Evidence map›Paper›PMID 28102444›Full record

ArticleHeart and vessels2017

Patients with bicuspid and tricuspid aortic valve exhibit distinct regional microrna signatures in mildly dilated ascending aorta.

Sebastian Albinsson, Alessandro Della Corte, Azra Alajbegovic, Katarzyna K Krawczyk, Ciro Bancone, Umberto Galderisi, Marilena Cipollaro, Marisa De Feo, Amalia Forte

Abstract read
PubMed Publisher
In one paragraph

Article in Heart and vessels, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  14. Enlightening the Association between Bicuspid Aortic Valve and Aortopathy.Journal of cardiovascular development and disease · 2018
    Review
  15. Bio-chemo-mechanics of thoracic aortic aneurysms.Current opinion in biomedical engineering · 2018
    Article
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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 2 institutions in 2 countries.

Sebastian AlbinssonDepartment of Experimental Medical Science, Lund University, Lund, Sweden.
Alessandro Della CorteDepartment of Cardiothoracic Sciences, Second University of Naples, Naples, Italy.
Azra AlajbegovicDepartment of Experimental Medical Science, Lund University, Lund, Sweden.
Katarzyna K KrawczykDepartment of Experimental Medical Science, Lund University, Lund, Sweden.
Ciro BanconeDepartment of Cardiothoracic Sciences, Second University of Naples, Naples, Italy.
Umberto GalderisiDepartment of Experimental Medicine, Section of Biotechnology and Molecular Biology, Second University of Naples, Via L De Crecchio, 7, 80138, Naples, Italy.
Marilena CipollaroDepartment of Experimental Medicine, Section of Biotechnology and Molecular Biology, Second University of Naples, Via L De Crecchio, 7, 80138, Naples, Italy.
Marisa De FeoDepartment of Cardiothoracic Sciences, Second University of Naples, Naples, Italy.
Amalia ForteDepartment of Experimental Medicine, Section of Biotechnology and Molecular Biology, Second University of Naples, Via L De Crecchio, 7, 80138, Naples, Italy. amalia.forte@unina2.it.ORCID http://orcid.org/0000-0002-9652-3249
University of Campania "Luigi Vanvitelli" · ITLund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs are able to modulate gene expression in a range of diseases. We focused on microRNAs as potential contributors to the pathogenesis of ascending aorta (AA) dilatation in patients with stenotic tricuspid (TAV) or bicuspid aortic valve (BAV). Aortic specimens were collected from the 'concavity' and the 'convexity' of mildly dilated AAs and of normal AAs from heart transplant donors. Aortic RNA was analyzed through PCR arrays, profiling the expression of 84 microRNAs involved in cardiovascular disease. An in silico analysis identified the potential microRNA-mRNA interactions and the enriched KEGG pathways potentially affected by microRNA changes in dilated AAs. Distinct signatures of differentially expressed microRNAs are evident in TAV and BAV patients vs. donors, as well as differences between aortic concavity and convexity in patients only. MicroRNA changes suggest a switch of SMC phenotype, with particular reference to TAV concavity. MicroRNA changes potentially affecting mechanotransduction pathways exhibit a higher prevalence in BAV convexity and in TAV concavity, with particular reference to TGF-β1, Hippo, and PI3K/Akt/FoxO pathways. Actin cytoskeleton emerges as potentially affected by microRNA changes in BAV convexity only. MicroRNAs could play distinct roles in BAV and TAV aortopathy, with possible implications in diagnosis and therapy.

Indexed as

Gene Expression ProfilingAdultAgedAortaAortic ValveCase-Control StudiesDilatation, PathologicFemaleGene Expression RegulationHeart Valve DiseasesHumansMaleMechanotransduction, CellularMicroRNAsMiddle AgedTricuspid ValveMicroRNAsAortopathyAscending aortaBicuspid aortic valveMechanotransductionMicroRNAs

Identifiers

PMID28102444
OpenAlexW2575329010

What OpenQuestion holds

Textmetadata
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.