Evidence map›Paper›PMID 41792733›Full record

Observational studyLipids in health and disease2026

Lipoprotein(a) and large artery atherosclerosis: results from the BIOSIGNAL study.

Felix Gross, Valerie Schütz, Laura Westphal, Corinne Inauen, Thomas Pokorny, Susanne Wegener, Andreas R Luft, Katharina Spanaus, Arnold von Eckardstein, Pierre-Jean Touboul and 2 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Lipids in health and disease, 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

12 authors.

Felix GrossDepartment of Internal Medicine, Cantonal Hospital of St. Gallen, Rorschacherstrasse 95, St.Gallen, 9007, Switzerland. felix.gross@h-och.ch.
Valerie SchützDepartment of Neurology, University Hospital of Zurich, Zurich, Switzerland.
Laura WestphalDepartment of Neurology, University Hospital of Zurich, Zurich, Switzerland.
Corinne InauenDepartment of Neurology, University Hospital of Zurich, Zurich, Switzerland.
Thomas PokornyDepartment of Neurology, University Hospital of Zurich, Zurich, Switzerland.
Susanne WegenerDepartment of Neurology, University Hospital of Zurich, Zurich, Switzerland.
Andreas R LuftCenter for Neurology and Rehabilitation, Vitznau, Switzerland.
Katharina SpanausDepartment of Neurology, University Hospital of Zurich, Zurich, Switzerland.
Arnold von EckardsteinUniversity of Zurich, Zurich, Switzerland.
Pierre-Jean TouboulStroke Center Bichat Hospital, Paris, France.
Markus Arnold *Department of Neurology, University Hospital of Basel, Basel, Switzerland.
Mira Katan *Department of Neurology, University Hospital of Basel, Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLipoprotein(a) (Lp(a)) is a causal risk-factor for atherosclerotic cardiovascular disease including acute ischemic stroke (AIS). The underlying pathomechanisms mediating this risk are less well understood, especially in AIS caused by large artery atherosclerosis (LAA). In this observational cohort study, we evaluated the association of Lp(a) with markers of LAA, namely carotid intima media thickness (cIMT) and the presence of extra- or intracranial vessel narrowing plaques.

methodsAmong participants of the BIOSIGNAL cohort study we determined Lp(a) levels within 24 h after symptom onset in 1161 AIS patients from the single center of Zurich. cIMT was determined using a semi-automated computerized edge tracking software, internal carotid artery (ICA) stenosis was graded according to the North American Symptomatic Carotid Endarterectomy Trial (NASCET) criteria, intracranial ultrasound was performed by transcranial color-coded duplex (TCCD).

resultsHigher Lp(a) levels were not associated with an increased cIMT in univariable or multivariable regression models containing known cardiovascular risk factors. Higher Lp(a) levels were not associated with the presence of neither extracranial high-grade ICA-stenosis nor significant intracranial stenosis assessed by neurovascular ultrasound.

conclusionIn AIS patients higher Lp(a) levels were not associated with clinical markers of atherosclerotic burden despite its association with LAA-stroke etiology and an increased risk for stroke recurrence.

trial registrationDate of registration: 17–10-2014. Registration-URL: http://www.clinicaltrials.gov ; Unique identifier: NCT-02274727.

Indexed as

AtherosclerosisIschemic StrokeLipoprotein(a)AgedBiomarkersCarotid Artery, InternalCarotid Intima-Media ThicknessCarotid StenosisCohort StudiesFemaleHumansMaleMiddle AgedRisk FactorsBiomarkersLipoprotein(a)Acute ischemic strokeIMTLarge artery atherosclerosisLipoprotein(a)

Identifiers

PMID41792733
PMCPMC13077915

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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 OpenQuestion graph.