Evidence map›Paper›PMID 34726256›Full record

ArticleMolecular medicine reports2021

Medial tunica degeneration of the ascending aortic wall is associated with specific microRNA changes in bicuspid aortic valve disease.

Calogera Pisano, Antonella Marino Gammazza, Francesca Rappa, Rosario Barone, Rosalinda Allegro, Alessandro Pitruzzella, Alessandra Tagliavia, Virginia Agostara, Giovanni Ruvolo, Francesco Cappello and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
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 at 2 institutions in 1 country.

Calogera Pisano *Cardiac Surgery Unit, Tor Vergata University Hospital, I‑00133 Rome, Italy.
Antonella Marino Gammazza *Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, I‑90100 Palermo, Italy.
Francesca Rappa *Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, I‑90100 Palermo, Italy.
Rosario BaroneDepartment of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, I‑90100 Palermo, Italy.
Rosalinda AllegroDepartment of Statistics, University of Palermo, I‑90100 Palermo, Italy.
Alessandro PitruzzellaDepartment of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, I‑90100 Palermo, Italy.
Alessandra TagliaviaDepartment of Cardiac Surgery, University of Palermo, I‑90100 Palermo, Italy.
Virginia AgostaraDepartment of Cardiac Surgery, University of Palermo, I‑90100 Palermo, Italy.
Giovanni RuvoloCardiac Surgery Unit, Tor Vergata University Hospital, I‑00133 Rome, Italy.
Francesco CappelloCardiac Surgery Unit, Tor Vergata University Hospital, I‑00133 Rome, Italy.
Vincenzo ArganoDepartment of Cardiac Surgery, University of Palermo, I‑90100 Palermo, Italy.
University of Palermo · ITUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ascending aortic diameter is not an accurate parameter for surgical indication in patients with bicuspid aortic valve (BAV). Thus, the present study aimed to identify specific microRNAs (miRNAs/miRs) and their expression levels in aortic wall aneurysm associated with BAV according to severity of medial degeneration and to elucidate the association between the tissue expression levels of the miRNAs with their expression in plasma. Aortic wall and blood specimens were obtained from 38 patients: 12 controls and 26 patients with BAV with ascending aortic aneurysm. Of the patients with BAV, 19 had cusp fusions of right and left, 5 of right and non‑coronary, and 2 of left and non‑coronary. Two groups of patients were identified according to the grade of medial degeneration (MD): Low‑grade D group (LGMD) and high‑grade MD group (HGMD). Expression level of miR‑122, miR‑130, miR‑718 and miR‑486 were validated by reverse transcription‑quantitative PCR in plasma and tissue samples. MD grade was found to be independent from the BAV phenotype. The HGD group showed increased expression levels of MMP‑9 and MMP‑2, and an increase in the number of apoptotic cells. Tissue expression levels of miR‑718 and miR‑122 were lower in the LGMD and HGD groups compared with expression in the control group; the HGD group showed increased levels of miR‑486. Plasma expression levels of miR‑122 were decreased in the LGMD and HGD groups, and miR‑718 was only reduced in the HGD group. On the contrary, expression of miR‑486 was increased in the LGMD and HGD groups. The data suggested that miR‑486 may be considered as a non‑invasive biomarker of aortic wall degeneration. Dysregulation of this putative biomarker may be associated with high risk of dissection and rupture in patients with BAV.

Indexed as

AdultAgedAortaAortic AneurysmAortic ValveBicuspid Aortic Valve DiseaseBiomarkersFemaleGene ExpressionHumansItalyMaleMicroRNAsMiddle AgedTranscriptomeBiomarkersMicroRNAsMIRN122 microRNA, humanMIRN130 microRNA, humanMIRN486 microRNA, humanMIRN718 microRNA, humanascending aortabicuspid aortic valve diseasebiomarkersmicroRNAs

Identifiers

PMID34726256
PMCPMC8569523
OpenAlexW3210479011

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.