas (UFAL), A/C Simoes Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil.
Emiliano de Oliveira BarretoForensic DNA Laboratory, Institute of Biological and Health Sciences (ICBS), Postgraduate Program in Health Sciences (PPGCS), Federal University of Alagoas (UFAL), A/C Simoes Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil.
Jamylle Nunes de Souza FerroForensic DNA Laboratory, Institute of Biological and Health Sciences (ICBS), Postgraduate Program in Health Sciences (PPGCS), Federal University of Alagoas (UFAL), A/C Simoes Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil.
Carlos Alberto de Carvalho FragaMolecular Biology and Genetics Laboratory (LABMEG), Federal University of Alagoas (UFAL), Arapiraca Campus, Av. Manoel Severino Barbosa, S/N, Bom Sucesso, Arapiraca, 57309-005, Alagoas, Brazil.
Rodrigo Feliciano do CarmoCollege of Medicine, Federal University of the São Francisco Valley (UNIVASF), S/N, Centro, Petrolina, 56304-917, Pernambuco, Brazil.
Ana Tércia Paulo SilvaPostgraduate program in Health and Biological Sciences, Federal University of the São Francisco Valley (UNIVASF), Petrolina, 56304-917, Pernambuco, Brazil.
Carolinne de Sales MarquesForensic DNA Laboratory, Institute of Biological and Health Sciences (ICBS), Postgraduate Program in Health Sciences (PPGCS), Federal University of Alagoas (UFAL), A/C Simoes Campus, Lourival Melo Mota Avenue, S/N, Tabuleiro do Martins, Maceió, 57072-970, Alagoas, Brazil. carolinne.marques@icbs.ufal.br.

Funding

CAPES scholarship social demand program 88887.832743/2023-00Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco BPP-0032-2.02/24Research Program for the SUS: shared management in health - PPSUS/Fapeal Nº 06/2020 600300000000195/2021
6 · The paper itself

Abstract

Leprosy is a chronic and neglected infectious disease caused by the bacilli Mycobacterium leprae and Mycobacterium lepromatosis, and is considered a public health problem. The genetic basis of the host is a determining factor in the development of the disease, highlighting genetic mutations in the MBL2 gene. The aim of this study was to investigate the associations of the rs1800450 polymorphism in the MBL2 gene in populations from Northeastern Brazil. A retrospective case-control genetic association study was conducted in the state of Alagoas, with replication in a population from Pernambuco/Bahia. The case group included patients diagnosed with leprosy, whereas the control group included healthy individuals. The participants' DNA was extracted via the salting-out method and genotyped via real-time PCR. The allele and genotypic frequencies of the MBL2 (rs1800450) were obtained and subsequently compared between groups via logistic regression. In the population of Alagoas, 556 individuals were recruited, of which 292 were cases and 264 were healthy controls. A statistically significant association was observed between the SNP rs1800450 at MBL2 gene and protection against leprosy, for both the CT genotype (OR = 0.49, p = 0.001, CI = 0.32-0.75), for the T allele and for T carriers (p = 0.046, OR = 0.51, CI = 0.34-0.78; p = 0.002, OR = 0.51, CI = 0.34-0.78, respectively). However, no association was observed in the replication population. When combining the populations, it continued to show a significant association with protection against leprosy in the CT genotype (p = 0.004, OR = 0.66, CI = 0.51-0.87) and in T carriers (p = 0.009, OR = 0.70, CI = 0.54-0.91) even when adjusted by sex. The SNP rs1800450 in the MBL2 gene was associated with leprosy protection in a population from Northeastern Brazil.

Indexed as

Genetic Predisposition to DiseaseLeprosyMannose-Binding LectinPolymorphism, Single NucleotideAdultAgedAllelesBrazilCase-Control StudiesFemaleGene FrequencyGenetic Association StudiesGenotypeHumansMaleMiddle AgedMannose-Binding LectinMBL2 protein, humanBrazilian populationGeneticsImmunologyMannose-binding lectinSNPs

Identifiers

PMID40670574
PMCPMC12267578

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.