Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/32787
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dc.contributor.authorThomas, G Neilen_UK
dc.contributor.authorPhillips, Anna C.en_UK
dc.contributor.authorCarroll, Douglasen_UK
dc.contributor.authorGale, Catharine Ren_UK
dc.contributor.authorBatty, G Daviden_UK
dc.date.accessioned2021-06-26T00:02:33Z-
dc.date.available2021-06-26T00:02:33Z-
dc.date.issued2010-05en_UK
dc.identifier.urihttp://hdl.handle.net/1893/32787-
dc.description.abstractBackground The metabolic syndrome increases mortality risk. However, as “non-affected” individuals may still have up to two risk factors, the utility of using three or more components to identify the syndrome, and its predictive advantage over individual components have yet to be determined. Methods Participants, male Vietnam-era veterans (n = 4265) from the USA, were followed-up from 1985/1986 for 14.7 years (61,498 person-years), and all-cause and cardiovascular disease deaths collated. Cox's proportional-hazards regression was used to assess the effect of the metabolic syndrome and its components on mortality adjusting for a wide range of potential confounders. Results At baseline, 752 participants (17.9%) were identified as having metabolic syndrome. There were 231 (5.5%) deaths from all-causes, with 60 from cardiovascular disease. After adjustment for a range of covariates, the metabolic syndrome increased the risk of all-cause, HR 2.03, 95%CI 1.52, 2.71, and cardiovascular disease mortality, HR 1.92, 95%CI 1.10, 3.36. Risk increased dose-dependently with increasing numbers of components. The increased risk from possessing only one or two components was not statistically significant. The adjusted risk for four or more components was greater than for only three components for both all-cause, HR 2.30, 95%CI 1.45, 3.66 vs. HR 1.70, 95%CI 1.11, 2.61, and cardiovascular disease mortality, HR 3.34, 95%CI 1.19, 9.37 vs. HR 2.81, 95%CI 1.07, 7.35. The syndrome was more informative than the individual components for all-cause mortality, but could not be assessed for cardiovascular disease mortality due to multicollinearity. Hyperglycaemia was the individual strongest parameter associated with mortality. Conclusions The metabolic syndrome is informative in predicting mortality, with risk increasing as the number of components increase above the threshold required for diagnosis.en_UK
dc.language.isoenen_UK
dc.publisherElsevier BVen_UK
dc.relationThomas GN, Phillips AC, Carroll D, Gale CR & Batty GD (2010) The metabolic syndrome adds utility to the prediction of mortality over its components: The Vietnam Experience Study. Atherosclerosis, 210 (1), pp. 256-261. https://doi.org/10.1016/j.atherosclerosis.2009.10.045en_UK
dc.rightsThe publisher does not allow this work to be made publicly available in this Repository. Please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study.en_UK
dc.rights.urihttp://www.rioxx.net/licenses/under-embargo-all-rights-reserveden_UK
dc.subjectAll-causeen_UK
dc.subjectCardiovascular diseaseen_UK
dc.subjectMetabolic syndromeen_UK
dc.subjectMortalityen_UK
dc.subjectVeteransen_UK
dc.titleThe metabolic syndrome adds utility to the prediction of mortality over its components: The Vietnam Experience Studyen_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate2999-12-31en_UK
dc.rights.embargoreason[ATH11191.pdf] The publisher does not allow this work to be made publicly available in this Repository therefore there is an embargo on the full text of the work.en_UK
dc.identifier.doi10.1016/j.atherosclerosis.2009.10.045en_UK
dc.identifier.pmid20004895en_UK
dc.citation.jtitleAtherosclerosisen_UK
dc.citation.issn0021-9150en_UK
dc.citation.volume210en_UK
dc.citation.issue1en_UK
dc.citation.spage256en_UK
dc.citation.epage261en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderNational Center for Environmental Health, Atlanta, USen_UK
dc.author.emaila.c.whittaker@stir.ac.uken_UK
dc.citation.date10/11/2009en_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.identifier.isiWOS:000277085300042en_UK
dc.identifier.scopusid2-s2.0-77952425400en_UK
dc.identifier.wtid1476332en_UK
dc.contributor.orcid0000-0002-5461-0598en_UK
dc.date.accepted2009-10-28en_UK
dcterms.dateAccepted2009-10-28en_UK
dc.date.filedepositdate2019-11-05en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorThomas, G Neil|en_UK
local.rioxx.authorPhillips, Anna C.|0000-0002-5461-0598en_UK
local.rioxx.authorCarroll, Douglas|en_UK
local.rioxx.authorGale, Catharine R|en_UK
local.rioxx.authorBatty, G David|en_UK
local.rioxx.projectProject ID unknown|National Center for Environmental Health, Atlanta, US|en_UK
local.rioxx.freetoreaddate2259-10-11en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved||en_UK
local.rioxx.filenameATH11191.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source0021-9150en_UK
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