Evidence map›Paper›PMID 17593313›Full record

Trial reportClinical research in cardiology : official journal of the German Cardiac Society2007

Lipoprotein-associated phospholipase A2 for early risk stratification in patients with suspected acute coronary syndrome: a multi-marker approach: the North Wuerttemberg and Berlin Infarction Study-II (NOBIS-II).

M Möckel, R Müller, J O Vollert, C Müller, O Danne, R Gareis, T Störk, R Dietz, W Koenig

Registry-linked trialAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Clinical research in cardiology : official journal of the German Cardiac Society, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01498731 (The Effect of Integrating the Biomarker Copeptin Into the Process of Managing Patients With Suspected ACS), which is not on this map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 5% 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.

NCT01498731 nacompletednot on this mapstarted 2011, after this paper: background citation

The Effect of Integrating the Biomarker Copeptin Into the Process of Managing Patients With Suspected ACS

TypeinterventionalSponsorCharite University, Berlin, GermanyRan2011 to 2013Enrolled902ConditionsAcute Myocardial InfarctionArmsDischarge home
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Lipoprotein-associated phospholipase-ATurkish journal of emergency medicine · 2017
    Article
  9. Article
  10. Review
  11. [Cardiac biomarkers in the critically ill].Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2012
    Review
  12. Review
  13. Article
  14. Altered nitric oxide/cGMP platelet signaling pathway in platelets from patients with acute coronary syndromes.Clinical research in cardiology : official journal of the German Cardiac Society · 2010
    Article
  15. Lp-PLA2 Inhibition-The Atherosclerosis Panacea?Pharmaceuticals (Basel, Switzerland) · 2010
    Review
  16. Glycoprotein VI as a prognostic biomarker for cardiovascular death in patients with symptomatic coronary artery disease.Clinical research in cardiology : official journal of the German Cardiac Society · 2010
    Article
  17. Article
  18. Coronary surgery for acute coronary syndrome: which determinants of outcome remain?Clinical research in cardiology : official journal of the German Cardiac Society · 2008
    Article
  19. Review
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 4 institutions in 2 countries.

M MöckelDept. of Cardiology, Charité - University Medicine Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany. martin.moeckel@charite.de
R Müller
J O Vollert
C Müller
O Danne
R Gareis
T Störk
R Dietz
W Koenig
Charité - Universitätsmedizin Berlin · DEOlgahospital · DEAustralian Institute of Tropical Health and Medicine · AUUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsNumerous markers have been identified as useful predictors of major adverse cardiac events (MACE) in patients with suspected acute coronary syndrome (ACS). However, only little is known about the relative benefit of the single markers in risk stratification and the best combination for optimising prognostic power. The aim of the present study was to define the role of the emerging cardiovascular risk marker lipoprotein-associated phospholipase A2 (Lp-PLA2) in a multi-marker approach in combination with troponin I (TnI), NT-proBNP, high sensitivity (hs)CRP, and D-dimer in patients with ACS. METHODS AND

resultsA total of 429 consecutive patients (age 60.5+/-14.1 years, 60.6% male) who were admitted to the emergency room with suspected ACS were analysed in the study. Biochemical markers were measured by immunoassay techniques. All patients underwent point-of-care TnI testing and early coronary angiography if appropriate, in accordance with the current guidelines. Classification and regression trees (CART) and logistic regression techniques were employed to determine the relative predictive power of markers for the primary end-point defined as any of the following events within 42 days after admission: death, non-fatal myocardial infarction, unstable AP requiring admission, admission for decompensated heart failure or shock, percutaneous coronary intervention, coronary artery bypass grafting, life threatening arrhythmias or resuscitation. The incidence of the primary end-point was 13.1%, suggesting a mild to moderate risk population. The best overall risk stratification was obtained using NT-proBNP at a cut-off of 5000 pg/mL (incidence of 40% versus 10.3%, relative risk (RR) 3.9 (95% CI 2.4-6.3)). In the remaining lower risk group with an incidence of 10.3%, further separation was performed using TnI (cut-off 0.14 microg/L; RR=3.1 (95% CI 1.7-5.5) 23.2% versus 7.5%) and again NT-proBNP (at a cut-off of 140 ng/L) in patients with negative TnI (RR=3.2 (95% CI 1.3-7.9), 11.7% versus 3.6%). A final significant stratification in patients with moderately elevated NT-proBNP levels was achieved using Lp-PLA2 at a cut-off of 210 microg/L) (17.9% versus 6.9%; RR=2.6 (95% CI 1.1-6.6)). None of the clinical or ECG variables of the TIMI (Thrombolysis In Myocardial Infarction) risk score provided comparable clinically relevant information for risk stratification.

conclusionsIn the setting of stateof- the-art coronary care for patients with suspected ACS in the emergency room, NT-proBNP, troponin I, and Lp-PLA2 are effective independent markers for risk stratification that proved to be superior to the TIMI risk score. Lp-PLA2 turned out to be a more effective risk marker than hsCRP in these patients.

Indexed as

1-Alkyl-2-acetylglycerophosphocholine EsteraseAcute Coronary SyndromeAgedBiomarkersC-Reactive ProteinFemaleHumansMaleMiddle AgedNatriuretic Peptide, BrainPeptide FragmentsPredictive Value of TestsRisk AssessmentRisk FactorsTroponin I1-Alkyl-2-acetylglycerophosphocholine EsteraseBiomarkersC-Reactive ProteinNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Troponin I

Identifiers

PMID17593313
OpenAlexW2087655610

What OpenQuestion holds

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Registered trials

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.