Evidence map›Paper›PMID 41400669›Full record

ArticleClinical research in cardiology : official journal of the German Cardiac Society2026

Prognostic value of lipoprotein(a) in a primary prevention ambulatory cohort.

Netanel Golan, Ophir Freund, Tamar Itach, Yaron Arbel

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Article in Clinical research in cardiology : official journal of the German Cardiac Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Netanel GolanDivision of Cardiology, Faculty of Medical & Health Sciences, Tel-Aviv Sourasky Medical Center, Tel Aviv University, 6 Weizman Street, Tel Aviv, Israel.
Ophir FreundInstitute of Pulmonary Medicine, Faculty of Medical & Health Sciences, Tel Aviv Sourasky Medical Center, Tel Aviv University, Tel Aviv, Israel.
Tamar ItachDivision of Cardiology, Faculty of Medical & Health Sciences, Tel-Aviv Sourasky Medical Center, Tel Aviv University, 6 Weizman Street, Tel Aviv, Israel.
Yaron ArbelDivision of Cardiology, Faculty of Medical & Health Sciences, Tel-Aviv Sourasky Medical Center, Tel Aviv University, 6 Weizman Street, Tel Aviv, Israel. yarona@tlvmc.gov.il.ORCID http://orcid.org/0000-0003-4258-6313

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsLipoprotein(a) [Lp(a)] is a novel biomarker for Atherosclerotic cardiovascular disease prediction. Yet, given the scarcity in high-quality evidence, its use in routine primary prevention screening is lacking. For this reason, we aimed to assess Lp(a) prognostic utility during routine screening.

methodsA retrospective cohort of adults with available Lp(a) measurement, taken during a screening program (2008-2024) in a tertiary care center. Major adverse cardiovascular events (MACE) was the study primary outcome. The optimal Lp(a) threshold was evaluated using spline curve analysis and validated by Cox regression models adjusted for clinical and laboratory covariates. Subgroup analyses were performed in patients with SCORE2 and PCE data.

results3052 people were included with a median (IQR) follow-up of 6.4 (3.5-12) years. Lp(a) threshold of 50 mg/dL was identified as a risk inflection point. High Lp(a) (> 50 mg/dL) was associated with increased MACE risk, independent of clinical data (HR 1.55, 95% CI 1.10-2.17, p = 0.011) or different laboratory variables (HR 1.62, 95% CI 1.07-2.46). High Lp(a) remained a predictor for MACE in models incorporating the SCORE2 and PCE scores, and its incorporation into these scores improved their performance in high-risk patients. In people with cardiovascular comorbidities, the optimal Lp(a) threshold for MACE prediction was 61 mg/dL, while it was 48.4 mg/dL in those without (n = 2778).

conclusionsIn a large ambulatory and mostly healthy cohort, Lp(a) showed a strong predictive utility for cardiovascular events. These findings support the integration of Lp(a) into primary cardiovascular risk assessment and role in guiding emerging targeted therapies.

Indexed as

Cardiovascular DiseasesLipoprotein(a)Mass ScreeningPrimary PreventionAdultAgedBiomarkersFemaleFollow-Up StudiesHumansMaleMiddle AgedPredictive Value of TestsPrognosisRetrospective StudiesRisk AssessmentBiomarkersLipoprotein(a)ASCVD risk model (PCE)Atherosclerotic cardiovascular diseaseCardiovascular risk assessmentLipoprotein(a)Primary preventionSCORE2

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.