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Plaque Regression and Stabilization by Proprotein convertase subtilisin/kexin type 9 Inhibitors: A Meta-Analysis of Intravascular Imaging Studies

Plaque Regression and Stabilization by Proprotein convertase subtilisin/kexin type 9 Inhibitors: A Meta-Analysis of Intravascular Imaging Studies - Plaque Regression and Stabilization by Proprotein convertase subtilisin/kexin type 9 Inhibitors: A Meta-Analysis of Intravascular Imaging Studies

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
JPRN
Registry ID
JPRN-UMIN000058813
Enrollment
Unknown
Registered
2025-08-16
Start date
2025-06-29
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

coronary artery disease (CAD) or acute coronary syndrome (ACS), including unstable angina (UA), non-ST-elevation myocardial infarction (NSTEMI), or ST-elevation myocardial infarction (STEMI)

Interventions

None listed

Sponsors

Dokkyo Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Eligible studies included adult patients with CAD or ACS (UA, NSTEMI, STEMI). Study designs were randomized controlled trials, prospective cohort studies, or retrospective observational studies. The intervention group received PCSK9 inhibitors in addition to statin therapy, and the control group received statin monotherapy or statin plus placebo. Studies were required to assess coronary plaque characteristics at both baseline and follow-up using intravascular imaging modalities (IVUS, OCT, or NIRS). Studies without imaging evaluation or without sufficient data for quantitative synthesis were excluded.

Exclusion criteria

Exclusion criteria: Eligible studies included adult patients with CAD or ACS (UA, NSTEMI, STEMI). Study designs were randomized controlled trials, prospective cohort studies, or retrospective observational studies. The intervention group received PCSK9 inhibitors in addition to statin therapy, and the control group received statin monotherapy or statin plus placebo. Studies were required to assess coronary plaque characteristics at both baseline and follow-up using intravascular imaging modalities (IVUS, OCT, or NIRS). Studies without imaging evaluation or without sufficient data for quantitative synthesis were excluded.

Design outcomes

Primary

MeasureTime frame
The changes in percent atheroma volume (PAV), fibrous cap thickness (FCT), and maximum lipid core burden index within 4 mm (maxLCBI4mm) from baseline to follow-up will be evaluated between the PCSK9 inhibitor group and the control group using an inverse variance random-effects meta-analysis.

Countries

Japan

Contacts

Public ContactRyu Umezono

Dokkyo Medical University Department of Cardiovascular Medicine

umezono.akita587@gmail.com0282872146

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026