Assessing Coronary Non-Culprit Plaque Early with Start of PCSK9 Inhibitors in Acute Myocardial Infarction (ACCESS-AMI)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorYun Dai Chen

About this trial

This study is planned to start on January 2024.

The goal of this clinical trial is to learn whether the perioperative administration (within 24 hours before or after primary PCI) of PCSK9 inhibitors can ameliorate plaque progression and adverse outcomes in patients with acute myocardial infarction (AMI). The main questions it aims to answer are:

Can perioperative PCSK9 inhibition improve the plaque stability and inflammation of perivascular adipose tissue (index of plaque attenuation(IPA )and perivascular fat attenuation index(FAI)) of non-target lesions? Researchers will compare PCSK9 inhibitors with statin plus ezetimibe therapy to evaluate the potential of PCSK9 inhibitors in mitigating the progression of non-target lesion plaques and reducing adverse cardiovascular events in patients with AMI.

Participants will:

Take PCSK9 inhibitors every two weeks or daily statin plus ezetimibe therapy. Conduct a follow-up examination with optical coherence tomography (OCT) or coronary computed tomography angiography (CTA) after 12 months.

Record the occurrence of major adverse cardiovascular events.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years old.

Admitted to hospital for acute myocardial infarction (STEMI, NSTEMI) and successfully underwent PCI of the infarct vessel.

Coronary angiography revealed two non-infarct-related arteries with non-blocking lesions (diameter stenosis of 40-70%).

Able to sign informed consent.

Disqualifiers

Left main artery disease or severe coronary artery calcification;

Hemodynamic instability or uncontrolled arrhythmia;

History of coronary artery bypass;

severe renal insufficiency, active liver disease or liver insufficiency, hematological disease, metabolic or endocrine dysfunction, systemic infection, active malignant tumor and other potentially life-threatening diseases, or the expected survival time is < 1 year;

Trial design

Design model

Parallel

Treatments tested in this trial

  • PCSK9 inhibitor

    Drug

    The patient used Trastuzumab 150mg within 24 hours before or after PCI, and then every two weeks for 12 months

  • Statin+ezetimibe

    Drug

    The patient used statins and ezetimibe within 24 hours before or after PCI, and then once a day for 12 months

  • Blood lipid levels meet the recommended guidelines

    Behavioral

    Early use of intensified lipid-lowering therapy during hospitalization led to a rapid decrease in blood lipids and met the recommended guidelines.

  • Blood lipid levels don't meet the recommended guidelines

    Behavioral

    The patient did not receive intensified lipid-lowering treatment during hospitalization or did not meet the recommended guidelines for blood lipids

Treatment groups

300 Participants
are divided into 2 treatment groups
Group A: PCSK9 inhibitor groupExperimental treatment 2 interventions
Group B: Statin+ezetimibe groupActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Changes in Index of Plaque Attenuation (IPA) measured by OCT for non-culprit lesions at baseline and 12 months of follow-up.

IPA is a quantitative analysis tool based on OCT technology to evaluate plaque stability.

Time frame
12 months
2

Changes in pericoronary artery fat attenuation index (FAI) measured by CCTA for non-culprit lesions at baseline and 12 months of follow-up

FAI is a quantitative indicator of inflammation in perivascular adipose tissue measured by CCTA.

Time frame
12 months

Secondary outcomes

1

Progress of target lesion plaques

To assess plaque progression, OCT evaluation will include fiber cap thickness, lipid core amplitude, minimum lumen area, and minimum lumen diameter. CCTA evaluation will include CAD-RADS grade , plaque volume, plaque properties, calcification score, epicardial fat volume and plaque attenuation. Notes: CAD-RADS indicates Coronary Artery Disease-Reporting and Data System, which range from 0 to 5. The higher CAD-RADS grade, the more severe of the coronary stenosis.

Time frame
12 months
2

The overall incidence of the first major adverse cardiovascular events (MACEs) within 12 months in different treatment groups

MACEs was defined as the composite of myocardial infarction, ischemic stroke, cardiovascular death and coronary revascularization

Time frame
12 months
3

The proportion of LDLC at each visit node that meets the recommended guidelines and the changes compared to baseline

Time frame
1week;1months;3 months; 6 months; 9 months; 12 months
4

Changes in inflammatory factors (interleukin 6, C reaction protein) at each visit node compared to baseline

Time frame
1week;1months;3 months; 6 months; 9 months; 12 months

Other outcomes

Sponsors and contacts

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Yun Dai Chen

Lead sponsor

Chinese PLA General Hospital

Sponsor institution

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