Evidence map›Paper›PMID 34561944›Full record

ReviewJournal of cellular and molecular medicine2021

Aortic valve disease in diabetes: Molecular mechanisms and novel therapies.

Ileana Manduteanu, Dan Simionescu, Agneta Simionescu, Maya Simionescu

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 38 citations in OpenAlex.

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  15. Aortic valve disease in diabetes: Molecular mechanisms and novel therapies.Journal of cellular and molecular medicine · 2021
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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

4 authors at 2 institutions in 2 countries.

Ileana ManduteanuInstitute of Cellular Biology and Pathology "Nicolae Simionescu" of the Romanian Academy, Bucharest, Romania.
Dan SimionescuDepartment of Bioengineering, Clemson University, Clemson, South Carolina, USA.
Agneta SimionescuDepartment of Bioengineering, Clemson University, Clemson, South Carolina, USA.ORCID 0000-0002-9188-2904
Maya SimionescuInstitute of Cellular Biology and Pathology "Nicolae Simionescu" of the Romanian Academy, Bucharest, Romania.
Clemson University · USRomanian Academy · RO

Funding

Transnational Research Imaging Core (TRI)P30GM131959 · NIGMS · CLEMSON UNIVERSITY · PI VYAVAHARE, NAREN R · 2019 to 2023
$5.9M
Cell and matrix interactions in diabetic vascular tissue engineering modelsR01HL133303 · NHLBI · CLEMSON UNIVERSITY · PI SIMIONESCU, AGNETA · 2018 to 2021
$1.4M
NHLBI NIH HHS R01 HL133303NIGMS NIH HHS P30GM131959-01NIH HHS R01HL133303-02
6 · The paper itself

Abstract

Valve disease and particularly calcific aortic valve disease (CAVD) and diabetes (DM) are progressive diseases constituting a global health burden for all aging societies (Progress in Cardiovascular Diseases. 2014;56(6):565: Circulation Research. 2021;128(9):1344). Compared to non-diabetic individuals (The Lancet. 2008;371(9626):1800: The American Journal of Cardiology. 1983;51(3):403: Journal of the American College of Cardiology. 2017;69(12):1523), the diabetic patients have a significantly greater propensity for cardiovascular disorders and faster degeneration of implanted bioprosthetic aortic valves. Previously, using an original experimental model, the diabetic-hyperlipemic hamsters, we have shown that the earliest alterations induced by these conditions occur at the level of the aortic valves and, with time these changes lead to calcifications and CAVD. However, there are no pharmacological treatments available to reverse or retard the progression of aortic valve disease in diabetes, despite the significant advances in the field. Therefore, it is critical to uncover the mechanisms of valve disease progression, find biomarkers for diagnosis and new targets for therapies. This review aims at presenting an update on the basic research in CAVD in the context of diabetes. We provide an insight into the accumulated data including our results on diabetes-induced progressive cell and molecular alterations in the aortic valve, new potential biomarkers to assess the evolution and therapy of the disease, advancement in targeted nanotherapies, tissue engineering and the potential use of circulating endothelial progenitor cells in CAVD.

Indexed as

Diabetes ComplicationsAnimalsAortic ValveAtherosclerosisBiomarkersCombined Modality TherapyDiabetes MellitusDisease ManagementDisease SusceptibilityEndothelial CellsEpithelial-Mesenchymal TransitionExtracellular MatrixHeart Valve DiseasesHumansHyperglycemiaInflammation MediatorsBiomarkersInflammation Mediatorsaortic valvecalcificationdiabetesendothelial progenitor cellshigh glucosenanotherapystem cell therapytissue engineeringvalvular endothelial cellsvalvular interstitial cells

Identifiers

PMID34561944
PMCPMC8505854
OpenAlexW3199674610

What OpenQuestion holds

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LicenceCC BY
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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.