Evidence map›Paper›PMID 38216639›Full record

ArticleScientific reports2024

Discovery of circulating miRNAs as biomarkers of chronic Chagas heart disease via a small RNA-Seq approach.

Silvina R Villar, Alfonso Herreros-Cabello, Francisco Callejas-Hernández, María C Maza, Javier Del Moral-Salmoral, Mario Gómez-Montes, Héctor O Rodríguez-Angulo, Irene Carrillo, Miguel Górgolas, Pau Bosch-Nicolau and 8 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Vaccines against chronicExpert review of vaccines · 2026
    Review
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 9 institutions in 4 countries.

Silvina R Villar *Instituto de Inmunología Clínica y Experimental de Rosario (IDICER-CONICET-UNR), Rosario, Argentina.
Alfonso Herreros-Cabello *Departamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
Francisco Callejas-Hernández *Departamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
María C MazaDepartamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
Javier Del Moral-SalmoralDepartamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
Mario Gómez-MontesDepartamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
Héctor O Rodríguez-AnguloInstituto Venezolano de Investigaciones Científicas- IVIC, Caracas, 1021, Venezuela.
Irene CarrilloDivision of Infectious Diseases, IIS-Fundación Jiménez Díaz, Madrid, Spain.
Miguel GórgolasDivision of Infectious Diseases, IIS-Fundación Jiménez Díaz, Madrid, Spain.
Pau Bosch-NicolauInternational Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, Vall d'Hebron University Hospital, PROSICS Barcelona, Barcelona, Spain.
Israel MolinaInternational Health Unit Vall d'Hebron-Drassanes, Infectious Diseases Department, Vall d'Hebron University Hospital, PROSICS Barcelona, Barcelona, Spain.
José A Pérez-MolinaNational Referral Unit for Tropical Diseases, Infectious Diseases Department, Ramón y Cajal University Hospital, IRICYS, Madrid, Spain.
Begoña Monge-MailloNational Referral Unit for Tropical Diseases, Infectious Diseases Department, Ramón y Cajal University Hospital, IRICYS, Madrid, Spain.
Oscar A BottassoInstituto de Inmunología Clínica y Experimental de Rosario (IDICER-CONICET-UNR), Rosario, Argentina.
Juan BeloscarCátedra y Servicio de Cardiología, Sección Chagas, Hospital Provincial del Centenario, Rosario, Argentina.
Ana R PérezInstituto de Inmunología Clínica y Experimental de Rosario (IDICER-CONICET-UNR), Rosario, Argentina.
Manuel Fresno *Departamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain.
Núria Gironès *Departamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), 28049, Madrid, Spain. nuria.girones@uam.es.
Centro de Biología Molecular Severo Ochoa · ESCentro de Investigación Biomédica en Red · ESConsejo Nacional de Investigaciones Científicas y Técnicas · ARHospital Universitario Fundación Jiménez Díaz · ESInstituto Cajal · ESHospital Provincial de Rosario · ARInstituto de Biología Molecular y Celular de Rosario · ARInstituto Venezolano de Investigaciones Científicas · VENew York University · US

Funding

Agencia Nacional e Promoción Científica y Tecnológica PICT 2013-1892Consejería de Sanidad, Comunidad de Madrid S-2010/BMD-2332Ministerio de Ciencia, Innovación y Universidades-Agencia Estatal de Investigación and Fondo Europeo de Desarrollo Regional PGC2018-096132-B-I00Ministerio de Economía y competitividad and Fondo Europeo de Desarrollo Regional SAF2015-63868-R (MINECO/FEDER)Ministerio de Economía y competitividad and Fondo Europeo de Desarrollo Regional SAF2016-75988-R (MINECO/FEDER)Red de Investigación de Centros de Enfermedades Tropicales RICET RD12/0018/0004Secretaría de Ciencia y Tecnología, Universidad Nacional de Rosario 1MED410
6 · The paper itself

Abstract

Chagas disease affects approximately 7 million people worldwide in Latin America and is a neglected tropical disease. Twenty to thirty percent of chronically infected patients develop chronic Chagas cardiomyopathy decades after acute infection. Identifying biomarkers of Chagas disease progression is necessary to develop better therapeutic and preventive strategies. Circulating microRNAs are increasingly reliable biomarkers of disease and therapeutic targets. To identify new circulating microRNAs for Chagas disease, we performed exploratory small RNA sequencing from the plasma of patients and performed de novo miRNA prediction, identifying potential new microRNAs. The levels of the new microRNAs temporarily named miR-Contig-1519 and miR-Contig-3244 and microRNAs that are biomarkers for nonchagasic cardiomyopathies, such as miR-148a-3p and miR-224-5p, were validated by quantitative reverse transcription. We found a specific circulating microRNA signature defined by low miR-Contig-3244, miR-Contig-1519, and miR-148a-3 levels but high miR-224-5p levels for patients with chronic Chagas disease. Finally, we predicted in silico that these altered circulating microRNAs could affect the expression of target genes involved in different cellular pathways and biological processes, which we will explore in the future.

Indexed as

Chagas DiseaseCirculating MicroRNAHeart DiseasesMicroRNAsBiomarkersChronic DiseaseHumansRNA-SeqBiomarkersCirculating MicroRNAMicroRNAsMIRN224 microRNA, human

Identifiers

PMID38216639
PMCPMC10786931
OpenAlexW4390823039

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.