Evidence map›Paper›PMID 30961992›Full record

ArticleAnnals of epidemiology2019

Racial and sex differences in biological and chronological heart age in the Coronary Artery Risk Development in Young Adults study.

Rachel Zmora, Pamela J Schreiner, Duke Appiah, Donald M Lloyd-Jones, Jamal S Rana, Cora E Lewis

Open access · greenAbstract read
In one paragraph

Article in Annals of epidemiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  3. Child Marriage and Cardiovascular Risk: An Application of the Non-laboratory Framingham Risk Score.High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension · 2024
    Article
  4. 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

6 authors at 5 institutions in 1 country.

Rachel ZmoraDivision of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis. Electronic address: zmora005@umn.edu.
Pamela J SchreinerDivision of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis.
Duke AppiahGraduate School of Biomedical Sciences, Texas Tech University Health Sciences Center, Lubbock.
Donald M Lloyd-JonesFeinberg School of Medicine, Northwestern University, Chicago, IL.
Jamal S RanaDivision of Research, Department of Cardiology, Kaiser Permanente Northern California, Oakland.
Cora E LewisDepartment of Medicine, University of Alabama at Birmingham, Birmingham.
University of Minnesota · USKaiser Permanente · USNorthwestern University · USTexas Tech University · USUniversity of Alabama at Birmingham · US

Funding

NHLBI NIH HHS HHSN268200900041CNHLBI NIH HHS HHSN268201000031CNHLBI NIH HHS HHSN268201000041CNHLBI NIH HHS HHSN268201000051CNHLBI NIH HHS HHSN268201100007INHLBI NIH HHS HHSN268201300025CNHLBI NIH HHS HHSN268201300026CNHLBI NIH HHS HHSN268201300027CNHLBI NIH HHS HHSN268201300028CNHLBI NIH HHS HHSN268201300029CNHLBI NIH HHS HHSN268201800006I
6 · The paper itself

Abstract

purposeCalculation of a biological heart age offers an alternative to absolute risk for characterizing cardiovascular risk by describing risk relative to an individual with normal health. We examined risk factors contributing to differences between biological and chronological heart age in young adults.

methodsThe Coronary Artery Risk Development in Young Adults study included 2264 Black and White men and women who attended examination years 10 through 25. We estimated biological heart age using the nonlaboratory-based Framingham 10-year cardiovascular disease risk calculator. Trends in risk factors were examined cross-sectionally and longitudinally.

resultsBiological heart ages for Black participants were 5.6 years older than their chronological ages over 15 years (P < .001). In longitudinal analyses, urinary albumin-creatinine ratio and alcohol intake were statistically significantly related to higher biological compared with chronological heart age, whereas physical activity and education were statistically significantly related to negative heart age differences (P < .001). Trends were similar in cross-sectional analyses at all time points.

conclusionsMost risk factors driving biological heart age, including race, education, physical activity, and urinary albumin-creatinine ratio, contributed to heart age differences cross-sectionally and longitudinally suggesting that risk factors related to adverse biological aging are important at younger and older ages.

Indexed as

Age FactorsAgingHealth Status DisparitiesAdultAgedBlack or African AmericanBlack PeopleCardiovascular DiseasesCross-Sectional StudiesFemaleHumansLongitudinal StudiesMaleRisk FactorsSex FactorsSocioeconomic FactorsAgingCardiovascular diseasesPrevention and control

Identifiers

PMID30961992
PMCPMC6743489
OpenAlexW2919683812

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.