Evidence map›Paper›PMID 26758266›Full record

ArticleBMJ open2016

Influence of pre-existing inflammation on the outcome of acute coronary syndrome: a cross-sectional study.

Jacob Odeberg, Michael Freitag, Henrik Forssell, Ivar Vaara, Marie-Louise Persson, Håkan Odeberg, Anders Halling, Lennart Råstam, Ulf Lindblad

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Cardioprotective Effect ofInternational journal of molecular sciences · 2025
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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 5 institutions in 2 countries.

Jacob OdebergDepartment of Proteomics, KTH, Science for Life Laboratory Stockholm, Solna, Sweden Centre for Hematology, Karolinska University Hospital, Stockholm, Sweden.
Michael FreitagDepartment of Clinical Sciences in Malmö, Lund University, Malmö, Sweden.
Henrik ForssellBlekinge Centre of Competence, Karlskrona, Sweden.
Ivar VaaraDepartment of Laboratory Medicine, Blekinge County Hospital, Karlskrona, Sweden.
Marie-Louise PerssonDepartment of Laboratory Medicine, Blekinge County Hospital, Karlskrona, Sweden.
Håkan OdebergBlekinge Centre of Competence, Karlskrona, Sweden.
Anders HallingResearch Unit of General Practice, University of Southern Denmark, Odense, Denmark.
Lennart RåstamDepartment of Clinical Sciences in Malmö, Lund University, Malmö, Sweden.
Ulf LindbladDepartment of Community Medicine/Primary Health Care, University of Gothenburg, Göteborg, Sweden.
Region Blekinge · SELund University · SEKarolinska University Hospital · SEUniversity of Gothenburg · SEUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesInflammation is a well-established risk factor for the development of coronary artery disease (CAD) and acute coronary syndrome (ACS). However, less is known about its influence on the outcome of ACS. The aim of this study was to determine if blood biomarkers of inflammation were associated specifically with acute myocardial infarction (MI) or unstable angina (UA) in patients with ACS.

designCross-sectional study.

settingPatients admitted to the coronary care unit, via the emergency room, at a central county hospital over a 4-year period (1992-1996).

participantsIn a substudy of Carlscrona Heart Attack Prognosis Study (CHAPS) of 5292 patients admitted to the coronary care unit, we identified 908 patients aged 30-74 years, who at discharge had received the diagnosis of either MI (527) or UA (381).

main outcome measuresMI or UA, based on the diagnosis set at discharge from hospital.

resultsWhen adjusted for smoking, age, sex and duration of chest pain, concentrations of plasma biomarkers of inflammation (high-sensitivity C reactive protein>2 mg/L (OR=1.40 (1.00 to 1.96) and fibrinogen (p for trend=0.035)) analysed at admission were found to be associated with MI over UA, in an event of ACS. A strong significant association with MI over UA was found for blood cell markers of inflammation, that is, counts of neutrophils (p for trend<0.001), monocytes (p for trend<0.001) and thrombocytes (p for trend=0.021), while lymphocyte count showed no association. Interestingly, eosinophil count (p for trend=0.003) was found to be significantly lower in patients with MI compared to those with UA.

conclusionsOur results show that, in patients with ACS, the blood cell profile and degree of inflammation at admission was associated with the outcome. Furthermore, our data suggest that a pre-existing low-grade inflammation may dispose towards MI over UA.

Indexed as

Acute Coronary SyndromeAdultAgedAngina, UnstableBiomarkersC-Reactive ProteinCross-Sectional StudiesDisease ProgressionFemaleFibrinogenHumansInflammationLeukocyte CountMaleMiddle AgedMyocardial InfarctionBiomarkersC-Reactive ProteinFibrinogenSerum Amyloid A Proteinacute coronary syndromeInflammation

Identifiers

PMID26758266
PMCPMC4716249
OpenAlexW2262638096

What OpenQuestion holds

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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.