Evidence map›Paper›PMID 41923749›Full record

SynthesisReviews in cardiovascular medicine2026

Proprotein Convertase Subtilisin/Kexin Type 9 and Atherosclerotic Plaque Progression: A Systematic Review and Meta-Analysis of Intravascular Imaging Studies.

Panagiotis Theofilis, Panayotis K Vlachakis, Paschalis Karakasis, Panagiotis Iliakis, Konstantinos Pamporis, Evangelos Oikonomou, Kyriakos Dimitriadis, Konstantinos Tsioufis, Dimitris Tousoulis

Abstract readSystematic Review
In one paragraph

Synthesis in Reviews in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Panagiotis TheofilisCardiology Department, "Hippokration" General Hospital, University of Athens Medical School, 11527 Athens, Greece.ORCID https://orcid.org/0000-0001-9260-6306
Panayotis K VlachakisCardiology Department, "Hippokration" General Hospital, University of Athens Medical School, 11527 Athens, Greece.ORCID https://orcid.org/0000-0003-0736-4942
Paschalis KarakasisCardiology Department, "Hippokration" General Hospital, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece.ORCID https://orcid.org/0000-0002-3561-5713
Panagiotis IliakisCardiology Department, "Hippokration" General Hospital, University of Athens Medical School, 11527 Athens, Greece.ORCID https://orcid.org/0009-0004-5768-9125
Konstantinos PamporisCardiology Department, "Hippokration" General Hospital, University of Athens Medical School, 11527 Athens, Greece.ORCID https://orcid.org/0000-0001-5411-6461
Evangelos OikonomouCardiology Department, "Sotiria" Regional Hospital for Chest Diseases, University of Athens Medical School, 11527 Athens, Greece.ORCID https://orcid.org/0000-0001-8079-0599
Kyriakos DimitriadisCardiology Department, "Hippokration" General Hospital, University of Athens Medical School, 11527 Athens, Greece.ORCID https://orcid.org/0000-0003-3186-8905
Konstantinos TsioufisCardiology Department, "Hippokration" General Hospital, University of Athens Medical School, 11527 Athens, Greece.ORCID https://orcid.org/0000-0002-7636-6725
Dimitris TousoulisCardiology Department, "Hippokration" General Hospital, University of Athens Medical School, 11527 Athens, Greece.ORCID https://orcid.org/0000-0001-7492-4984

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9is) have emerged as a promising class of medications, primarily recognized for inducing potent cholesterol-lowering effects. In addition to the established role of these inhibitors in reducing low-density lipoprotein cholesterol levels, recent studies suggest that PCSK9is may also modify coronary atherosclerotic plaques. Therefore, this meta-analysis aimed to comprehensively synthesize data from relevant clinical studies and trials investigating the effects of PCSK9is on coronary atherosclerotic plaque characteristics. Methods: We performed a literature search for studies assessing the evolution of coronary atherosclerotic plaques after treatment with a PCSK9i compared with a control group. We excluded reviews, editorials, case reports/case series, and studies that did not use PCSK9is or lacked a control group. The main outcomes of interest were changes in percent atheroma volume (PAV), total atheroma volume (TAV), minimal fibrous cap thickness (FCT), lipid arc, and the number of patients with improved PAVs at follow-up. Effect sizes are presented as a standardized mean difference (SMD) or risk ratio (RR) alongside the corresponding 95% confidence intervals (CIs) and were pooled based on a random-effects model. Publication bias was assessed by funnel plot inspection and Egger's regression test. Results: The literature search yielded 142 results. After applying the exclusion criteria, nine studies were selected for data extraction and inclusion in the meta-analysis. Concerning the intravascular ultrasound findings, PCSK9is significantly reduced the TAV (MD -7.09 mm Conclusions: This meta-analysis suggests that PCSK9i therapy may be associated with modest favorable changes in selected intravascular imaging markers of coronary atherosclerotic plaque burden and stability.

Indexed as

atheroma volumeatherosclerosiscoronary artery diseasefibrous cap thicknesslipid arcPCSK9 inhibitor

Identifiers

PMID41923749
PMCPMC13036525

What Socratic holds

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Registered trials

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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 Socratic graph.