Lipoprotein(a) levels and association with myocardial infarction and stroke in a nationally representative cross-sectional US cohort
- PMID: 32739333
- PMCID: PMC7641964
- DOI: 10.1016/j.jacl.2020.06.010
Lipoprotein(a) levels and association with myocardial infarction and stroke in a nationally representative cross-sectional US cohort
Abstract
Background: Lipoprotein(a) (Lp(a)) has not been well-studied in a nationally representative US cohort.
Objective: The objective of this study was to investigate the distribution of Lp(a) and its associations with nonfatal cardiovascular events in a nationally representative cohort.
Methods: Cross-sectional analysis using the National Health and Nutrition Examination Survey III cohort (1991-1994). We compared Lp(a) levels across demographics and tested the associations between Lp(a) and patient-reported nonfatal myocardial infarction (MI) and/or stroke using multivariate logistic regression.
Results: Median Lp(a) was 14 mg/dL (interquartile range [IQR]: 3, 32) (n = 8214). 14.7% (95% CI: 13.6%-15.9%) had Lp(a) ≥50 mg/dL. Women had slightly higher median Lp(a) than men (14 mg/dL [IQR: 4, 33] vs 13 [(IQR: 3, 30], P = .001). Non-Hispanics blacks had the highest median Lp(a) (35 mg/dL [IQR: 21, 64]), followed by non-Hispanic whites (12 mg/dL [IQR: 3, 29]) and Mexican Americans (8 mg/dL [IQR:1, 21]). In multivariate analysis, Lp(a) was associated (odds ratio per SD increase [95% CI], P-value) with MI (1.41 [1.14-1.75], P = .001), but not stroke (1.14 [0.91-1.44], P = .26). Lp(a) associated with MI in men (1.52 [1.13-2.04], P = .006), non-Hispanic whites (1.60 [1.27-2.03], P < .001), and Mexican Americans (2.14 [1.29-3.55], P = .003), but not women or non-Hispanic blacks. Lp(a) was not associated with stroke among any subgroups.
Conclusion: In a nationally representative US cohort, 1 in 7 had Lp(a) ≥50 mg/dL, the guidelines-recommended threshold to consider Lp(a) a risk enhancing factor. Lp(a) was associated with nonfatal MI but not stroke, although there were differential associations by sex and race/ethnicity. Future nationally representative cohorts should test Lp(a) to get an updated estimation.
Keywords: Cardiovascular disease; Epidemiology; Lipoprotein (a); Myocardial infarction; Risk; Stroke.
Copyright © 2020 National Lipid Association. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Conflicts of interest: Dr Desai reported receiving grants and personal fees from Amgen, Boehringer Ingelheim, and Relypsa; receiving personal fees from Cytokinetics, Novartis, and scPharmaceuticals; having a contract with the Centers for Medicare & Medicaid Services; and receiving funding from Johnson and Johnson and Medtronic outside the submitted work. Dr. Spatz receives support from the Centers for Medicare & Medicaid Services to develop performance measures used in public reporting programs, the Food and Drug Administration to support projects within the Yale-Mayo Clinic Center of Excellence in Regulatory Science and Innovation (CERSI), the National Institute on Minority Health and Health Disparities (U54MD010711–01) to study precision-based approaches to hypertension, and from the National Institute of Biomedical Imaging and Bioengineering (R01 EB028106–01) to study a cuff-less blood pressure device. Dr. Mani receives is supported by grants from the National Institutes of Health (NIH) (RHL135767A). The remaining authors have nothing to disclose.
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