Repeated measurements of blood pressure and cholesterol improves cardiovascular disease risk prediction: an individual-participant-data meta-analysis

dc.contributor.authorPaige, Ellie
dc.contributor.authorBarrett, Jessica
dc.contributor.authorPennells, Lisa
dc.contributor.authorSweeting, Michael
dc.contributor.authorWilleit, Peter
dc.contributor.authorDi Angelantonio, Emanuele
dc.contributor.authorGudnason, Vilmundur
dc.contributor.authorNordestgaard, Borge
dc.contributor.authorPsaty, Bruce
dc.contributor.authorGoldbourt, Uri
dc.contributor.authorBest, Lyle G
dc.contributor.authorAssmann, Gerd
dc.contributor.authorSalonen, Jukka T
dc.date.accessioned2021-09-10T01:16:19Z
dc.date.available2021-09-10T01:16:19Z
dc.date.issued2017
dc.date.updated2020-11-23T11:03:21Z
dc.description.abstractThe added value of incorporating information from repeated measurements of blood pressure and cholesterol for cardiovascular disease (CVD) risk prediction has not been rigorously assessed. We used data from the Emerging Risk Factors Collaboration on 191,445 adults (38 cohorts from across 17 countries with data from 1962-2014) with > 1 million measurements of systolic blood pressure, total cholesterol and high-density lipoprotein cholesterol; over a median 12 years of follow-up, 21,170 CVD events occurred. Risk prediction models using cumulative means of repeated measurements and summary measures from longitudinal modelling of the repeated measurements were compared to models using measurements from a single time point. Risk discrimination (C-index) and net reclassification were calculated, and changes in C-indices were meta-analysed across studies. Compared to the single time point model, the cumulative means and the longitudinal models increased the C-index by 0.0040 (95% CI: 0.0023, 0.0057) and 0.0023 (0.0005, 0.0042), respectively. Reclassification was also improved in both models; compared to the single time point model, overall net reclassification improvements were 0.0369 (0.0303, 0.0436) for the cumulative means model and 0.0177 (0.0110, 0.0243) for the longitudinal model. In conclusion, incorporating repeated measurements of blood pressure and cholesterol into CVD risk prediction models slightly improves risk prediction.en_AU
dc.description.sponsorshipThis work was funded by the Medical Research Council (grants MR/L003120/1, MR/K014811/1, and G0902100), the British Heart Foundation (grant RG/13/13/30,194), and the NIHR Cambridge Biomedical Research Centre. The website of the Emerging Risk Factors Collaboration (http:// www.phpc.cam.ac.uk/ceu/erfc/list-of-studies/) contains a list, provided by investigators, of some of the funders of the component studies included in this analysis.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0002-9262en_AU
dc.identifier.urihttp://hdl.handle.net/1885/247761
dc.language.isoen_AUen_AU
dc.provenanceThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons. org/licenses/by/4.0), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.en_AU
dc.publisherOxford University Pressen_AU
dc.rights© The Author(s) 2017en_AU
dc.rights.licenseCreative Commons License (Attribution 4.0 International)en_AU
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_AU
dc.sourceAmerican Journal of Epidemiologyen_AU
dc.titleRepeated measurements of blood pressure and cholesterol improves cardiovascular disease risk prediction: an individual-participant-data meta-analysisen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.contributor.affiliationPaige, Ellie, College of Health and Medicine, ANUen_AU
local.contributor.affiliationBarrett, Jessica , University of Cambridgeen_AU
local.contributor.affiliationPennells, Lisa , University of Cambridgeen_AU
local.contributor.affiliationSweeting , Michael, University of Cambridgeen_AU
local.contributor.affiliationWilleit, Peter , University of Cambridgeen_AU
local.contributor.affiliationDi Angelantonio , Emanuele, University of Cambridgeen_AU
local.contributor.affiliationGudnason, Vilmundur, Icelandic Heart Associationen_AU
local.contributor.affiliationNordestgaard, Borge, Herlev Hospital Herlev Ringvejen_AU
local.contributor.affiliationPsaty, Bruce , University of Washingtonen_AU
local.contributor.affiliationGoldbourt , Uri, Sackler Medical School Tel Aviv Universityen_AU
local.contributor.affiliationBest , Lyle G , Missouri Breaks Industries Research Inc.en_AU
local.contributor.affiliationAssmann , Gerd , Assmann-Stiftung Fur Praventionen_AU
local.contributor.affiliationSalonen, Jukka T, University of Helsinkien_AU
local.contributor.authoruidPaige, Ellie, u4966053en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor111706 - Epidemiologyen_AU
local.identifier.absfor110201 - Cardiology (incl. Cardiovascular Diseases)en_AU
local.identifier.absfor111711 - Health Information Systems (incl. Surveillance)en_AU
local.identifier.absseo920204 - Evaluation of Health Outcomesen_AU
local.identifier.absseo920412 - Preventive Medicineen_AU
local.identifier.absseo920103 - Cardiovascular System and Diseasesen_AU
local.identifier.ariespublicationu4102339xPUB210en_AU
local.identifier.citationvolumeOnlineen_AU
local.identifier.doi10.1093/aje/kwx149en_AU
local.identifier.thomsonID000412798300001
local.type.statusPublished Versionen_AU

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