Evidence map›Paper›PMID 31756302›Full record

ArticleCirculation. Genomic and precision medicine2019

Peripheral Blood RNA Levels of

Maarten Vanhaverbeke, Mélanie Vausort, Denise Veltman, Lu Zhang, Ming Wu, Griet Laenen, Hilde Gillijns, Yves Moreau, Jozef Bartunek, Frans Van De Werf and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Circulation. Genomic and precision medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

37 citing papers in PubMed, 67 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

14 authors at 7 institutions in 6 countries.

Maarten VanhaverbekeDepartment of Cardiovascular Sciences (M. Vanhaverbeke, D.V., M.W., H.G., J.B., F.V.D.W., S.J., P.R.S.).
Mélanie VausortCardiovascular Research Unit, Luxembourg Institute of Health, Strassen (M. Vausort, L.Z., Y.D.).
Denise VeltmanDepartment of Cardiovascular Sciences (M. Vanhaverbeke, D.V., M.W., H.G., J.B., F.V.D.W., S.J., P.R.S.).
Lu ZhangCardiovascular Research Unit, Luxembourg Institute of Health, Strassen (M. Vausort, L.Z., Y.D.).
Ming WuDepartment of Cardiovascular Sciences (M. Vanhaverbeke, D.V., M.W., H.G., J.B., F.V.D.W., S.J., P.R.S.).
Griet LaenenDepartment of Electrical Engineering ESAT, STADIUS Center for Dynamical Systems, Signal Processing and Data Analytics, KU Leuven (G.L., Y.M.).
Hilde GillijnsDepartment of Cardiovascular Sciences (M. Vanhaverbeke, D.V., M.W., H.G., J.B., F.V.D.W., S.J., P.R.S.).
Yves MoreauDepartment of Electrical Engineering ESAT, STADIUS Center for Dynamical Systems, Signal Processing and Data Analytics, KU Leuven (G.L., Y.M.).
Jozef BartunekDepartment of Cardiovascular Sciences (M. Vanhaverbeke, D.V., M.W., H.G., J.B., F.V.D.W., S.J., P.R.S.).
Frans Van De WerfDepartment of Cardiovascular Sciences (M. Vanhaverbeke, D.V., M.W., H.G., J.B., F.V.D.W., S.J., P.R.S.).
Yvan DevauxCardiovascular Research Unit, Luxembourg Institute of Health, Strassen (M. Vausort, L.Z., Y.D.).
Stefan JanssensDepartment of Cardiovascular Sciences (M. Vanhaverbeke, D.V., M.W., H.G., J.B., F.V.D.W., S.J., P.R.S.).
Peter R SinnaeveDepartment of Cardiovascular Sciences (M. Vanhaverbeke, D.V., M.W., H.G., J.B., F.V.D.W., S.J., P.R.S.).
EU-CardioRNA COST Action CA17129
Jisc · GBLuxembourg Institute of Health · LUDynamic Systems (United States) · USEducation Training And Research · USOnze Lieve Vrouwziekenhuis Hospital · BEUniversity of Osijek · HRVSL Dutch Metrology Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe identification of patients with acute myocardial infarction (MI) at risk of subsequent left ventricular (LV) dysfunction remains challenging, but it is important to optimize therapies. The aim of this study was to determine the unbiased RNA profile in peripheral blood of patients with acute MI and to identify and validate new prognostic markers of LV dysfunction.

methodsWe prospectively enrolled a discovery cohort with acute MI (n=143) and performed whole-blood RNA profiling at different time points. We then selected transcripts on admission that related to LV dysfunction at follow-up and validated them by quantitative polymerase chain reaction in the discovery cohort, in an external validation cohort (n=449), and in a representative porcine MI model with cardiac magnetic resonance-based measurements of infarct size and postmortem myocardial pathology (n=33).

resultsRNA profiling in the discovery cohort showed upregulation of genes involved in chemotaxis, IL (interleukin)-6, and NF-κB (nuclear factor-κB) signaling in the acute phase of MI. Expression levels of the majority of these transcripts paralleled the rise in cardiac troponin T and decayed at 30 days. RNA levels of

conclusionsPeripheral blood

Indexed as

AdultAgedAged, 80 and overBiomarkersCohort StudiesFemaleHumansLongitudinal StudiesLysophospholipaseMaleMiddle AgedMyocardial InfarctionOxidoreductases Acting on Sulfur Group DonorsProspective StudiesRNAVentricular Dysfunction, LeftBiomarkersLysophospholipaseOxidoreductases Acting on Sulfur Group Donorsphospholipase B-lipaseQSOX1 protein, humanRNAbiomarkersgene expressioninflammationmyocardial infarctionventricular dysfunction, left

Identifiers

PMID31756302
PMCPMC6922070
OpenAlexW2989814060

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.