Evidence map›Paper›PMID 36599569›Full record

ArticleJACC. Cardiovascular imaging2023

Acute Response in the Noninfarcted Myocardium Predicts Long-Term Major Adverse Cardiac Events After STEMI.

Mayooran Shanmuganathan, Ambra Masi, Matthew K Burrage, Rafail A Kotronias, Alessandra Borlotti, Roberto Scarsini, Abhirup Banerjee, Dimitrios Terentes-Printzios, Qiang Zhang, Evan Hann and 11 more

Abstract read
In one paragraph

Article in JACC. Cardiovascular imaging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Cardiac MRI as Living Histology: Tissue-Based Risk Stratification After STEMI.Journal of magnetic resonance imaging : JMRI · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Management of Myocardial Infarction: Emerging Paradigms for the Future.Methodist DeBakey cardiovascular journal · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Mayooran ShanmuganathanAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Ambra MasiOxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
Matthew K BurrageOxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Rafail A KotroniasAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Alessandra BorlottiAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.
Roberto ScarsiniAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Abhirup BanerjeeAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.
Dimitrios Terentes-PrintziosAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Qiang ZhangOxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
Evan HannOxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
Elizabeth TunnicliffeOxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
Andrew LuckingOxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Jeremy LangrishOxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Rajesh KharbandaOxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Giovanni Luigi De MariaAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Adrian P BanningAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Robin P ChoudhuryAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
Keith M ChannonAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom. Electronic address: keith.channon@cardiov.ox.ac.uk.
Stefan K PiechnikOxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
Vanessa M FerreiraAcute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
OxAMI Study Investigators

Funding

British Heart Foundation CH/16/1/32013British Heart Foundation FS/19/65/34692British Heart Foundation RE/13/1/30181British Heart Foundation RE/18/3/34214Department of Health
6 · The paper itself

Abstract

backgroundAcute ST-segment elevation myocardial infarction (STEMI) has effects on the myocardium beyond the immediate infarcted territory. However, pathophysiologic changes in the noninfarcted myocardium and their prognostic implications remain unclear.

objectivesThe purpose of this study was to evaluate the long-term prognostic value of acute changes in both infarcted and noninfarcted myocardium post-STEMI.

methodsPatients with acute STEMI undergoing primary percutaneous coronary intervention underwent evaluation with blood biomarkers and cardiac magnetic resonance (CMR) at 2 days and 6 months, with long-term follow-up for major adverse cardiac events (MACE). A comprehensive CMR protocol included cine, T2-weighted, T2∗, T1-mapping, and late gadolinium enhancement (LGE) imaging. Areas without LGE were defined as noninfarcted myocardium. MACE was a composite of cardiac death, sustained ventricular arrhythmia, and new-onset heart failure.

resultsTwenty-two of 219 patients (10%) experienced an MACE at a median of 4 years (IQR: 2.5-6.0 years); 152 patients returned for the 6-month visit. High T1 (>1250 ms) in the noninfarcted myocardium was associated with lower left ventricular ejection fraction (LVEF) (51% ± 8% vs 55% ± 9%; P = 0.002) and higher NT-pro-BNP levels (290 pg/L [IQR: 103-523 pg/L] vs 170 pg/L [IQR: 61-312 pg/L]; P = 0.008) at 6 months and a 2.5-fold (IQR: 1.03-6.20) increased risk of MACE (2.53 [IQR: 1.03-6.22]), compared with patients with normal T1 in the noninfarcted myocardium (P = 0.042). A lower T1 (<1,300 ms) in the infarcted myocardium was associated with increased MACE (3.11 [IQR: 1.19-8.13]; P = 0.020). Both noninfarct and infarct T1 were independent predictors of MACE (both P = 0.001) and significantly improved risk prediction beyond LVEF, infarct size, and microvascular obstruction (C-statistic: 0.67 ± 0.07 vs 0.76 ± 0.06, net-reclassification index: 40% [IQR: 12%-64%]; P = 0.007).

conclusionsThe acute responses post-STEMI in both infarcted and noninfarcted myocardium are independent incremental predictors of long-term MACE. These insights may provide new opportunities for treatment and risk stratification in STEMI.

Indexed as

Anterior Wall Myocardial InfarctionPercutaneous Coronary InterventionST Elevation Myocardial InfarctionContrast MediaGadoliniumHumansMagnetic Resonance Imaging, CineMyocardiumPredictive Value of TestsPrognosisStroke VolumeVentricular Function, LeftContrast MediaGadoliniumCMR, heart failureMACEmyocardial injurynoninfarcted myocardiumprognosisSTEMIT1-mapping

Identifiers

PMID36599569
PMCPMC9834063

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.