Evidence map›Paper›PMID 39614881›Full record

ArticleImmunogenetics2024

Analysis of Complement Factor H gene polymorphisms and their association with clinical manifestations ofleptospirosis.

Lazara Elena Santiesteban-Lores, Leonardo Moura Midon, ThirsaAlvares Franco, Luciano Marcondes de Oliveira, Sumire Hibi, Yosena Chiani, GdayllonCavalcante Meneses, Elizabeth De Francesco Daher, Denise Moraes Fonseca, Alessandra Pontillo and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Immunogenetics, 2024. 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

11 authors.

Lazara Elena Santiesteban-LoresDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, São Paulo, Brazil.
Leonardo Moura MidonDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, São Paulo, Brazil.
ThirsaAlvares FrancoLaboratory of Zoonoses and Vector-Borne Diseases, Health Surveillance Coordination (COVISA), Municipal Health Secretariat, São Paulo City Hall, São Paulo, Brazil.
Luciano Marcondes de OliveiraLaboratory of Zoonoses and Vector-Borne Diseases, Health Surveillance Coordination (COVISA), Municipal Health Secretariat, São Paulo City Hall, São Paulo, Brazil.
Sumire HibiLaboratory of Zoonoses and Vector-Borne Diseases, Health Surveillance Coordination (COVISA), Municipal Health Secretariat, São Paulo City Hall, São Paulo, Brazil.
Yosena ChianiNational Institute of Respiratory Diseases Dr. E. Coni, ANLIS-UNL, Malbran, Argentina.
GdayllonCavalcante MenesesClinical and Toxicological Analysis Department, School of Pharmacy, Federal University of Ceara, Fortaleza, Ceara, Brazil.
Elizabeth De Francesco DaherClinical and Toxicological Analysis Department, School of Pharmacy, Federal University of Ceara, Fortaleza, Ceara, Brazil.
Denise Moraes FonsecaDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, São Paulo, Brazil.
Alessandra PontilloDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, São Paulo, Brazil.
Lourdes IsaacDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, São Paulo, Brazil. louisaac@icb.usp.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico Proc. # 312654/2021-9Fundação de Amparo à Pesquisa do Estado de São Paulo Proc.# 2017/12924-3
6 · The paper itself

Abstract

Leptospirosis is caused by pathogenic leptospires, posing a significant public health problem. Host susceptibility to Leptospira infection is a multifactorial trait, and the host's genetic background can influence both the establishment of infection and the severity of the disease. Complement Factor H (FH) plays a crucial role in the interaction between pathogenic bacteria and the host. Genetic variants in the FH gene CFH have previously been associated with non-infectious diseases. Here, we aimed to analyze the effect of CFH variants on individual susceptibility to leptospirosis and disease severity. To accomplish this, we sequenced CFH exons 7, 9, 21, 22, and 23 in a case/control cohort (184/162) from two endemic leptospirosis areas in Brazil and Argentina. We identified twenty-one single nucleotide variants (SNVs). In the Brazilian cohort, the intronic variant rs34815383 exhibited a higher frequency in patients than in controls, resulting in a significant association with leptospirosis (p = 0.032; OR: 0.32; 95% CI 0.1-1) and also renal disorder (p = 0.001; OR: 5.3; 95%CI 1.8-15.57). This SNV is reported to be a splicing variant, negatively impacting CFH expression, and has previously been associated with Complement-driven renal disease. A second synonymous variant, rs61822181, was significantly less frequent in patients than in controls (p = 0.002; OR: 7.33; 95% CI 1.59-33.7), representing a protective factor against the development of leptospirosis. Our study represents the first documentation of the frequency of CFH SNVs in South America and identifies the variant rs34815383 T > C as a risk factor for leptospirosis and leptospirosis-related renal complications.

Indexed as

Complement Factor HGenetic Predisposition to DiseaseLeptospirosisPolymorphism, Single NucleotideAdultArgentinaBrazilCase-Control StudiesFemaleHumansLeptospiraMaleMiddle AgedCFH protein, humanComplement Factor HComplement SystemFactor HLeptospirosisPolymorphismRenal injurySNVs

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.