Evidence map›Paper›PMID 36621817›Full record

ArticleCirculation2023

Low-Density Lipoprotein Cholesterol Is Predominantly Associated With Atherosclerotic Cardiovascular Disease Events in Patients With Evidence of Coronary Atherosclerosis: The Western Denmark Heart Registry.

Martin Bødtker Mortensen, Omar Dzaye, Hans Erik Bøtker, Jesper Møller Jensen, Michael Maeng, Jacob Fog Bentzon, Helle Kanstrup, Henrik Toft Sørensen, Jonathon Leipsic, Ron Blankstein and 3 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Circulation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 4 pooled it
42.5field-weighted citation impact, top 1% of its field
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

76 citing papers in PubMed, 4 syntheses or guidelines pooled it, 134 citations in OpenAlex.

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16 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 4 countries.

Martin Bødtker Mortensen *Departments of Cardiology (M.B.M., H.E.B., J.M.J., M.M., J.F.B., H.K., B.L.N.), Aarhus University Hospital, Denmark.ORCID 0000-0003-2693-4154
Omar Dzaye *Johns Hopkins Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, MD (M.B.M., O.D., M.J.B.).ORCID 0000-0001-9483-3510
Hans Erik BøtkerDepartments of Cardiology (M.B.M., H.E.B., J.M.J., M.M., J.F.B., H.K., B.L.N.), Aarhus University Hospital, Denmark.ORCID 0000-0001-6358-8962
Jesper Møller JensenDepartments of Cardiology (M.B.M., H.E.B., J.M.J., M.M., J.F.B., H.K., B.L.N.), Aarhus University Hospital, Denmark.
Michael MaengDepartments of Cardiology (M.B.M., H.E.B., J.M.J., M.M., J.F.B., H.K., B.L.N.), Aarhus University Hospital, Denmark.ORCID 0000-0002-4310-6433
Jacob Fog BentzonDepartments of Cardiology (M.B.M., H.E.B., J.M.J., M.M., J.F.B., H.K., B.L.N.), Aarhus University Hospital, Denmark.ORCID 0000-0002-3020-5002
Helle KanstrupDepartments of Cardiology (M.B.M., H.E.B., J.M.J., M.M., J.F.B., H.K., B.L.N.), Aarhus University Hospital, Denmark.
Henrik Toft SørensenClinical Epidemiology (H.T.S.), Aarhus University Hospital, Denmark.ORCID 0000-0003-4299-7040
Jonathon LeipsicSt Pauls Hospital, UBC, VancouverCanada (J.L.).
Ron BlanksteinCardiovascular Division and Department of Radiology, Brigham and Women's Hospital, Boston, MA (R.B.).
Khurram NasirDivision of Cardiovascular Prevention and Wellness, Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, TX (K.N.).ORCID 0000-0001-5376-2269
Michael J BlahaJohns Hopkins Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, MD (M.B.M., O.D., M.J.B.).ORCID 0000-0001-5138-9683
Bjarne Linde NørgaardDepartments of Cardiology (M.B.M., H.E.B., J.M.J., M.M., J.F.B., H.K., B.L.N.), Aarhus University Hospital, Denmark.
Aarhus University Hospital · DKJohns Hopkins University · USBrigham and Women's Hospital · USHouston Methodist · USSt. Paul's Hospital · CA

Funding

Institute for Clinical and Translational ResearchUL1TR001079 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2013 to 2017
$60.1M
Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3M
Clinical and Translational Science AwardUL1TR000040 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GINSBERG, HENRY N · 2012 to 2015
$26.2M
PATHOPHYSIOLOGY OF MYOCARDIAL DISEASEST32HL007227 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Chulan Kwon, WENDY S POST · 1985 to 2026
$21.2M
NCATS NIH HHS UL1 TR000040NCATS NIH HHS UL1 TR001079NCATS NIH HHS UL1 TR001420NHLBI NIH HHS T32 HL007227
6 · The paper itself

Abstract

backgroundLow-density lipoprotein cholesterol (LDL-C) is an important causal risk factor for atherosclerotic cardiovascular disease (ASCVD). However, a sizable proportion of middle-aged individuals with elevated LDL-C level have not developed coronary atherosclerosis as assessed by coronary artery calcification (CAC). Whether presence of CAC modifies the association of LDL-C with ASCVD risk is unknown. We evaluated the association of LDL-C with future ASCVD events in patients with and without CAC.

methodsThe study included 23 132 consecutive symptomatic patients evaluated for coronary artery disease using coronary computed tomography angiography (CTA) from the Western Denmark Heart Registry, a seminational, multicenter-based registry with longitudinal registration of patient and procedure data. We assessed the association of LDL-C level obtained before CTA with ASCVD (myocardial infarction and ischemic stroke) events occurring during follow-up stratified by CAC>0 versus CAC=0 using Cox regression models adjusted for baseline characteristics. Outcomes were identified through linkage among national registries covering all hospitals in Denmark. We replicated our results in the

resultsDuring a median follow-up of 4.3 years, 552 patients experienced a first ASCVD event. In the overall population, LDL-C (per 38.7 mg/dL increase) was associated with ASCVD events occurring during follow-up (adjusted hazard ratio [aHR], 1.14 [95% CI, 1.04-1.24]). When stratified by the presence or absence of baseline CAC, LDL-C was only associated with ASCVD in the 10 792/23 132 patients (47%) with CAC>0 (aHR, 1.18 [95% CI, 1.06-1.31]); no association was observed among the 12 340/23 132 patients (53%) with CAC=0 (aHR, 1.02 [95% CI, 0.87-1.18]). Similarly, a very high LDL-C level (

conclusionsLDL-C appears to be almost exclusively associated with ASCVD events over ≈5 years of follow-up in middle-aged individuals with versus without evidence of coronary atherosclerosis. This information is valuable for individualized risk assessment among middle-aged people with or without coronary atherosclerosis.

Indexed as

AtherosclerosisCardiovascular DiseasesCoronary Artery DiseaseVascular CalcificationCholesterol, LDLDenmarkHumansMiddle AgedRegistriesRisk AssessmentRisk FactorsCholesterol, LDLarteriescalciumcardiovascular diseasescohort studiescomputed tomography angiographycoronary artery diseasecoronary vesselsepidemiologylipoproteins, LDLrisk

Identifiers

PMID36621817
PMCPMC10073288
OpenAlexW4313827809

What OpenQuestion holds

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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.