Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/22239
Full metadata record
DC FieldValueLanguage
dc.contributor.authorEvans, Josieen_UK
dc.contributor.authorEades, Claireen_UK
dc.contributor.authorLeese, Grahamen_UK
dc.date.accessioned2015-10-06T23:43:37Z-
dc.date.available2015-10-06T23:43:37Z-
dc.date.issued2015-09-16en_UK
dc.identifier.othere000102en_UK
dc.identifier.urihttp://hdl.handle.net/1893/22239-
dc.description.abstractObjective: Mortality among adults of all ages diagnosed with impaired glucose regulation (IGR) in Tayside, Scotland, UK, was evaluated using routinely collected healthcare data sets.  Research design and methods: Using record-linked data in 2003–2008, all instances of blood glucose testing in the population defined 2 cohorts of patients aged 18+years: those with IGR (whether impaired fasting glucose or impaired glucose tolerance (IGT)) according to the WHO criteria, and those who were normoglycemic. They were followed in survival analyses for mortality or cardiovascular mortality (censoring deaths that occurred within a 30-day period of testing), to derive HRs (with 95% CI) for IGR status using Cox regression, adjusted for age, sex, and an area measure of deprivation.  Results: There were 2 372 712 tests for 214 094 patients, with 196 799 patients in the non-IGR cohort and 50 080 in the IGR cohort. During follow-up, 19 147 (9.7%) and 8397 (16.8%) patients died in 2 cohorts, respectively, with mortality rates of 33.2/1000 patient-years and 70.7/1000 patient-years. In multivariable analyses, the overall adjusted risk of mortality for IGR was 1.16 (95% CI 1.13 to 1.20). However, it was 2.59 (95% CI 2.17 to 3.10) for people aged <45 years, decreasing to 0.94 (95% CI 0.85 to 1.00) in those aged 85+years. The HRs for cardiovascular mortality were lower overall, but they followed the same pattern, with statistically significant increased risks for patients aged <64 years only. The mortality risk was highest among patients with IGT.  Conclusions: IGR is associated with an increased mortality risk which declines with age. It is therefore important to prioritize young people with IGR for prevention; but less important to be aggressive about risk factor modification in older people.en_UK
dc.language.isoenen_UK
dc.publisherBMJ Publishing Groupen_UK
dc.relationEvans J, Eades C & Leese G (2015) The risk of total mortality and cardiovascular mortality associated with impaired glucose regulation in Tayside, Scotland, UK: a record-linkage study in 214 094 people. BMJ Open Diabetes Research and Care, 3 (1), Art. No.: e000102. http://drc.bmj.com/content/3/1/e000102?cpetoc; https://doi.org/10.1136/bmjdrc-2015-000102en_UK
dc.rightsThis is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/en_UK
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/en_UK
dc.titleThe risk of total mortality and cardiovascular mortality associated with impaired glucose regulation in Tayside, Scotland, UK: a record-linkage study in 214 094 peopleen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1136/bmjdrc-2015-000102en_UK
dc.identifier.pmid26405556en_UK
dc.citation.jtitleBMJ Open Diabetes Research and Careen_UK
dc.citation.issn2052-4897en_UK
dc.citation.volume3en_UK
dc.citation.issue1en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.identifier.urlhttp://drc.bmj.com/content/3/1/e000102?cpetocen_UK
dc.author.emailjosie.evans@stir.ac.uken_UK
dc.citation.date16/09/2015en_UK
dc.contributor.affiliationHealth Sciences Research - Stirling - LEGACYen_UK
dc.contributor.affiliationHealth Sciences Research - Stirling - LEGACYen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.identifier.wtid589322en_UK
dc.contributor.orcid0000-0001-6672-7876en_UK
dc.contributor.orcid0000-0002-4845-332Xen_UK
dc.date.accepted2015-06-09en_UK
dcterms.dateAccepted2015-06-09en_UK
dc.date.filedepositdate2015-09-17en_UK
rioxxterms.apcpaiden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorEvans, Josie|0000-0001-6672-7876en_UK
local.rioxx.authorEades, Claire|0000-0002-4845-332Xen_UK
local.rioxx.authorLeese, Graham|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2015-09-17en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by-nc/4.0/|2015-09-17|en_UK
local.rioxx.filenameEvans et al_BMJ Open Diabetes Research and Care_2015.pdfen_UK
local.rioxx.filecount1en_UK
Appears in Collections:Faculty of Health Sciences and Sport Journal Articles

Files in This Item:
File Description SizeFormat 
Evans et al_BMJ Open Diabetes Research and Care_2015.pdfFulltext - Published Version424.63 kBAdobe PDFView/Open


This item is protected by original copyright



A file in this item is licensed under a Creative Commons License Creative Commons

Items in the Repository are protected by copyright, with all rights reserved, unless otherwise indicated.

The metadata of the records in the Repository are available under the CC0 public domain dedication: No Rights Reserved https://creativecommons.org/publicdomain/zero/1.0/

If you believe that any material held in STORRE infringes copyright, please contact library@stir.ac.uk providing details and we will remove the Work from public display in STORRE and investigate your claim.