Lipoprotein (a) and cerebrovascular disease

Author:

Kosmas Constantine E.1ORCID,Bousvarou Maria D.2,Papakonstantinou Evangelia J.3,Zoumi Eleni-Angeliki4,Rallidis Loukianos S.1

Affiliation:

1. 2nd Department of Cardiology, National & Kapodistrian University of Athens, Athens, Greece

2. School of Medicine, University of Crete, Heraklion, Greece

3. General Directorate of Public Health and Social Welfare, Attica Region, Athens, Greece

4. University of Exeter Medical School, Exeter, Devon, United Kingdom

Abstract

The role of lipoprotein (a) [Lp(a)] in cerebrovascular disease is a topic of importance. In this narrative review, pertinent studies have been leveraged to comprehensively examine this relationship from diverse perspectives. Lp(a) shares structural traits with low-density lipoprotein cholesterol. Lp(a) is synthesized by hepatocytes, and its plasma levels are genetically determined by the LPA gene, which produces apolipoprotein (a). Numerous epidemiological studies have confirmed the positive correlation between elevated serum Lp(a) levels and the occurrence or recurrence of cerebrovascular events, especially ischemic strokes, in adults. It should be noted that the correlation strength varies among studies and is marginal in Mendelian randomization studies. Regarding pediatric patients, screening is currently limited to those with a relevant medical history. Lp(a) seems to play a significant role in the pathogenesis of arterial ischemic stroke in children because environmental thrombotic and atherogenic factors are generally not present. Phase 3 trials of novel Lp(a) targeting agents, such as pelacarsen and olpasiran, are anticipated to demonstrate their efficacy in reducing the incidence of stroke. Given the richness of the literature, new guidelines regarding Lp(a) screening and management in targeted populations are warranted to provide more effective primary and secondary prevention.

Publisher

SAGE Publications

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