Key result
PCS/PoLA cut-offs reduce high-Lp(a) prevalence by ~3 percentage points versus ESC/EAS criteria.
Why the study?
Does applying PCS/PoLA molar cut-offs (75/125 nmol/l) compared to ESC/EAS-based boundaries (62/105 nmol/l) change Lp(a) risk category assignment in adults undergoing routine Lp(a) testing in Poland?
Cross-Sectional (n=23,654)
Yes
Does applying PCS/PoLA molar cut-offs (75/125 nmol/l) compared to ESC/EAS-based boundaries (62/105 nmol/l) change Lp(a) risk category assignment in adults undergoing routine Lp(a) testing in Poland?
Using the higher ≥125 nmol/l cut-off instead of ≥105 nmol/l excludes nearly 1 in 6 patients from the high-Lp(a) risk category despite identical measured concentrations, underscoring the need to interpret Lp(a) continuously within overall cardiovascular risk.
Answers are grounded in this paper and cite their sources.
Lp(a) threshold choice influences prevalence estimates; leaves open outcome-based validation in prospective cohorts.
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Bobrowska et al. (2026) conducted a cross-sectional in Adults undergoing lipoprotein(a) testing for atherosclerotic cardiovascular disease risk assessment (n=23,654). PCS/PoLA categorical thresholds (<75, 75 to <125, ≥125 nmol/l) vs. ESC/EAS-based boundaries (<62, 62 to <105, ≥105 nmol/l) was evaluated on Assignment to the high-Lp(a) concentration category (≥125 vs ≥105 nmol/l) and overall category discordance (4.5%). Applying PCS/PoLA (75/125 nmol/l) versus ESC/EAS (62/105 nmol/l) Lp(a) cut-offs reclassified 4.5% of adults, reducing high-Lp(a) prevalence from 16.2% to 13.6%.
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