Prevalence and Correlates of Lipoprotein(a) Testing in a Diverse Cohort of U.S. Adults
- PMID: 40570403
- PMCID: PMC12164155
- DOI: 10.1016/j.jacadv.2025.101826
Prevalence and Correlates of Lipoprotein(a) Testing in a Diverse Cohort of U.S. Adults
Abstract
Background: Once-per-lifetime lipoprotein(a) [Lp(a)] testing is recommended by multiple professional societies during cardiovascular disease risk assessment.
Objective: The purpose of this study was to assess the prevalence and identify correlates of Lp(a) testing in a real-world, diverse sample.
Methods: Participants were ≥18 years of age from the All of Us Research Study who shared electronic medical record information through 2022 (N = 266,612). Completion of Lp(a) testing was defined by the following: presence of Lp(a) values, Systematized Nomenclature of Medicine Clinical Terms or Logical Observation Identifiers Names and Codes electronic health record listings for Lp(a) testing, or an Internal Classification of Diseases-10 code for elevated Lp(a). Multivariable logistic regression assessed the association of demographic, socioeconomic, and clinical variables with Lp(a) testing.
Results: The mean age was 52 years, 61% were women, and 53% were non-Hispanic White. A total of 2,172 (0.8%) underwent Lp(a) testing, 86% of whom had clinical cardiovascular disease. Compared to non-Hispanic White individuals, non-Hispanic Black individuals (OR: 0.68, 95% CI: 0.58-0.81) had 32% lower odds of Lp(a) testing. Less than high school education (OR: 0.34, 95% CI: 0.25-0.44), unemployment (OR: 0.76, 95% CI: 0.68-0.85), and disability (OR: 0.77, 95% CI: 0.65-0.91) were associated with a 23% to 66% lower odds of Lp(a) testing. Among clinical factors, non-Lp(a) lipid abnormality (OR: 5.64, 95% CI: 4.72-6.79) and prevalent cardiovascular disease (OR: 3.21, 95% CI: 2.76-3.74) were strongly associated with Lp(a) testing.
Conclusions: The prevalence of Lp(a) testing among US adults is exceedingly low, especially for non-Hispanic Black individuals and those with socioeconomic risk. These results underline the importance of emphasizing health equity in Lp(a) testing expansion.
Keywords: cardiovascular disease; lipoprotein(a); preventive cardiology; risk assessment; risk factor; testing.
Copyright © 2025 The Authors. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Funding support and author disclosures Bhatia reports consulting fees from Abbott, Arrowhead, Kaneka, and Novartis and is supported by National Institutes of Health, Grant 1K08HL166962. Razavi is supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health, Grants F32HL172499 and L30HL175751. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
Figures



Similar articles
-
Signs and symptoms to determine if a patient presenting in primary care or hospital outpatient settings has COVID-19.Cochrane Database Syst Rev. 2022 May 20;5(5):CD013665. doi: 10.1002/14651858.CD013665.pub3. Cochrane Database Syst Rev. 2022. PMID: 35593186 Free PMC article.
-
Factors Associated with Lipoprotein(a) Testing Among Multiethnic Individuals.J Gen Intern Med. 2025 Mar;40(4):756-763. doi: 10.1007/s11606-024-09126-6. Epub 2024 Oct 25. J Gen Intern Med. 2025. PMID: 39455482
-
Surveillance for Violent Deaths - National Violent Death Reporting System, 50 States, the District of Columbia, and Puerto Rico, 2022.MMWR Surveill Summ. 2025 Jun 12;74(5):1-42. doi: 10.15585/mmwr.ss7405a1. MMWR Surveill Summ. 2025. PMID: 40493548 Free PMC article.
-
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.Cochrane Database Syst Rev. 2017 Dec 22;12(12):CD011535. doi: 10.1002/14651858.CD011535.pub2. Cochrane Database Syst Rev. 2017. Update in: Cochrane Database Syst Rev. 2020 Jan 9;1:CD011535. doi: 10.1002/14651858.CD011535.pub3. PMID: 29271481 Free PMC article. Updated.
-
Sertindole for schizophrenia.Cochrane Database Syst Rev. 2005 Jul 20;2005(3):CD001715. doi: 10.1002/14651858.CD001715.pub2. Cochrane Database Syst Rev. 2005. PMID: 16034864 Free PMC article.
Cited by
-
Why, how and in whom should we measure levels of lipoprotein(a): A review of the latest evidence and clinical implications.Diabetes Obes Metab. 2025 Sep;27 Suppl 8:34-46. doi: 10.1111/dom.16469. Epub 2025 May 28. Diabetes Obes Metab. 2025. PMID: 40437821 Free PMC article. Review.
-
Advancing Preventive Cardiology: Innovations, Care Pathways, Global Challenges, and the Future of Cardiovascular Health Across the Life Course.JACC Adv. 2025 Jun;4(6 Pt 2):101868. doi: 10.1016/j.jacadv.2025.101868. JACC Adv. 2025. PMID: 40579067 Free PMC article. No abstract available.
References
-
- Welsh P., Welsh C., Celis-Morales C.A., et al. Lipoprotein(a) and cardiovascular disease: prediction, attributable risk fraction, and estimating benefits from novel interventions. Eur J Prev Cardiol. 2021;28:1991–2000. - PubMed
-
- Clarke R., Peden J.F., Hopewell J.C., et al. Genetic variants associated with Lp(a) lipoprotein level and coronary disease. N Engl J Med. 2009;361:2518–2528. - PubMed
LinkOut - more resources
Full Text Sources
Miscellaneous