Key result
PCSK9 inhibitor added to high-intensity statin manages premature CAD with markedly elevated Lp(a).
Case Report (n=1)
This case highlights the clinical importance of routinely measuring Lipoprotein(a) for risk stratification in patients with early cardiovascular disease and a family history of premature events.
Lipoprotein(a) (Lp(a)) is increasingly recognized as a significant contributor to the risk of atherosclerotic cardiovascular disease (ASCVD). We report the case of a 53-year-old woman who presented with chest pain and has notable family history of premature cardiovascular events. Investigation revealed a markedly elevated Lp(a) level of 492 nmol/L, alongside the presence of coronary artery disease necessitating stenting. Despite adherence to high-intensity statin therapy, her low-density lipoprotein (LDL) cholesterol levels remained suboptimal. Consequently, we initiated treatment with a PCSK9 inhibitor to achieve further reductions in LDL cholesterol. This case underscores the importance of routinely measuring Lp(a), as recommended by European guidelines, which advocate for its assessment at least once during adulthood for effective risk stratification. While lifestyle interventions play a critical role in cardiovascular health, targeted therapies such as PCSK9 inhibitors and emerging nucleic acid-based treatments, including Zerlasiran, offer promising options for significantly lowering Lp(a) levels. Recognizing and addressing elevated Lp(a) is vital for identifying patients at high cardiovascular risk and for informing tailored management strategies aimed at improving patient outcomes.
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Abdelgadir et al. (2026) conducted a case report in Early cardiovascular disease (n=1). Elevated Lipoprotein(a) was evaluated. Markedly elevated Lipoprotein(a) (492 nmol/L) was identified in a 53-year-old woman presenting with chest pain and premature cardiovascular family history, who required coronary stenting.
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