Evidence map›Paper›PMID 36277769›Full record

ReviewFrontiers in cardiovascular medicine2022

Biomarker-based approach to determine etiology and severity of pulmonary hypertension: Focus on microRNA.

Sylwester Rogula, Bartosz Pomirski, Norbert Czyżak, Ceren Eyileten, Marek Postuła, Łukasz Szarpak, Krzysztof J Filipiak, Marcin Kurzyna, Miłosz Jaguszewski, Tomasz Mazurek and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Sylwester Rogula1st Chair and Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Bartosz Pomirski1st Chair and Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Norbert Czyżak1st Chair and Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Ceren EyiletenDepartment of Experimental and Clinical Pharmacology, Centre for Preclinical Research and Technology, Medical University of Warsaw, Warsaw, Poland.
Marek PostułaDepartment of Experimental and Clinical Pharmacology, Centre for Preclinical Research and Technology, Medical University of Warsaw, Warsaw, Poland.
Łukasz SzarpakDepartment of Outcomes Research, Maria Skłodowska-Curie Medical Academy in Warsaw, Warsaw, Poland.
Krzysztof J FilipiakInstitute of Clinical Sciences, Maria Skłodowska-Curie Medical Academy in Warsaw, Warsaw, Poland.
Marcin KurzynaDepartment of Pulmonary Circulation, Thromboembolic Diseases and Cardiology, Centre of Postgraduate Medical Education, European Health Centre Otwock, Otwock, Poland.
Miłosz Jaguszewski1st Department of Cardiology, Medical University of Gdańsk, Gdańsk, Poland.
Tomasz Mazurek1st Chair and Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Marcin Grabowski1st Chair and Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Aleksandra Gąsecka1st Chair and Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Medical University of Warsaw · PLGdańsk Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is characterized by remodeling of the pulmonary arteries, and defined by elevated pulmonary arterial pressure, measured during right heart catheterization. There are three main challenges to the diagnostic and therapeutic process of patients with PAH. First, it is difficult to differentiate particular PAH etiology. Second, invasive diagnostic is required to precisely determine the severity of PAH, and thus to qualify patients for an appropriate treatment. Third, the results of treatment of PAH are unpredictable and remain unsatisfactory. MicroRNAs (miRNAs) are small non-coding RNAs that regulate post transcriptional gene-expression. Their role as a prognostic, and diagnostic biomarkers in many different diseases have been studied in recent years. MiRNAs are promising novel biomarkers in PAH due to their activity in various molecular pathways and processes underlying PAH. Lack of biomarkers to differentiate between particular PAH etiology and evaluate the severity of PAH, as well as paucity of therapeutic targets in PAH open a new field for the possibility to use miRNAs in these applications. In our article, we discuss the potential of miRNAs use as diagnostic tools, prognostic biomarkers and therapeutic targets in PAH.

Indexed as

biomarkermicroRNAmiRNAPAHpulmonary arterial hypertension

Identifiers

PMID36277769
PMCPMC9582157
OpenAlexW4302299445

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.