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Lipoprotein(a) is associated with large artery atherosclerosis stroke aetiology and stroke recurrence among patients below the age of 60 years: Results from the BIOSIGNAL study

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Autor
Arnold M., Schweizer J., Nakas C.T., Schütz V., Westphal L.P., Inauen C., Pokorny T., Luft A., Leichtle A., Arnold M., Bicvic A., Fischer U., De Marchis G.M., Bonati L.H., Müller M.D., Kahles T., Nedeltchev K., Cereda C.W., Kägi G., Bustamante A., Montaner J., Ntaios G., Foerch C., Spanaus K., Von Eckardstein A., Katan M.
Fecha
2021
Language
en
DOI
10.1093/eurheartj/ehab081
Materia
anticoagulant agent
antihypertensive agent
antilipemic agent
antithrombocytic agent
lipoprotein
lipoprotein A
adult
aged
area under the curve
Article
atrial fibrillation
blood clot lysis
brain atherosclerosis
Caucasian
cerebrovascular accident
cohort analysis
controlled study
coronary artery atherosclerosis
demography
disease association
disease classification
disease marker
dyslipidemia
electrocardiography
female
genetic association
human
hypertension
ischemic stroke
limit of detection
limit of quantitation
magnetic resonance angiography
major clinical study
male
mechanical thrombectomy
middle aged
National Institutes of Health Stroke Scale
observational study
receiver operating characteristic
recurrent disease
risk assessment
risk factor
transesophageal echocardiography
transient ischemic attack
very elderly
artery
atherosclerosis
brain ischemia
cerebrovascular accident
clinical trial
complication
multicenter study
prospective study
recurrent disease
Arteries
Atherosclerosis
Brain Ischemia
Cohort Studies
Humans
Lipoprotein(a)
Middle Aged
Prospective Studies
Recurrence
Risk Factors
Stroke
Oxford University Press
Mostrar el registro completo del ítem
Resumen
Aims: Lipoprotein(a) [Lp(a)] is a recognized causal risk factor for atherosclerotic cardiovascular disease but its role for acute ischaemic stroke (AIS) is controversial. In this study, we evaluated the association of Lp(a) with large artery atherosclerosis (LAA) stroke and risk of recurrent cerebrovascular events in AIS patients. Methods and results: For this analysis of the prospective, observational, multicentre BIOSIGNAL cohort study we measured Lp(a) levels in plasma samples of 1733 primarily Caucasian (98.6%) AIS patients, collected within 24 h after symptom onset. Primary outcomes were LAA stroke aetiology and recurrent cerebrovascular events (ischaemic stroke or transient ischaemic attack) within 1 year. We showed that Lp(a) levels are independently associated with LAA stroke aetiology [adjusted odds ratio 1.48, 95% confidence interval (CI) 1.14-1.90, per unit log10Lp(a) increase] and identified age as a potent effect modifier (Pinteraction =0.031) of this association. The adjusted odds ratio for LAA stroke in patients aged <60 years was 3.64 (95% CI 1.76-7.52) per unit log10Lp(a) increase and 4.04 (95% CI 1.73-9.43) using the established cut-off ≥100 nmol/l. For 152 recurrent cerebrovascular events, we did not find a significant association in the whole cohort. However, Lp(a) levels ≥100 nmol/l were associated with an increased risk for recurrent events among patients who were either <60 years [adjusted hazard ratio (HR) 2.40, 95% CI 1.05-5.47], had evident LAA stroke aetiology (adjusted HR 2.18, 95% CI 1.08-4.40), or had no known atrial fibrillation (adjusted HR 1.60, 95% CI 1.03-2.48). Conclusion: Elevated Lp(a) was independently associated with LAA stroke aetiology and risk of recurrent cerebrovascular events among primarily Caucasian individuals aged <60 years or with evident arteriosclerotic disease. © 2021 Published on behalf of the European Society of Cardiology. All rights reserved.
URI
http://hdl.handle.net/11615/70815
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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