Evidence map›Paper›PMID 40619747›Full record

ArticleJournal of inherited metabolic disease2025

Expression Profiles of Exosomal miRNAs in Gaucher Patients and Their Association With Severity of Bone Involvement.

Irene Serrano-Gonzalo, Laura López de Frutos, Maria Sancho-Albero, Mercedes Roca-Espiau, Ralf Köhler, Pilar Giraldo

Abstract read
In one paragraph

Article in Journal of inherited metabolic disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

6 authors.

Irene Serrano-GonzaloFundación Española Para el Estudio y Tratamiento de la Enfermedad de Gaucher y Otras Lisosomales (FEETEG), Zaragoza, Spain.ORCID https://orcid.org/0000-0002-7507-9249
Laura López de FrutosFundación Española Para el Estudio y Tratamiento de la Enfermedad de Gaucher y Otras Lisosomales (FEETEG), Zaragoza, Spain.ORCID https://orcid.org/0000-0002-1369-6225
Maria Sancho-AlberoInstituto de Investigación Sanitaria de Aragón (IIS Aragón), Zaragoza, Spain.ORCID https://orcid.org/0000-0001-8762-5457
Mercedes Roca-EspiauFundación Española Para el Estudio y Tratamiento de la Enfermedad de Gaucher y Otras Lisosomales (FEETEG), Zaragoza, Spain.
Ralf KöhlerGaucher Disease Research Group (GIIS-012), Instituto de Investigación Sanitaria de Aragón, Zaragoza, Spain.ORCID https://orcid.org/0000-0001-9563-2913
Pilar GiraldoFundación Española Para el Estudio y Tratamiento de la Enfermedad de Gaucher y Otras Lisosomales (FEETEG), Zaragoza, Spain.ORCID https://orcid.org/0000-0002-8791-1901

Funding

Fundación Española para el Estudio y Terapéutica de la Enfermedad de Gaucher y otras lisosomales (FEETEG) FEETEG-2020-01Sanofi SGZ-2019-12810
6 · The paper itself

Abstract

Bone manifestations are one of the most prevalent complications in patients with Gaucher disease (GD). Bone involvement is evaluated by using imaging methods, and there are different scores to assess its severity. However, there are no biomarkers that allow us to predict these manifestations. In recent years, several miRNAs have been associated with bone involvement and postulated as excellent bioavailable biomarkers. This study aims to identify a miRNA expression profile from plasma exosomes and to associate it with the severity of bone involvement in patients with GD. This study included 60 untreated patients with GD with bone involvement, who were classified according to the S-MRI score into three groups: mild disease (MiBD; S-MRI < 5), moderate disease (MoBD; S-MRI: 5-11), or severe disease (SBD; S-MRI > 11). Plasma exosomes were purified, and miRNAs were extracted and identified by next-generation sequencing (NGS) technology. Differentially expressed miRNAs were validated by droplet digital PCR (ddPCR). In the patients' groups classified by S-MRI, the median ages (Q1-Q3) were: MiBD 19.0 (4.00-40.00), MoBD 40.5 (28.25-56.00), and SBD 37.5 (31.25-47.00) years. When comparing groups, we found 12 differentially expressed exosomal miRNAs. After validation, four miRNAs were identified as differentially expressed: hsa-miR-127-3p, hsa-miR-184, hsa-miR-197-3p, and hsa-miR-660-5p. Notably, hsa-miR-127-3p, hsa-miR-660-5p, and hsa-miR-184 were correlated with the presence of infarcts, necrosis, and the degree of infiltration into the spine, pelvis, and femur. These three miRNAs could serve as bioavailable biomarkers to assess bone disease in GD, and further revalidation with a higher number of patients.

Indexed as

Bone DiseasesExosomesGaucher DiseaseMicroRNAsAdolescentAdultBiomarkersChildChild, PreschoolFemaleGene Expression ProfilingHumansMagnetic Resonance ImagingMaleMiddle AgedSeverity of Illness IndexBiomarkersMicroRNAsbiomarkersbone diseaseexosomesGaucher diseasemiRNA

Identifiers

PMID40619747
PMCPMC12230377

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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.