Coronary Atherosclerotic Plaque Activity and Future Coronary Events

Author:

Moss Alastair123,Daghem Marwa12,Tzolos Evangelos12,Meah Mohammed N.12,Wang Kang-Ling12,Bularga Anda12,Adamson Philip D.4,Kwiecinski Jacek5,Fletcher Alison12,Dawson Dana6,Arumugam Parthiban7,Sabharwal Nikant8,Greenwood John P.9,Townend Jon N.10,Calvert Patrick A.11,Rudd James H. F.12,Berman Dan13,Verjans Johan14,Slomka Piotr13,Dey Damini13,Forsyth Laura15,Murdoch Lauren15,Lee Robert J.15,Lewis Steff15,Mills Nicholas L.1216,van Beek Edwin J. R.12,Williams Michelle C.12,Dweck Marc R.12,Newby David E.12,Briola Anny17,Armstrong Ruth17,Macdonald Alix17,Scott Gill17,Milne Garry17,Milne Lynsey17,Battison Claire17,Wilkins Martin R17,Storey Robert F17,Razavi Reza17,Wallberg Maja17,Mycock Rodney17,

Affiliation:

1. Edinburgh Imaging, The University of Edinburgh, Edinburgh, Scotland

2. British Heart Foundation Centre for Cardiovascular Science, The University of Edinburgh, Edinburgh, Scotland

3. National Institute for Health and Care Research, Leicester Biomedical Research Centre, University of Leicester, Leicester, England

4. Christchurch Heart Institute, University of Otago, Christchurch, New Zealand

5. Department of Interventional Cardiology and Angiology, Institute of Cardiology, Warsaw, Poland

6. Aberdeen Cardiovascular and Diabetes Centre, University of Aberdeen, Aberdeen, Scotland

7. Manchester University, NHS Foundation Trust, Manchester, England

8. Oxford University Hospitals, NHS Foundation Trust, Oxford, England

9. Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, England

10. Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, England

11. Royal Papworth Hospital, University of Cambridge, Cambridge, England

12. Department of Medicine, University of Cambridge, Cambridge, England

13. Cedars-Sinai Medical Center, Los Angeles, California

14. Adelaide Medical School, The University of Adelaide, Adelaide, Australia

15. Edinburgh Clinical Trials Unit, Usher Institute, The University of Edinburgh, Edinburgh, Scotland

16. Usher Institute, The University of Edinburgh, Edinburgh, Scotland

17. for the PREFFIR Investigators

Abstract

ImportanceRecurrent coronary events in patients with recent myocardial infarction remain a major clinical problem. Noninvasive measures of coronary atherosclerotic disease activity have the potential to identify individuals at greatest risk.ObjectiveTo assess whether coronary atherosclerotic plaque activity as assessed by noninvasive imaging is associated with recurrent coronary events in patients with myocardial infarction.Design, Setting, and ParticipantsThis prospective, longitudinal, international multicenter cohort study recruited participants aged 50 years or older with multivessel coronary artery disease and recent (within 21 days) myocardial infarction between September 2015 and February 2020, with a minimum 2 years’ follow-up.InterventionCoronary 18F-sodium fluoride positron emission tomography and coronary computed tomography angiography.Main Outcomes and MeasuresTotal coronary atherosclerotic plaque activity was assessed by 18F-sodium fluoride uptake. The primary end point was cardiac death or nonfatal myocardial infarction but was expanded during study conduct to include unscheduled coronary revascularization due to lower than anticipated primary event rates.ResultsAmong 2684 patients screened, 995 were eligible, 712 attended for imaging, and 704 completed an interpretable scan and comprised the study population. The mean (SD) age of participants was 63.8 (8.2) years, and most were male (601 [85%]). Total coronary atherosclerotic plaque activity was identified in 421 participants (60%). After a median follow-up of 4 years (IQR, 3-5 years), 141 participants (20%) experienced the primary end point: 9 had cardiac death, 49 had nonfatal myocardial infarction, and 83 had unscheduled coronary revascularizations. Increased coronary plaque activity was not associated with the primary end point (hazard ratio [HR], 1.25; 95% CI, 0.89-1.76; P = .20) or unscheduled revascularization (HR, 0.98; 95% CI, 0.64-1.49; P = .91) but was associated with the secondary end point of cardiac death or nonfatal myocardial infarction (47 of 421 patients with high plaque activity [11.2%] vs 19 of 283 with low plaque activity [6.7%]; HR, 1.82; 95% CI, 1.07-3.10; P = .03) and all-cause mortality (30 of 421 patients with high plaque activity [7.1%] vs 9 of 283 with low plaque activity [3.2%]; HR, 2.43; 95% CI, 1.15-5.12; P = .02). After adjustment for differences in baseline clinical characteristics, coronary angiography findings, and Global Registry of Acute Coronary Events score, high coronary plaque activity was associated with cardiac death or nonfatal myocardial infarction (HR, 1.76; 95% CI, 1.00-3.10; P = .05) but not with all-cause mortality (HR, 2.01; 95% CI, 0.90-4.49; P = .09).Conclusions and RelevanceIn this cohort study of patients with recent myocardial infarction, coronary atherosclerotic plaque activity was not associated with the primary composite end point. The findings suggest that risk of cardiovascular death or myocardial infarction in patients with elevated plaque activity warrants further research to explore its incremental prognostic implications.

Publisher

American Medical Association (AMA)

Subject

Cardiology and Cardiovascular Medicine

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