Evidence map›Paper›PMID 31772506›Full record

ArticleMediators of inflammation2019

Neutrophil Extracellular Trap Components Associate with Infarct Size, Ventricular Function, and Clinical Outcome in STEMI.

Ragnhild Helseth, Christian Shetelig, Geir Øystein Andersen, Miriam Sjåstad Langseth, Shanmuganathan Limalanathan, Trine B Opstad, Harald Arnesen, Pavel Hoffmann, Jan Eritsland, Ingebjørg Seljeflot

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

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  20. Neutrophil extracellular traps: a catalyst for atherosclerosis.Molecular and cellular biochemistry · 2024
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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

10 authors at 2 institutions in 1 country.

Ragnhild HelsethCenter for Clinical Heart Research, Oslo University Hospital Ullevål, Norway.ORCID https://orcid.org/0000-0001-5012-9214
Christian SheteligDepartment of Cardiology, Oslo University Hospital Ullevål, Norway.
Geir Øystein AndersenDepartment of Cardiology, Oslo University Hospital Ullevål, Norway.
Miriam Sjåstad LangsethCenter for Clinical Heart Research, Oslo University Hospital Ullevål, Norway.
Shanmuganathan LimalanathanThe National Association for Heart and Lung Disease (LHL) Hospital, Gardermoen, Norway.
Trine B OpstadCenter for Clinical Heart Research, Oslo University Hospital Ullevål, Norway.
Harald ArnesenCenter for Clinical Heart Research, Oslo University Hospital Ullevål, Norway.
Pavel HoffmannDepartment of Cardiology, Oslo University Hospital Ullevål, Norway.ORCID https://orcid.org/0000-0003-1287-9174
Jan EritslandDepartment of Cardiology, Oslo University Hospital Ullevål, Norway.
Ingebjørg SeljeflotCenter for Clinical Heart Research, Oslo University Hospital Ullevål, Norway.ORCID https://orcid.org/0000-0003-4071-3358
Oslo University Hospital · NOLandsforeningen for hjerte- og lungesyke · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe relevance of neutrophil extracellular traps (NETs) in acute ST-elevation myocardial infarction (STEMI) is unclear. We explored the temporal profile of circulating NET markers and their associations to myocardial injury and function and to adverse clinical events in STEMI patients. METHODS AND

resultsIn 259 patients, blood samples were drawn before and after PCI, on day 1, and after 4 months. Double-stranded deoxyribonucleic acid (dsDNA) and myeloperoxidase-DNA (MPO-DNA) were measured in serum by a nucleic acid stain and ELISA. Cardiac magnetic resonance imaging assessed microvascular obstruction (MVO), area at risk, infarct size, myocardial salvage index, left ventricular ejection fraction (LVEF), and change in indexed left ventricular end-diastolic volume (LVEDVi). Clinical events were registered after 12 months. dsDNA and MPO-DNA levels were highest before PCI, with reduced levels thereafter (all

conclusionsHigh day 1 dsDNA levels after STEMI were associated with myocardial infarct size, adverse left ventricular remodeling, and clinical outcome. Although the origin of dsDNA could be discussed, these observations indicate a potential role for dsDNA in acute myocardial ischemia. This trial is registered with S-08421d, 2008/10614 (Regional Committee for Medical Research Ethics in South-East Norway (2008)).

Indexed as

AgedDNAExtracellular TrapsFemaleHumansMaleMiddle AgedMyocardial InfarctionST Elevation Myocardial InfarctionDNA

Identifiers

PMID31772506
PMCPMC6854936
OpenAlexW2980823855

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.