Evidence map›Paper›PMID 33212181›Full record

ArticleJournal of the American Society of Echocardiography : official publication of the American Society of Echocardiography2021

Age-Related Development of Cardiac Remodeling and Dysfunction in Young Black and White Adults: The Coronary Artery Risk Development in Young Adults Study.

Amanda M Perak, Sadiya S Khan, Laura A Colangelo, Samuel S Gidding, Anderson C Armstrong, Cora E Lewis, Jared P Reis, Pamela J Schreiner, Stephen Sidney, Joao A C Lima and 1 more

Abstract read
In one paragraph

Article in Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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  6. Article
  7. Article
  8. Review
  9. Review
  10. Bending Primordial Trajectories Away From Heart Failure.Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography · 2021
    Article
  11. Article
  12. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Amanda M PerakNorthwestern University, Chicago, Illinois; Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois. Electronic address: amarma@luriechildrens.org.
Sadiya S KhanNorthwestern University, Chicago, Illinois.
Laura A ColangeloNorthwestern University, Chicago, Illinois.
Samuel S GiddingThe Familial Hypercholesterolemia Foundation, Pasadena, California.
Anderson C ArmstrongJohns Hopkins University, Baltimore, Maryland; University of Sao Francisco Valley, Petrolina, Brazil.
Cora E LewisUniversity of Alabama at Birmingham, Birmingham, Alabama.
Jared P ReisNational Heart, Lung, and Blood Institute, Bethesda, Maryland.
Pamela J SchreinerUniversity of Minnesota, Minneapolis, Minnesota.
Stephen SidneyKaiser Permanente, Oakland, California.
Joao A C LimaJohns Hopkins University, Baltimore, Maryland.
Donald M Lloyd-JonesNorthwestern University, Chicago, Illinois.

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
Northwestern University Clinical and Translational Science Institute (NUCATS)KL2TR001424 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SHARMA, LEENA · 2015 to 2023
$8.1M
RESEARCH TRAINING IN CVD EPIDEMIOLOGY AND PREVENTIONT32HL069771 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Mercedes Renee Carnethon · 2003 to 2026
$5.9M
Response of the Gut Microbiome and Circulating Metabolome to Diet Intervention in Young Children: Ancillary Study to the Keeping Ideal Cardiovascular Health Family Intervention Trial (KIDFIT)K23HL145101 · NHLBI · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI MARMA, AMANDA K · 2019 to 2023
$948k
NCATS NIH HHS KL2 TR001424NCATS NIH HHS UL1 TR001422NHLBI NIH HHS HHSN268200900041CNHLBI NIH HHS HHSN268201800003INHLBI NIH HHS HHSN268201800004INHLBI NIH HHS HHSN268201800005INHLBI NIH HHS HHSN268201800006INHLBI NIH HHS HHSN268201800007INHLBI NIH HHS K23 HL145101NHLBI NIH HHS T32 HL069771
6 · The paper itself

Abstract

backgroundLittle is known about the timing of preclinical heart failure (HF) development, particularly among blacks. The primary aims of this study were to delineate age-related left ventricular (LV) structure and function evolution in a biracial cohort and to test the hypothesis that young-adult LV parameters within normative ranges would be associated with incident stage B-defining LV abnormalities over 25 years, independent of cumulative risk factor burden.

methodsData from the Coronary Artery Risk Development in Young Adults study were analyzed. Participants (n = 2,833) had a mean baseline age of 30.1 years; 45% were black, and 56% were women. Generalized estimating equation logistic regression was used to estimate age-related probabilities of stage B LV abnormalities (remodeling, hypertrophy, or dysfunction) and logistic regression to examine risk factor-adjusted associations between baseline LV parameters and incident abnormalities. Cox regression was used to assess whether baseline LV parameters associated with incident stage B LV abnormalities were also associated with incident clinical (stage C/D) HF events over >25 years' follow-up.

resultsProbabilities of stage B LV abnormalities at ages 25 and 60 years were 10.5% (95% CI, 9.4%-11.8%) and 45.0% (95% CI, 42.0%-48.1%), with significant race-sex disparities (e.g., at age 60, black men 52.7% [95% CI, 44.9%-60.3%], black women 59.4% [95% CI, 53.6%-65.0%], white men 39.1% [95% CI, 33.4%-45.0%], and white women 39.1% [95% CI, 33.9%-44.6%]). Over 25 years, baseline LV end-systolic dimension indexed to height was associated with incident systolic dysfunction (adjusted odds ratio per 1 SD higher, 2.56; 95% CI, 1.87-3.52), eccentric hypertrophy (1.34; 95% CI, 1.02-1.75), concentric hypertrophy (0.69; 95% CI, 0.51-0.91), and concentric remodeling (0.68; 95% CI, 0.58-0.79); baseline LV mass indexed to height

conclusionsStage B LV abnormalities and related racial disparities were present in young adulthood, increased with age, and were associated with baseline variation in indexed LV end-systolic dimension and mass. Baseline indexed LV end-systolic dimension and mass were also associated with incident clinical HF. Efforts to prevent the LV abnormalities underlying clinical HF should start from a young age.

Indexed as

Heart FailureVentricular RemodelingAdultBlack or African AmericanCoronary VesselsFemaleHeart VentriclesHumansHypertrophy, Left VentricularInfant, NewbornMaleMiddle AgedRisk FactorsYoung AdultDisparitiesHeart failureLeft ventricle

Identifiers

PMID33212181
PMCPMC8026546

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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.