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. (8th March 2021)

• Record Type: Journal Article
• Authors: Arnold, Markus; Schweizer, Juliane; Nakas, Christos T; Schütz, Valerie; Westphal, Laura P; Inauen, Corinne; Pokorny, Thomas; Luft, Andreas; Leichtle, Alexander; Arnold, Marcel; Bicvic, Antonela; Fischer, Urs; De Marchis, Gian Marco; Bonati, Leo H; Müller, Mandy D; Kahles, Timo; Nedeltchev, Krassen; Cereda, Carlo W; Kägi, Georg; Bustamante, Alejandro; Montaner, Joan; Ntaios, George; Foerch, Christian; Spanaus, Katharina; von Eckardstein, Arnold; Katan, Mira
• Is Part Of: European heart journal. Volume 42:Number 22(2021)
• Page Start: 2186
• Page End: 2196
• Publication Date: 2021-03-08
• Subjects: Lipoprotein(a) -- Acute ischaemic stroke -- Large artery atherosclerosis; Cardiology -- Periodicals; Heart -- Diseases -- Periodicals; 616.12005
• DOI: 10.1093/eurheartj/ehab081
• Languages: English
• ISSNs: 0195-668X

Abstract

Abstract: 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 log10 Lp(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 log10 Lp(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. Graphical Abstract: