Evidence map›Paper›PMID 28888270›Full record

ArticleAmerican heart journal2017

Soluble endothelial cell-selective adhesion molecule and incident cardiovascular events in a multiethnic population.

Hao-Yu Ren, Amit Khera, James A de Lemos, Colby R Ayers, Anand Rohatgi

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in American heart journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 37% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Hao-Yu RenDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX.
Amit KheraDivision of Cardiology, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX.
James A de LemosDivision of Cardiology, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX.
Colby R AyersDivision of Cardiology, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX.
Anand RohatgiDivision of Cardiology, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX. Electronic address: Anand.rohatgi@utsouthwestern.edu.
Southwestern Medical Center · US

Funding

UT Southwestern Center for Translational Medicine (UL1/KL2/TL1)UL1TR001105 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2013 to 2017
$24.5M
Moving Beyond HDL Cholesterol, HDL Function as a Coronary Disease BiomarkerK08HL118131 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI ROHATGI, ANAND KUMAR · 2013 to 2017
$665k
NCATS NIH HHS UL1 TR001105NHLBI NIH HHS K08 HL118131
6 · The paper itself

Abstract

backgroundCell adhesion molecules are key regulators of atherosclerotic plaque development, but circulating levels of soluble fragments, such as intercellular adhesion molecule (sICAM-1) and vascular cell adhesion molecule (sVCAM-1), have yielded conflicting associations with atherosclerotic cardiovascular disease (ASCVD). Endothelial cell-selective adhesion molecule (ESAM) is expressed exclusively in platelets and endothelial cells, and soluble ESAM (sESAM) levels have been associated with prevalent subclinical atherosclerosis. We therefore hypothesized that sESAM would be associated with incident ASCVD.

methodssESAM, sICAM-1, and sVCAM-1 were measured in 2,442 participants without CVD in the Dallas Heart Study, a probability-based population sample aged 30-65 years enrolled between 2000 and 2002. ASCVD was defined as first myocardial infarction, stroke, coronary revascularization, or CV death. A total of 162 ASCVD events were analyzed over 10.4 years.

resultsIncreasing sESAM was associated with ASCVD, independent of risk factors (HR Q4 vs Q1: 2.7, 95% CI 1.6-4.6). Serial adjustment for renal function, sICAM-1, VCAM-1, and prevalent coronary calcium did not attenuate these associations. Continuous ESAM demonstrated similar findings (HR 1.31, 95% CI 1.2-1.4). Addition of sESAM to traditional risk factors improved discrimination and reclassification (delta c-index: P = .009; integrated-discrimination-improvement index P = .001; net reclassification index = 0.42, 95% CI 0.15-0.68). Neither sICAM-1 nor sVCAM-1 was independently associated with ASCVD.

conclusionssESAM but not sICAM-1 or sVCAM-1 levels are associated with incident ASCVD. Further studies are warranted to investigate the role of sESAM in ASCVD.

Indexed as

EthnicityPopulation SurveillanceRisk AssessmentAdultAgedBiomarkersCardiovascular DiseasesCell Adhesion MoleculesFemaleHumansIncidenceIntercellular Adhesion Molecule-1MaleMiddle AgedPrognosisTexasBiomarkersCell Adhesion MoleculesESAM protein, humanIntercellular Adhesion Molecule-1Vascular Cell Adhesion Molecule-1

Identifiers

PMID28888270
PMCPMC5657571
OpenAlexW2638831393

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

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.