Evidence map›Paper›PMID 41338528›Full record

ArticleJournal of stroke and cerebrovascular diseases : the official journal of National Stroke Association2026

Lipoprotein(a) testing trends in young ischemic stroke patients from 2015-2024: An analysis of 188,000 individuals.

Mustafa Naguib, Brett C Meyer, Francesca Felipe, Raphael E Cuomo, Michael Wilkinson, Ehtisham Mahmud, Pam Taub, Harpreet S Bhatia, Mattheus Ramsis

Abstract read
In one paragraph

Article in Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Mustafa NaguibDivision of Cardiovascular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA, USA. Electronic address: mhnaguib@health.ucsd.edu.
Brett C MeyerDivision of Vascular Neurology, Department of Neurosciences, University of California San Diego, La Jolla, CA, USA. Electronic address: bcmeyer@health.ucsd.edu.
Francesca FelipeDivision of Cardiovascular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA, USA. Electronic address: ffelipe@ucsd.edu.
Raphael E CuomoDepartment of Anesthesiology, School of Medicine, University of California San Diego, La Jolla, CA, USA. Electronic address: rcuomo@health.ucsd.edu.
Michael WilkinsonDivision of Cardiovascular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA, USA. Electronic address: mjwilkinson@health.ucsd.edu.
Ehtisham MahmudDivision of Cardiovascular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA, USA. Electronic address: emahmud@health.ucsd.edu.
Pam TaubDivision of Cardiovascular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA, USA. Electronic address: ptaub@health.ucsd.edu.
Harpreet S BhatiaDivision of Cardiovascular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA, USA. Electronic address: hsbhatia@health.ucsd.edu.
Mattheus RamsisDivision of Cardiovascular Medicine, Department of Medicine, University of California San Diego, La Jolla, CA, USA. Electronic address: mramsis@ucsd.edu.

Funding

Aspirin for Primary Prevention of Cardiovascular Disease in Patients with Elevated Lipoprotein(a)K08HL166962 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Harpreet Singh Bhatia · 2023 to 2026
$676k
NHLBI NIH HHS K08 HL166962
6 · The paper itself

Abstract

backgroundLipoprotein(a) [Lp(a)] is a genetically determined risk factor for myocardial infarction and stroke. Elevated Lp(a) >50 mg/dL (>125 nmol/L) is common and present in about 1 in 5 individuals. Although Lp(a) may be a cause of young ischemic stroke (age ≤60), limited data on national testing trends in this population are available, testing in the general population remains low overall, and different organizations have varying guidelines for testing. By determining the degree to which this population is tested, information on national testing trends of Lp(a) in young ischemic stroke patients may influence future guideline recommendations to increase Lp(a) testing. This study aims to use a large, real-world dataset to assess trends of Lp(a) testing in young ischemic stroke patients in the United States from 2015-2024.

methodsWe performed a retrospective analysis of Lp(a) testing in young ischemic stroke patients across the United States from January 1, 2015 to December 31, 2024 using Epic Cosmos, a nationwide, de-identified electronic health record (EHR) dataset comprising over 300 million patient records from over 1,715 hospitals and 41,000 clinics, including from all 50 states, Washington D.C., Lebanon, and Saudi Arabia. The current count values for patients, hospitals, and clinics are available on the Epic Cosmos website. Although the Epic Cosmos data dictionary includes Lebanon and Saudi Arabia as standardized site locations, no patients from these countries were present in our analytic cohort; thus, all analyses were restricted to individuals within the United States. We evaluated the number of young ischemic stroke patients, defined as age ≤60 with history of an ischemic cerebrovascular accident (CVA), who had ever undergone Lp(a) testing, the testing rate per annual young ischemic stroke patients, geographical variation, and percentages of patients tested stratified by age, sex, ethnicity, race, and diagnosis of coronary artery disease (CAD). Testing rates were calculated as the number of distinct patients tested per year and as the testing rate per annual patient population. For each stratum we calculated the proportion tested with Wilson 95 % confidence intervals and assessed between-group differences using chi square or Fisher exact tests as appropriate. Annual trends in the testing proportion were modeled using a binomial generalized linear model with a logit link, treating the annual number tested as the numerator and the annual young ischemic stroke population as the denominator, and we report the odds ratio per calendar year with robust standard errors. Geographical variation was visualized using a heat map of testing by state. All analyses were descriptive and intended to characterize population-level patterns of ischemic stroke within the Cosmos network rather than infer causal associations. Given the exploratory design, no additional model-based adjustment for confounding was performed. All data are de-identified in compliance with HIPAA standards and governed under Epic's "Rules of the Road" for institutional data use.

resultsFrom 2015 to 2024, out of a total of 188,305 distinct young ischemic stroke patients, 9,226 (4.9 %) underwent Lp(a) testing. Additionally, the annual number of tested patients increased significantly from 179 in 2015 to 1,992 in 2024 (p<0.001), and the annual percentage of patients undergoing Lp(a) testing increased from 4.3 % in 2015 to 9.3 % in 2024. The states with the largest number of tested patients were Ohio (10.4 %), Texas (7.4 %), and Pennsylvania (5.5 %). The rates of testing were significantly different between sexes, with a larger percentage of young women with ischemic strokes tested compared to young men. Analyzing patients with reported racial data, patients who identified as Black or African American underwent testing for Lp(a) at the highest rate, compared with patients who identified as Asian, "None of the above", White, or Other Race. Among patients undergoing testing with reported ethnic identity, a higher percentage of patients who identified as Hispanic or Latino were tested compared to those who identified as non-Hispanic. Stratifying the total tested patients by age, adults between the ages of 50-60 years made up the largest percentage of patients (4,460; 48.3 %); however, the highest rate of testing occurred in patients aged 5-18. In addition, a higher rate of the young ischemic stroke patients who had ever had a diagnosis of CAD underwent testing compared to patients without CAD. DISCUSSION: Lp(a) testing among young ischemic stroke patients has increased significantly over the past decade, likely reflecting growing clinical recognition of its causal role in atherosclerotic disease. The rise parallels key updates in lipid management and stroke prevention guidelines, including the 2019 European Society of Cardiology and 2024 National Lipid Association recommendations advocating at least once-in-a-lifetime Lp(a) measurement. Increasing assay availability and heightened awareness of the causal relationship of Lp(a) with atherosclerotic disease may also have contributed to the observed upward trend. Despite this, only about one in twenty young ischemic stroke patients had ever been tested, underscoring a substantial implementation gap between evidence and clinical practice.

Indexed as

Brain IschemiaIschemic StrokeLipoprotein(a)Practice Patterns, Physicians'StrokeAdolescentAdultAge FactorsBiomarkersDatabases, FactualFemaleHumansMaleMiddle AgedPredictive Value of TestsRetrospective StudiesBiomarkersLipoprotein(a)LPA protein, humanAtherosclerosisBioinformaticsElectronic health recordEpidemiologyIschemic stroke in young adultsLarge datasetLipoprotein(a)Stroke prevention

Identifiers

PMID41338528
PMCPMC13361849

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.