Evidence map›Paper›PMID 34897278›Full record

ArticleCell death & disease2021

Circulating miR-184 is a potential predictive biomarker of cardiac damage in Anderson-Fabry disease.

Irene Salamon, Elena Biagini, Paolo Kunderfranco, Roberta Roncarati, Manuela Ferracin, Nevio Taglieri, Elena Nardi, Noemi Laprovitera, Luciana Tomasi, Marisa Santostefano and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Biomarkers for gene therapy clinical trials of lysosomal storage disorders.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. Mitochondrial microRNAs Are Dysregulated in Patients with Fabry Disease.The Journal of pharmacology and experimental therapeutics · 2023
    Article
  13. 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

21 authors at 6 institutions in 1 country.

Irene Salamon *Humanitas Research Hospital - IRCCS, 20089, Rozzano, (MI), Italy.ORCID http://orcid.org/0000-0003-2689-4340
Elena Biagini *Cardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Paolo KunderfrancoHumanitas Research Hospital - IRCCS, 20089, Rozzano, (MI), Italy.ORCID http://orcid.org/0000-0003-3636-3391
Roberta RoncaratiInstitute of Genetics and Biomedical Research - Milan Unit, National Research Council of Italy, 20089, Rozzano, (MI), Italy.
Manuela FerracinDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138, Bologna, Italy.ORCID http://orcid.org/0000-0002-1595-6887
Nevio TaglieriCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Elena NardiCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.ORCID http://orcid.org/0000-0003-4245-912X
Noemi LaproviteraDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138, Bologna, Italy.ORCID http://orcid.org/0000-0002-2737-4665
Luciana TomasiDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138, Bologna, Italy.
Marisa SantostefanoNephrology, Dialysis and Renal Transplant Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Raffaello DitarantoCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Giovanni VitaleCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Elena CavarrettaDepartment of Medico-Surgical Sciences and Biotechnologies, University of Rome Sapienza, 04100, Latina, Italy.
Antonio PisaniDepartment of Public Health - Nephrology Unit, University of Naples Federico II, 80131, Naples, Italy.
Eleonora RiccioDepartment of Public Health - Nephrology Unit, University of Naples Federico II, 80131, Naples, Italy.
Valeria AielloDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138, Bologna, Italy.
Irene CapelliDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138, Bologna, Italy.
Gaetano La MannaDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138, Bologna, Italy.
Nazzareno GalièCardiology Unit, St. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.
Letizia SpinelliDepartment of Advanced Biomedical Sciences, University of Naples Federico II, 80131, Naples, Italy. letspine@unina.it.ORCID http://orcid.org/0000-0002-9774-6268
Gianluigi CondorelliHumanitas Research Hospital - IRCCS, 20089, Rozzano, (MI), Italy. gianluigi.condorelli@hunimed.eu.ORCID http://orcid.org/0000-0003-0481-6843
University of Bologna · ITFederico II University Hospital · ITHumanitas University · ITClinica Mediterranea · ITIRCCS Humanitas Research Hospital · ITUniversity of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enzyme replacement therapy (ERT) is a mainstay of treatment for Anderson-Fabry disease (AFD), a pathology with negative effects on the heart and kidneys. However, no reliable biomarkers are available to monitor its efficacy. Therefore, we tested a panel of four microRNAs linked with cardiac and renal damage in order to identify a novel biomarker associated with AFD and modulated by ERT. To this end, 60 patients with a definite diagnosis of AFD and on chronic ERT, and 29 age- and sex-matched healthy individuals, were enrolled by two Italian university hospitals. Only miR-184 met both conditions: its level discriminated untreated AFD patients from healthy individuals (c-statistic = 0.7522), and it was upregulated upon ERT (P < 0.001). On multivariable analysis, miR-184 was independently and inversely associated with a higher risk of cardiac damage (odds ratio = 0.86; 95% confidence interval [CI] = 0.76-0.98; P = 0.026). Adding miR-184 to a comprehensive clinical model improved the prediction of cardiac damage in terms of global model fit, calibration, discrimination, and classification accuracy (continuous net reclassification improvement = 0.917, P < 0.001; integrated discrimination improvement [IDI] = 0.105, P = 0.017; relative IDI = 0.221, 95% CI = 0.002-0.356). Thus, miR-184 is a circulating biomarker of AFD that changes after ERT. Assessment of its level in plasma could be clinically valuable in improving the prediction of cardiac damage in AFD patients.

Indexed as

Fabry DiseaseMicroRNAsBiomarkersCirculating MicroRNAEnzyme Replacement TherapyHeartHumansBiomarkersCirculating MicroRNAMicroRNAsMIRN184 microRNA, human

Identifiers

PMID34897278
PMCPMC8665928
OpenAlexW4200603178

What OpenQuestion holds

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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.