Lipoprotein(a) as a blood marker for large artery atherosclerosis stroke etiology: validation in a prospective cohort from a swiss stroke center.

Rudin, Salome; Kriemler, Lilian; Dittrich, Tolga D; Zietz, Annaelle; Schweizer, Juliane; Arnold, Markus; Peters, Nils; Barinka, Filip; Jung, Simon; Arnold, Marcel; Fischer, Urs; Rentsch, Katharina; Christ-Crain, Mirjam; Katan, Mira; De Marchis, Gian Marco (2024). Lipoprotein(a) as a blood marker for large artery atherosclerosis stroke etiology: validation in a prospective cohort from a swiss stroke center. Swiss medical weekly, 154(4) SMW supporting association 10.57187/s.3633

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BACKGROUND

Lipoprotein (a) [Lp(a)] serum levels are highly genetically determined and promote atherogenesis. High Lp(a) levels are associated with increased cardiovascular morbidity. Serum Lp(a) levels have recently been associated with large artery atherosclerosis (LAA) stroke. We aimed to externally validate this association in an independent cohort.

METHODS

This study stems from the prospective multicentre CoRisk study (CoPeptin for Risk Stratification in Acute Stroke patients [NCT00878813]), conducted at the University Hospital Bern, Switzerland, between 2009 and 2011, in which Lp(a) plasma levels were measured within the first 24 hours after stroke onset. We assessed the association of Lp(a) with LAA stroke using multivariable logistic regression and performed interaction analyses to identify potential effect modifiers.

RESULTS

Of 743 patients with ischaemic stroke, 105 (14%) had LAA stroke aetiology. Lp(a) levels were higher for LAA stroke than non-LAA stroke patients (23.0 nmol/l vs 16.3 nmol/l, p = 0.01). Multivariable regression revealed an independent association of log10and#xA0;Lp(a) with LAA stroke aetiology (aOR 1.47 [95% CI 1.03and#x2013;2.09], p = 0.03). The interaction analyses showed that Lp(a) was not associated with LAA stroke aetiology among patients with diabetes.

CONCLUSIONS

In a well-characterised cohort of patients with ischaemic stroke, we validated the association of higher Lp(a) levels with LAA stroke aetiology, independent of traditional cardiovascular risk factors. These findings may inform randomised clinical trials investigating the effect of Lp(a) lowering agents on cardiovascular outcomes. The CoRisk (CoPeptin for Risk Stratification in Acute Patients) study is registered on ClinicalTrials.gov.

REGISTRATION NUMBER

NCT00878813.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Neurology

UniBE Contributor:

Jung, Simon, Arnold, Marcel, Fischer, Urs Martin

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1424-3997

Publisher:

SMW supporting association

Language:

English

Submitter:

Pubmed Import

Date Deposited:

09 Apr 2024 13:53

Last Modified:

09 Apr 2024 14:02

Publisher DOI:

10.57187/s.3633

PubMed ID:

38579294

BORIS DOI:

10.48350/195718

URI:

https://boris.unibe.ch/id/eprint/195718

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