Evidence map›Paper›PMID 32293640›Full record

ArticleJAMA cardiology2020

Association Between Visit-to-Visit Blood Pressure Variability in Early Adulthood and Myocardial Structure and Function in Later Life.

Chike C Nwabuo, Yuichiro Yano, Henrique T Moreira, Duke Appiah, Henrique D Vasconcellos, Queen N Aghaji, Anthony Viera, Jamal S Rana, Ravi V Shah, Venkatesh L Murthy and 4 more

Abstract readMulticenter Study
In one paragraph

Article in JAMA cardiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Trial
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  7. Visit-to-visit blood pressure variability and clinical outcomes in peritoneal dialysis - based on machine learning algorithms.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  8. Article
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  10. Observational
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  12. Associations between long-term averages of metabolic parameters in adulthood and cardiac structure and function in later life.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Observational
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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

14 authors.

Chike C NwabuoDivision of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Yuichiro YanoDepartment of Family Medicine and Community Health, Duke University, Durham, North Carolina.
Henrique T MoreiraDivision of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Duke AppiahDepartment of Public Health, Texas Tech University Health Sciences Center, Lubbock.
Henrique D VasconcellosDivision of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Queen N AghajiDivision of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Anthony VieraDepartment of Community and Family Medicine, Duke University School of Medicine, Durham, North Carolina.
Jamal S RanaKaiser Permanente Northern California, Division of Research, Oakland.
Ravi V ShahCardiology Division, Department of Medicine, Massachusetts General Hospital, Boston.
Venkatesh L MurthyFrankel Cardiovascular Center, Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor.
Norrina B AllenNorthwestern University Feinberg School of Medicine, Chicago, Illinois.
Pamela J SchreinerUniversity of Minnesota School of Public Health, Minneapolis.
Donald M Lloyd-JonesNorthwestern University Feinberg School of Medicine, Chicago, Illinois.
João A C LimaDivision of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.

Funding

Molecular markers of early cardiometabolic health transitions in the CARDIA studyR01HL136685 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MURTHY, VENKATESH LOCHARLA, SHAH, RAVI · 2017 to 2021
$2.6M
NHLBI NIH HHS HHSN268201800003INHLBI NIH HHS HHSN268201800004INHLBI NIH HHS HHSN268201800005INHLBI NIH HHS HHSN268201800006INHLBI NIH HHS HHSN268201800007INHLBI NIH HHS R01 HL136685
6 · The paper itself

Abstract

Importance: Long-term blood pressure (BP) variability has emerged as a reproducible measure that is associated with heart failure independent of systemic BP. Visit-to-visit BP variability may be associated with the risk of heart failure early in the life course and thus may be reflected in subclinical alterations in cardiac structure and function. Objective: To evaluate the association between visit-to-visit BP variability in early adulthood and myocardial structure and function in middle age. Design, Setting, and Participants: This cohort study used data from the Coronary Artery Risk Development in Young Adults (CARDIA) study, a community-based cohort study of 5115 participants aged 18 to 30 years at baseline (year 0; March 25, 1985, to June 7, 1986) and followed up over a 30-year interval. A total of 2400 CARDIA study participants underwent evaluation at 4 field sites (Birmingham, Alabama; Oakland, California; Chicago, Illinois; and Minneapolis, Minnesota). Blood pressure was measured at 8 visits over a 25-year interval and participants received echocardiograms at year 25 (June 1, 2010, to August 31, 2011). Data analysis was conducted from June 7, 1986, to August 31, 2011. Exposures: Visit-to-visit systolic and diastolic BP variability measures included SD, average real variability, and variability independent of the mean. Main Outcomes and Measures: Echocardiographic indices of myocardial structure, systolic function, and diastolic function at the year 25 examination. Results: Of the 2400 participants, 1024 were men (42.7%) and 976 were African American (40.7%); mean (SD) age at the year 25 examination was 50.4 (3.6) years. Per 1-SD increment, greater visit-to-visit systolic BP variability independent of the mean was associated with higher left-ventricular (LV) mass index (β [SE], 2.66 [0.4] g/m2, P < .001), worse diastolic function (early peak diastolic mitral annular velocity [é]) (β [SE], -0.40 [0.1] cm/s, P < .001), higher LV filling pressures (mitral inflow velocity to early diastolic mitral annular velocity [E/é]) β [SE], 0.37 [0.1] cm/s, P < .001), and worse global longitudinal strain (β [SE], 0.17 [0.1], P = .002). Similarly, greater visit-to-visit diastolic BP variability was associated with higher LV mass index (β [SE], 3.21 [0.5] g/m2, P < .001), worse diastolic function (é: β [SE], -0.24 [0.1] cm/s [P < .001]; E/é: β [SE], 0.23 [0.1] cm/s [P < .001]), and worse global longitudinal strain (β [SE], 0.13 [0.1], P = .02). The findings remained consistent when other BP variability measures were used (SD and average real variability). Conclusions and Relevance: In this cohort study using data from the CARDIA study, greater visit-to-visit systolic and diastolic BP variability have been associated with adverse alterations in cardiac structure as well as systolic and diastolic function independent of mean BP levels.

Indexed as

AdolescentAdultBlood PressureCoronary Artery DiseaseDiastoleDisease ProgressionEchocardiographyFemaleFollow-Up StudiesHeart VentriclesHumansMaleMiddle AgedPrognosisRetrospective StudiesSystole

Identifiers

PMID32293640
PMCPMC7160747

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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.