Evidence map›Paper›PMID 36645939›Full record

ArticleThe American journal of cardiology2023

Coronary Artery Calcium Dispersion and Cause-Specific Mortality.

Ramzi Dudum, Zeina A Dardari, David I Feldman, Daniel S Berman, Matthew J Budoff, Michael D Miedema, Khurram Nasir, Alan Rozanski, John A Rumberger, Leslee Shaw and 4 more

Open access · greenAbstract read
In one paragraph

Article in The American journal of cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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

14 authors at 9 institutions in 1 country.

Ramzi DudumDepartment of Cardiovascular Medicine, Stanford University, Stanford, California; Johns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, Maryland.
Zeina A DardariJohns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, Maryland.
David I FeldmanJohns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, Maryland; Department of Medicine, The Johns Hopkins Hospital, Baltimore, Maryland.
Daniel S BermanDepartment of Nuclear Cardiology/Cardiac Imaging, Cedars-Sinai Medical Center, Los Angeles, California.
Matthew J BudoffDepartment of Medicine, Harbor-UCLA Medical Center, Torrance, California.
Michael D MiedemaMinneapolis Heart Institute and Minneapolis Heart Institute Foundation, Minneapolis, Minnesota.
Khurram NasirJohns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, Maryland; Division of Cardiovascular Prevention and Wellness, Houston Methodist DeBakey Heart and Vascular Center, Houston, Texas.
Alan RozanskiDepartment of Medicine, St. Luke's Roosevelt Hospital Center, New York, New York.
John A RumbergerDepartment of Cardiovascular Imaging, Princeton Longevity Center, Princeton, New Jersey.
Leslee ShawDepartment of Radiology and Medicine, Weill Cornell Medical College, New York, New York.
Omar DzayeJohns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, Maryland.
Miguel Caínzos-AchiricaJohns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, Maryland; Division of Cardiovascular Prevention and Wellness, Houston Methodist DeBakey Heart and Vascular Center, Houston, Texas.
Jaideep PatelJohns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, Maryland; Johns Hopkins Heart and Vascular Institute at Greater Baltimore Medical Center, Baltimore, Maryland.
Michael J BlahaJohns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore, Maryland; Department of Cardiology, the Johns Hopkins Hospital, Baltimore, Maryland. Electronic address: mblaha1@jhmi.edu.
Johns Hopkins University · USHouston Methodist · USCedars-Sinai Medical Center · USCornell University · USGreater Baltimore Medical Center · USMinneapolis Heart Institute Foundation · USPrinceton University · USSt. Luke's-Roosevelt Hospital Center · USUCLA Medical Center · US

Funding

PATHOPHYSIOLOGY OF MYOCARDIAL DISEASEST32HL007227 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Chulan Kwon, WENDY S POST · 1985 to 2026
$21.2M
NHLBI NIH HHS L30 HL110027NHLBI NIH HHS T32 HL007227
6 · The paper itself

Abstract

Coronary artery calcium (CAC) measures subclinical atherosclerosis and improves risk stratification. CAC characteristics-including vessel(s) involved, number of vessels, volume, and density-have been shown to differentially impact risk. We assessed how dispersion-either the number of calcified vessels or CAC phenotype (diffuse, normal, and concentrated)-impacted cause-specific mortality. The CAC Consortium is a retrospective cohort of 66,636 participants without coronary heart disease (CHD) who underwent CAC scoring. This study included patients with CAC >0 (n = 28,147). CAC area, CAC density, and CAC phenotypes (derived from the index of diffusion = 1 - [CAC in most concentrated vessel/total Agatston score]) were calculated. The associations between CAC characteristics and cause-specific mortality were assessed. The participant details included (n = 28,147): mean age 58.3 years, 25% female, 89.6% White, and 66% had 2+ calcified vessels. Diabetes, hypertension, and hyperlipidemia were predictors of multivessel involvement (p <0.001). After controlling for the overall CAC score, those with 4-vessel CAC involvement had more CAC area and less dense calcifications than those with 1-vessel. There was a graded increase in all-cause and cardiovascular disease (CVD)- and CHD-specific mortality as the number of calcified vessels increased. Among those with ≥2 vessels involved (n = 18,516), a diffuse phenotype was associated with a higher CVD-specific mortality and had a trend toward higher all-cause and CHD-specific mortality than a concentrated CAC phenotype. Diffuse CAC involvement was characterized by less dense calcification, more CAC area, multiple coronary vessel involvement, and presence of certain traditional risk factors. There is a graded increase in all-cause and CVD- and CHD-specific mortality with increasing CAC dispersion.

Indexed as

Cardiovascular DiseasesCoronary Artery DiseaseVascular CalcificationCalciumCause of DeathCoronary AngiographyCoronary VesselsFemaleHumansMaleRetrospective StudiesRisk AssessmentRisk FactorsCalcium

Identifiers

PMID36645939
PMCPMC9928903
OpenAlexW4316170696

What OpenQuestion holds

Textmetadata
LicenceTDM
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.