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Prognostic role of lipoprotein(a) in atherosclerotic cardiovascular disease risk from a perspective on current risk stratification.

Authors :
Li S
Liu HH
Zhang Y
Zhang M
Zhang HW
Zhu CG
Wu NQ
Xu RX
Dong Q
Qian J
Dou KF
Guo YL
Li JJ
Source :
MedComm [MedComm (2020)] 2024 Oct 31; Vol. 5 (11), pp. e773. Date of Electronic Publication: 2024 Oct 31 (Print Publication: 2024).
Publication Year :
2024

Abstract

Lipoprotein(a) [Lp(a)] is an emerging predictor for atherosclerotic cardiovascular disease (ASCVD) but the association from a perspective on current risk stratification was unknown. A cohort of 9944 Chinese patients with ASCVD was recruited and refined into very-high-risk (VHR) and non-VHR subgroups according to current guideline. Lp(a) plasma levels were divided by its concentration (<30, 30-50, 50-75, and ≥75 mg/dL) and percentile zones (<25th, 25-50th, 50-75th, 75-90th, ≥90th). Cardiovascular events (CVEs) occurred during an average of 38.5 months' follow-up were recorded. We found that Lp(a) was increased with risk stratification of ASCVD increasing. Prevalence of CVEs had a significantly increasing trend with gradients of Lp(a) elevation in VHR but not in non-VHR subgroup. The adjusted HRs (95%CIs) for CVEs were 1.75(1.25-2.46) in the highest group of Lp(a) ≥75 mg/dL compared with the group of Lp(a) <30 mg/dL as the reference in overall patients, 2.18(1.32-3.58) in VHR subgroup and 1.43(0.93-2.18) in non-VHR subgroup, respectively. The adjusted HRs (95%CIs) at the highest grade of Lp(a) levels (≥90th) were 1.72(1.19-2.50) in overall population, 2.83(1.53-5.24) in VHR subgroup and 1.38(0.86-2.12) in non-VHR subgroup, respectively. These findings suggested that Lp(a) might contribute more to CVEs risk in VHR subgroup of ASCVD.<br />Competing Interests: The authors declare that there is no conflict of interest.<br /> (© 2024 The Author(s). MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd.)

Details

Language :
English
ISSN :
2688-2663
Volume :
5
Issue :
11
Database :
MEDLINE
Journal :
MedComm
Publication Type :
Academic Journal
Accession number :
39492837
Full Text :
https://doi.org/10.1002/mco2.773