Evidence map›Paper›PMID 30575102›Full record

ArticleStatistics in medicine2019

Estimating the association between blood pressure variability and cardiovascular disease: An application using the ARIC Study.

Jessica K Barrett, Raphael Huille, Richard Parker, Yuichiro Yano, Michael Griswold

Abstract read
In one paragraph

Article in Statistics in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
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  6. Mixed-Effects Location Scale Models for Joint Modeling School Value-Added Effects on the Mean and Variance of Student Achievement.Journal of educational and behavioral statistics : a quarterly publication sponsored by the American Educational Research Association and the American Statistical Association · 2024
    Article
  7. Demographic factors associated with within-individual variability of lung function for adults with cystic fibrosis: A UK registry study.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2024
    Article
  8. Article
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  13. GWAS of longitudinal trajectories at biobank scale.American journal of human genetics · 2022
    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

5 authors.

Jessica K BarrettMRC Biostatistics Unit, University of Cambridge, Cambridge, UK.ORCID 0000-0003-1889-9803
Raphael HuilleDepartment of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
Richard ParkerSchool of Social and Community Medicine, University of Bristol, Bristol, UK.
Yuichiro YanoDepartment of Preventive Medicine, University of Mississippi Medical Center, Jackson, Mississippi.
Michael GriswoldCenter of Biostatistics and Bioinformatics, University of Mississippi Medical Center, Jackson, Mississippi.

Funding

British Heart Foundation RG/13/13/30194Medical Research Council G0800270Medical Research Council G0902100Medical Research Council MC_UU_00002/5Medical Research Council MR/K014811/1Medical Research Council MR/L003120/1Medical Research Council MR/L501566/1Medical Research Council MR/N027485/1NHLBI NIH HHS HHSN268201000021CNHLBI NIH HHS HHSN268201700001CNHLBI NIH HHS HHSN268201700001INHLBI NIH HHS HHSN268201700002CNHLBI NIH HHS HHSN268201700002INHLBI NIH HHS HHSN268201700003CNHLBI NIH HHS HHSN268201700003INHLBI NIH HHS HHSN268201700004CNHLBI NIH HHS HHSN268201700004INHLBI NIH HHS HHSN268201700005CNHLBI NIH HHS HHSN268201700005INHLBI NIH HHS HHSN268201700021C
6 · The paper itself

Abstract

The association between visit-to-visit systolic blood pressure variability and cardiovascular events has recently received a lot of attention in the cardiovascular literature. But, blood pressure variability is usually estimated on a person-by-person basis and is therefore subject to considerable measurement error. We demonstrate that hazard ratios estimated using this approach are subject to bias due to regression dilution, and we propose alternative methods to reduce this bias: a two-stage method and a joint model. For the two-stage method, in stage one, repeated measurements are modelled using a mixed effects model with a random component on the residual standard deviation (SD). The mixed effects model is used to estimate the blood pressure SD for each individual, which, in stage two, is used as a covariate in a time-to-event model. For the joint model, the mixed effects submodel and time-to-event submodel are fitted simultaneously using shared random effects. We illustrate the methods using data from the Atherosclerosis Risk in Communities study.

Indexed as

Blood PressureModels, StatisticalCardiovascular DiseasesComputer SimulationDatasets as TopicFemaleHumansLongitudinal StudiesMaleMiddle AgedPrognosisRisk FactorsSystoleUnited Statescardiovascular diseaseheteroscedasticityjoint modelmixed effects modelrepeated measurementssurvival analysis

Identifiers

PMID30575102
PMCPMC6445736

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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.