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PCSK9 inhibition

2026 ACC/AHA guideline recommends universal one-time Lp(a) testing, review for endocrinologists on managing elevated levels (J Clin Endocrinol Metab 2026)

Original title: Approach to the Patient with Elevated Lipoprotein(a)

J Clin Endocrinol Metab · · 8

McGinnis T, Saxon DR

Clinical review for endocrinologists on approaching patients with elevated lipoprotein(a) (Lp(a)), a common, genetically determined and independently causal risk factor for myocardial infarction, stroke, peripheral artery disease and calcific aortic stenosis. The 2026 ACC/AHA/Multisociety Dyslipidemia Guideline now recommends one-time Lp(a) measurement in all adults and cascade screening in high-risk families. No approved Lp(a)-specific drug exists yet, so management currently centres on aggressive LDL-C lowering with statins, selective use of PCSK9 inhibitors and lipid apheresis, and possibly aspirin, while antisense oligonucleotide and siRNA therapies that robustly lower Lp(a) are in phase 3 trials. Case-based examples illustrate practical risk assessment and management.

Read the paper (DOI)PubMed

Original abstract

Lipoprotein(a) [Lp(a)] is a common, genetically determined lipoprotein that is independently associated with myocardial infarction, stroke, peripheral artery disease, and calcific aortic stenosis. Because Lp(a) levels are stable over time and minimally influenced by lifestyle, the 2026 ACC/AHA/Multisociety Dyslipidemia Guideline now recommends one-time measurement in all adults and cascade screening in high-risk families; as a result, endocrinologists can expect to encounter and manage elevated Lp(a) frequently in routine clinical practice. Despite its clinical importance, no approved drug therapies specifically targeting Lp(a) yet exist, therefore management should currently focus on aggressive optimization of traditional risk factors, particularly LDL-C lowering with statins and selective use of adjunctive therapies such as PCSK9 inhibitors and lipid apheresis. Emerging evidence suggests potential benefit of selective aspirin use, while novel therapeutics - anti-sense oligonucleotides and small interfering RNAs - which robustly lower Lp(a) are currently being tested in phase 3 clinical trials. We present case-based examples to highlight practical approaches to risk assessment and management of elevated Lp(a).

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Summary written by lp-a.org from the published abstract; figures as published. Page updated 17 August 2026. Methods.