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Updated: Jan 31, 2026

Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
Reduction in Subtypes and Sizes of Myocardial Infarction With Ticagrelor in PEGASUS-TIMI 54
Marc P Bonaca1, Stephen D Wiviott1, David A Morrow1
11 TIMI Study Group Brigham and Women's Hospital Boston MA.
Insights
Ticagrelor effectively reduced myocardial infarction (MI) in patients with prior MI. The drug demonstrated consistent benefits across various MI subtypes and sizes, including large and ST-elevation MIs.
Area of Science:
- Cardiology
- Clinical Trials
- Pharmacology
Background:
- Ticagrelor demonstrated efficacy in reducing cardiovascular events in patients with prior myocardial infarction (MI) in the PEGASUS-TIMI 54 trial.
- Understanding the specific types and severity of MI events prevented by ticagrelor is crucial for clinical practice.
Purpose of the Study:
- To analyze the types and sizes of myocardial infarction (MI) events reduced by ticagrelor in patients with a history of MI.
- To assess the consistency of ticagrelor's benefit across different MI subtypes and biomarker elevations.
Main Methods:
- Myocardial infarction (MI) events were adjudicated by a blinded clinical events committee.
- MIs were categorized by subtype (e.g., spontaneous, demand, stent thrombosis) and peak cardiac troponin elevation.
- Data from the PEGASUS-TIMI 54 trial, involving 21,162 patients, were analyzed over a median follow-up of 33 months.
Main Results:
- A total of 1042 MIs occurred, with 76% being spontaneous (Type 1).
- Half of MIs had peak troponin ≥10x the upper limit of normal, and 21% had peak troponin ≥100x.
- Ticagrelor significantly reduced MI events (HR 0.83, P=0.0055), with notable reductions in large MIs (peak troponin ≥100x; HR 0.69, P=0.0096) and ST-segment elevation MI (STEMI; HR 0.60, P=0.0002).
Conclusions:
- In stable outpatients with prior MI, recurrent MIs are predominantly spontaneous and associated with high biomarker elevations.
- Ticagrelor consistently reduces MI events across various subtypes and sizes, including large MIs and STEMI.
- These findings underscore the broad protective effect of ticagrelor in high-risk cardiovascular patients.
Abstract:
Background Ticagrelor reduced cardiovascular death, myocardial infarction (MI), or stroke in patients with prior MI in PEGASUS-TIMI 54 (Prevention of Cardiovascular Events [eg, Death From Heart or Vascular Disease, Heart Attack, or Stroke] in Patients With Prior Heart Attack Using Ticagrelor Compared to Placebo on a Background of Aspirin). MI can occur in diverse settings and with varying severity; therefore, understanding the types and sizes of MI events prevented is of clinical importance. Methods and Results MIs were adjudicated by a blinded clinical events committee and categorized by subtype and fold elevation of peak cardiac troponin over the upper limit of normal. A total of 1042 MIs occurred in 898 of the 21 162 randomized patients over a median follow-up of 33 months. The majority of the MIs (76%) were spontaneous (Type 1), with demand MI (Type 2) and stent thrombosis (Type 4b) accounting for 13% and 9%, respectively; sudden death (Type 3), percutaneous coronary intervention-related (Type 4a) and coronary artery bypass graft-related (Type 5) each accounted for <1%. Half of MIs (520, 50%) had a peak troponin ≥10x upper limit of normal and 21% of MIs (220) had a peak troponin ≥100× upper limit of normal. A total of 21% (224) were ST-segment-elevation MI STEMI. Overall ticagrelor reduced MI (4.47% versus 5.25%, hazard ratio 0.83, 95% confidence interval 0.72-0.95, P=0.0055). The benefit was consistent among the subtypes, including a 31% reduction in MIs with a peak troponin ≥100× upper limit of normal (hazard ratio 0.69, 95% confidence interval 0.53-0.92, P=0.0096) and a 40% reduction in ST-segment elevation MI (hazard ratio 0.60, 95% confidence interval 0.46-0.78, P=0.0002). Conclusions In stable outpatients with prior MI, the majority of recurrent MIs are spontaneous and associated with a high biomarker elevation. Ticagrelor reduces the MI consistently among subtypes and sizes including large MIs and ST-segment elevation MI. Clinical Trial Registration URL: https://www.clinicaltrials.gov . Unique identifier: NCT01225562.
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