Evidence map›Paper›PMID 30062164›Full record

ReviewJACC. Basic to translational science2017

Failure to Launch: Targeting Inflammation in Acute Coronary Syndromes.

Jennifer A Rymer, L Kristin Newby

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in JACC. Basic to translational science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04218786 (Outcomes of Low-dose Colchicine in Patients With Myocardial Infarction), which is not on this map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
6.9field-weighted citation impact, top 2% 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.

NCT04218786 phase2withdrawnnot on this mapstarted 2025, after this paper: background citation

Outcomes of Low-dose Colchicine in Patients With Myocardial Infarction: A Randomized Controlled Trial

TypeinterventionalSponsorShifa Tameer-e-Millat UniversityRan2025 to 2026Enrolled0ConditionsMyocardium, Injury, Myocardial Infarction, Myocardial IschemiaArmsColchicine, Placebo oral tablet
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 3 syntheses or guidelines pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Article
  7. Article
  8. Multifaceted roles of neutrophils in cardiac disease.Journal of leukocyte biology · 2025
    Review
  9. Review
  10. Observational
  11. Review
  12. Article
  13. Article
  14. Article
  15. An eNAMPT-neutralizing mAb reduces post-infarct myocardial fibrosis and left ventricular dysfunction.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

2 authors at 2 institutions in 1 country.

Jennifer A RymerDivision of Cardiology, Department of Medicine, and Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.
L Kristin NewbyDivision of Cardiology, Department of Medicine, and Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.
Clinical Research Institute · USDuke University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The importance of inflammation and inflammatory pathways in atherosclerotic disease and acute coronary syndromes (ACS) is well established. The success of statin therapy rests not only on potently reducing levels of low-density lipoprotein cholesterol, but also on the many beneficial, pleiotropic effects statin therapy has on various inflammatory mechanisms in atherosclerotic disease, from reducing endothelial dysfunction to attenuating levels of serum C-reactive protein. Due to the growing awareness of the importance of inflammation in ACS, investigators have attempted to develop novel therapies against known markers of inflammation for several decades. Targeted pathways have ranged from inhibiting C5 cleavage with a high-affinity monoclonal antibody against C5 to inhibiting the activation of the p38 mitogen-activated protein kinase signaling cascades. In each of these instances, despite promising early preclinical and mechanistic studies and phase 2 trials suggesting a potential benefit in reducing post-MI complications or restenosis, these novel therapies have failed to show benefits during large, phase 3 clinical outcomes trials. This review discusses several examples of novel anti-inflammatory therapies that failed to show significant improvement on clinical outcomes when tested in large, randomized trials and highlights potential explanations for why targeted therapies against known markers of inflammation in ACS have failed to launch.

Indexed as

ACS, acute coronary syndromesacute coronary syndromeanti-inflammatoryCABG, coronary artery bypass graftCAD, coronary artery diseasedrug targetsHDL-C, high-density lipoprotein cholesterolhsCRP, high-sensitivity C-reactive proteinIL, interleukinLDL-C, low-density lipoprotein cholesterolLp-PLA2, lipoprotein-associated phospholipase A2MAPK, mitogen-activated protein kinaseMI, myocardial infarctionNSTEMI, non–ST-segment myocardial infarctionPCI, percutaneous coronary interventionPSGL, P-selectin glycoprotein ligandsPLA2, secretory phospholipase A2STEMI, ST-segment elevation myocardial infarctionSVG, saphenous vein graftsTBR, tissue-to-background ratio

Identifiers

PMID30062164
PMCPMC6034453
OpenAlexW2747496024

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.