Lipoprotein(a) and Atrial Fibrillation: A Systematic Review and Meta-Analysis
Authors:
- Bartosz MajBMBartosz Maj
- Michal PrucMPMichal Pruc
- Pawel CzubakPCPawel Czubak
- Iga RomanskaIRIga Romanska
- Karol MomotKMKarol Momot
- Marta KlosMKMarta Klos
- Kamil KrauzKKKamil Krauz
- Aleksandra MielnikAMAleksandra Mielnik
- Zbigniew SiudakZbigniew Siudak
- Katarzyna KotfisKKKatarzyna Kotfis
- Lukasz SzarpakLukasz Szarpak
Open Access
- 1 November 2025
- journal article
- review article
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 14 (21) , 7770
Abstract
Background/Objectives: The most prevalent prolonged cardiac arrhythmia and a significant global health burden is atrial fibrillation (AF). Although its connection to AF is still unknown, lipoprotein(a) (Lp(a)), a genetically determined lipoprotein with pro-inflammatory and pro-atherogenic characteristics, has been linked to cardiovascular disease. The purpose of this study was to measure and assess the relationship between circulating Lp(a) levels and AF. Methods: In compliance with the PRISMA 2020 guidelines, a systematic review and meta-analysis were carried out using a protocol that was preregistered in PROSPERO (CRD420251153244). Comprehensive searches of PubMed/MEDLINE, Embase, Web of Science, Scopus, the Cochrane Library, and Google Scholar up until September 2025 were used to find observational studies comparing circulating Lp(a) levels in adults with and without AF. Results: Circulating Lp(a) concentrations were significantly higher in AF patients than in controls across 10 studies (pooled MD = 2.81; 95%CI: 1.58–4.05; p < 0.0001). In the subgroup analysis by geographical setting, studies conducted in Asia and studies from Europe/USA exhibited a statistically significant effect. Despite the extreme heterogeneity (I2 = 99%), sensitivity analyses verified that the overall effect was stable. Conclusions: Our pooled analysis revealed a statistically significant association between Lp(a) and AF; however, the certainty of the evidence was rated as very low according to the GRADE methodology. To elucidate causality, enhance risk stratification, and investigate whether Lp(a)-lowering tactics could alter AF risk, large, prospective, multi-ethnic studies with standardized biomarker assessment are needed.Keywords
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