Evidence map›Paper›PMID 39494552›Full record

ArticleJournal of the American Heart Association2024

Lipoprotein (a) Testing in Patients With Atherosclerotic Cardiovascular Disease in 5 Large US Health Systems.

Nishant P Shah, Hillary Mulder, Elizabeth Lydon, Karen Chiswell, Xingdi Hu, Zachary Lampron, Lauren Cohen, Manesh R Patel, Susan Taubes, Wenliang Song and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Nishant P ShahDivision of Cardiology Duke University Hospital Durham NC USA.ORCID 0000-0002-2666-7132
Hillary MulderDuke Clinical Research Institute Durham NC USA.ORCID 0000-0003-4838-582X
Elizabeth LydonDuke Clinical Research Institute Durham NC USA.ORCID 0009-0005-9487-8598
Karen ChiswellDuke Clinical Research Institute Durham NC USA.ORCID 0000-0002-0279-9093
Xingdi HuNovartis Pharmaceuticals Corporation East Hanover NJ USA.
Zachary LampronDuke Clinical Research Institute Durham NC USA.
Lauren CohenDuke Clinical Research Institute Durham NC USA.
Manesh R PatelDivision of Cardiology Duke University Hospital Durham NC USA.ORCID 0000-0002-2393-0855
Susan TaubesNovartis Pharmaceuticals Corporation East Hanover NJ USA.
Wenliang SongDivision of Cardiology Vanderbilt University Nashville TN USA.
Suresh R MulukutlaDivision of Cardiology University of Pittsburgh Pittsburgh PA USA.ORCID 0000-0001-5060-429X
Anum SaeedDivision of Cardiology University of Pittsburgh Pittsburgh PA USA.ORCID 0000-0003-1783-678X
Daniel P MorinDivision of Cardiology Ochsner Medical Center New Orleans LA USA.ORCID 0000-0002-9637-9507
Steven M BradleyAllina Health Minneapolis Heart Institute Minneapolis MN USA.ORCID 0000-0003-4006-6760
Adrian F HernandezDivision of Cardiology Duke University Hospital Durham NC USA.ORCID 0000-0003-3387-9616
Neha J PagidipatiDivision of Cardiology Duke University Hospital Durham NC USA.ORCID 0000-0002-5004-8868

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLipoprotein (a) is an independent risk factor for atherosclerotic cardiovascular disease. However, lipoprotein (a) testing remains variable and it is unclear what factors influence testing and if testing changes clinical management. METHODS AND

resultsA retrospective study using electronic medical record data from 5 health systems identified an atherosclerotic cardiovascular disease cohort divided into those with and without a lipoprotein (a) test between 2019 and 2021. Baseline characteristics and lipid-lowering therapy patterns were assessed. Multivariable regression modeling was used to determine factors associated with lipoprotein (a) testing. Among 595 684 patients with atherosclerotic cardiovascular disease, only 2587 (0.4%) were tested for lipoprotein (a). Those who were older or Black individuals were less likely to have lipoprotein (a) testing, while those with familial hypercholesterolemia, ischemic stroke/transient ischemic attack, peripheral artery disease, prior lipid-lowering therapy, or low-density lipoprotein cholesterol ≥130 mg/dL were more likely to be tested. Those with a lipoprotein (a) test, regardless of the lipoprotein (a) value, were more frequently initiated on any statin therapy (30.3% versus 10.6%,

conclusionsLipoprotein (a) testing in patients with atherosclerotic cardiovascular disease is infrequent, with evidence of disparities among older or Black individuals. Testing for lipoprotein (a), regardless of level, is associated with greater initiation of any lipid-lowering therapy, while elevated lipoprotein (a) is associated with greater initiation of nonstatin lipid-lowering therapy. There is a critical need for multidisciplinary and inclusive approaches to raise awareness for lipoprotein (a) testing, and its implications on management.

Indexed as

AtherosclerosisLipoprotein(a)AgedBiomarkersFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiddle AgedRetrospective StudiesRisk FactorsUnited StatesBiomarkersHydroxymethylglutaryl-CoA Reductase InhibitorsLipoprotein(a)LPA protein, humanASCVDlipidslipoprotein (a)

Identifiers

PMID39494552
PMCPMC11935684

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY-NC-ND
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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 OpenQuestion graph.