Evidence map›Paper›PMID 42714476›Full record

Trial reportJournal of the American Heart Association2026

Add-On PCSK9 Inhibitor Therapy for Acute Stroke Attributable to Intracranial Atherosclerosis: A Randomized Clinical Trial.

Yi-Ting Pan, Yuan-Hsiung Tsai, Hsu-Huei Weng, Jiann-Der Lee, Jen-Tsung Yang, Leng-Chieh Lin, Yen-Chu Huang

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT05001984. 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.

NCT05001984 phase2active not recruiting

Trial of PCSK9 Inhibition in Patients with Acute Stroke and Symptomatic Intracranial Atherosclerosis - a Prospective, Randomized, Open-label, Blinded End-point Study with High-resolution MR Vessel Wall Imaging

Ran2021Enrolled60Registered outcomes11Posted comparisons0ConditionsAcute Ischemic Stroke, ICAS - Intracranial Atherosclerosis, Intracranial AtherosclerosisArmsAlirocumab
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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

7 authors.

Yi-Ting PanDepartment of Neurology Chang Gung Memorial Hospital at Chiayi, Chang-Gung University College of Medicine Taoyuan City Taiwan.ORCID 0000-0003-2485-4783
Yuan-Hsiung TsaiDepartment of Diagnostic Radiology Chang Gung Memorial Hospital at Chiayi, Chang-Gung University College of Medicine Taoyuan City Taiwan.ORCID 0000-0003-4906-0365
Hsu-Huei WengDepartment of Diagnostic Radiology Chang Gung Memorial Hospital at Chiayi, Chang-Gung University College of Medicine Taoyuan City Taiwan.ORCID 0000-0002-2020-8912
Jiann-Der LeeDepartment of Neurology Chang Gung Memorial Hospital at Chiayi, Chang-Gung University College of Medicine Taoyuan City Taiwan.
Jen-Tsung YangDepartment of Neurosurgery Chang Gung Memorial Hospital at Chiayi, Chang-Gung University College of Medicine Taoyuan City Taiwan.
Leng-Chieh LinDepartment of Emergency Medicine Chang Gung Memorial Hospital at Chiayi, Chang-Gung University College of Medicine Taoyuan City Taiwan.ORCID 0000-0001-6524-2324
Yen-Chu HuangDepartment of Neurology Chang Gung Memorial Hospital at Chiayi, Chang-Gung University College of Medicine Taoyuan City Taiwan.ORCID 0000-0001-7885-6376

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntracranial atherosclerotic stenosis is a major cause of ischemic stroke with high recurrence rates despite intensive therapy. The efficacy of proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) as adjunctive treatment in intracranial atherosclerotic stenosis remains unclear.

methodsWe conducted a prospective, randomized, open-label, blinded-end point trial involving 62 patients with symptomatic intracranial atherosclerotic stenosis. Participants were randomized 1:2 to receive either a PCSK9i (alirocumab 75 mg every 2 weeks) plus high-intensity statin or high-intensity statin alone for 6 months. The primary outcome was the change in intracranial artery stenosis measured by high-resolution vessel-wall magnetic resonance imaging. Secondary outcomes included plaque enhancement volume, low-density lipoprotein cholesterol target achievement (<55 mg/dL), recurrent stroke events, modified Rankin Scale, and safety assessments.

resultsAmong 62 participants (median age, 66 years; 77% men), 60 completed the study per protocol. At 6 months, median stenosis reduction was greater in the PCSK9i group (7.1%; interquartile range, 3.6-12.8%) than in controls (-1.2%; interquartile range, -4.9-4.5%) (

conclusionsIn patients with symptomatic intracranial atherosclerotic stenosis, adjunctive PCSK9i therapy significantly reduced intracranial stenosis and improved low-density lipoprotein cholesterol control over 6 months. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique Identifier: NCT05001984.

Indexed as

Antibodies, Monoclonal, HumanizedAnticholesteremic AgentsHydroxymethylglutaryl-CoA Reductase InhibitorsIntracranial ArteriosclerosisIschemic StrokePCSK9 InhibitorsStrokeAgedCholesterol, LDLConstriction, PathologicDrug Therapy, CombinationFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedalirocumabAntibodies, Monoclonal, HumanizedAnticholesteremic AgentsCholesterol, LDLHydroxymethylglutaryl-CoA Reductase InhibitorsPCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9alirocumabintracranial atherosclerotic stenosisMRIPCSK9 inhibitor

Identifiers

PMID42714476
PMCPMC13744962

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Registered trials

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 OpenQuestion graph.