Journal article
Coronary artery disease: optimal lipoprotein(a) for survival—lower is better? A large cohort with 43,647 patients
- Abstract:
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Background: A high level of lipoprotein(a) can lead to a high risk of cardiovascular events or mortality. However, the association of moderately elevated lipoprotein(a) levels (≥15 mg/dL) with long-term prognosis among patients with coronary artery disease (CAD) is still uncertain. Hence, we aim to systematically analyzed the relevance of baseline plasma lipoprotein(a) levels to long-term mortality in a large cohort of CAD patients.
Methods: We obtained data from 43,647 patients who were diagnosed with CAD and had follow-up information from January 2007 to December 2018. The patients were divided into two groups (<15 and ≥15 mg/dL). The primary endpoint was long-term all-cause death. Kaplan–Meier curve analysis and Cox proportional hazards models were used to investigate the association between moderately elevated baseline lipoprotein(a) levels (≥15 mg/dL) and long-term all-cause mortality.
Results: During a median follow-up of 5.04 years, 3,941 (18.1%) patients died. We observed a linear association between lipoprotein(a) levels and long-term all-cause mortality. Compared with lipoprotein(a) concentrations <15 mg/dL, lipoprotein(a) ≥15 mg/dL was associated with a significantly higher risk of all-cause mortality [adjusted hazard ratio (aHR) 1.10, 95%CI: 1.04–1.16, P-values = 0.001). Similar results were found for the subgroup analysis of non-acute myocardial infarction, non-percutaneous coronary intervention, chronic heart failure, diabetes mellitus, or non-chronic kidney diseases.
Conclusion: Moderately elevated baseline plasma lipoprotein(a) levels (≥15 mg/dL) are significantly associated with higher all-cause mortality in patients with CAD. Our finding provides a rationale for testing the lipoprotein(a)-reducing hypothesis with lower targets (even <15 mg/dL) in CAD outcome trials.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, 1.3MB, Terms of use)
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- Publisher copy:
- 10.3389/fcvm.2021.670859
Authors
- Publisher:
- Frontiers Media
- Journal:
- Frontiers in Cardiovascular Medicine More from this journal
- Volume:
- 8
- Article number:
- 670859
- Place of publication:
- Switzerland
- Publication date:
- 2021-08-31
- Acceptance date:
- 2021-06-09
- DOI:
- EISSN:
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2297-055X
- Pmid:
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34532348
- Language:
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English
- Keywords:
- Pubs id:
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1194040
- Local pid:
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pubs:1194040
- Deposit date:
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2022-05-24
Terms of use
- Copyright holder:
- Liu et al.
- Copyright date:
- 2021
- Rights statement:
- ©2021 Liu, Liu, Wang, Chen, Liu, Liang, Huang, Li, Lun, Ying, Chen, Huang, Xu, Yan, Zhu, Tadesse, Tan, Chen and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
- Licence:
- CC Attribution (CC BY)
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