Evidence map›Paper›PMID 31647805›Full record

ArticlePloS one2019

The N125S polymorphism in the cathepsin G gene (rs45567233) is associated with susceptibility to osteomyelitis in a Spanish population.

Laura Pérez-Is, Marcos G Ocaña, A Hugo Montes, José A Carton, Victoria Álvarez, Álvaro Meana, Joshua Fierer, Eulalia Valle-Garay, Víctor Asensi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Laura Pérez-IsBiochemistry and Molecular Biology, University Medical School, Oviedo, Spain.
Marcos G OcañaBiotechnological and Biomedical Assays Unit, University Medical School Oviedo, Spain.
A Hugo MontesBiochemistry and Molecular Biology, University Medical School, Oviedo, Spain.
José A CartonGroup of Translational Research in Infectious Diseases, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.
Victoria ÁlvarezMolecular Genetics Unit-Nephrology Research Institute, Hospital Universitario Central de Asturias, Oviedo, Spain.
Álvaro MeanaCommunity Center for Blood and Tissues of Asturias, CIBERER U714, Oviedo, Spain.
Joshua FiererInfectious Diseases Section, VAMC and University of California, San Diego, California, United States of America.
Eulalia Valle-GarayBiochemistry and Molecular Biology, University Medical School, Oviedo, Spain.
Víctor AsensiGroup of Translational Research in Infectious Diseases, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.ORCID 0000-0003-4211-456X
Hospital Universitario Central de Asturias · ESUniversidad de Oviedo · ESCentre for Biomedical Network Research on Rare Diseases · ESUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteomyelitis is a bone infection, most often caused by Staphylococcus aureus, in which neutrophils play a key role. Cathepsin G (CTSG) is a bactericidal serine protease stored in the neutrophil azurophilic granules. CTSG regulates inflammation, activating matrix metalloproteinases (MMPs), and coagulation. Lactoferrin (LF), a neutrophil glycoprotein, increases CTSG catalytic activity and induces inflammation. The aim of this study was to analyze a potential association between a CTSG gene polymorphism (Asn125Ser or N125S, rs45567233), that modifies CTSG activity, and could affect susceptibility to, or outcome of, bacterial osteomyelitis.

methodsCTSG N125S polymorphism was genotyped in 329 osteomyelitis patients and 415 controls), Blood coagulation parameters, serum CTSG activity, LF, MMP-1, MMP-13, and soluble receptor activator for nuclear factor κ B ligand (sRANKL) levels were assessed in carriers of the different CTSG genotypes.

resultsCTSG N125S (AG) genotype was significantly more frequent among osteomyelitis patients than controls (15.5% vs. 9.4%, p = 0.014). CTSG N125S variant G allele (AG +GG) was also more frequent among osteomyelitis patients (8.1% vs. 4.7%, p = 0.01). Serum CTSG activity and LF levels were significantly higher in osteomyelitis patients carrying the G allele compared to those with the AA genotype, (p<0.04). Serum MMP-1 was lower in the G allele carriers (p = 0.01). There was no association between these genotypes and clinical characteristics of osteomyelitis, or coagulation parameters, MMP-13, and sRANKL serum levels.

conclusionsDifferences in the CTSG gene might enhance osteomyelitis susceptibility by increasing CTSG activity and LF levels.

Indexed as

Amino Acid SubstitutionPolymorphism, Single NucleotideAgedBase SequenceCathepsin GFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedOsteomyelitisSpainCathepsin G

Identifiers

PMID31647805
PMCPMC6812796
OpenAlexW2981606198

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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.