Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/22946
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dc.contributor.authorPhillips, Anna Cen_UK
dc.contributor.authorRobertson, Tonyen_UK
dc.contributor.authorCarroll, Douglasen_UK
dc.contributor.authorDer, Geoffen_UK
dc.contributor.authorShiels, Paul Gen_UK
dc.contributor.authorMcGlynn, Liane Men_UK
dc.contributor.authorBenzeval, Michaelaen_UK
dc.date.accessioned2016-03-10T23:56:20Z-
dc.date.available2016-03-10T23:56:20Z-
dc.date.issued2013-04en_UK
dc.identifier.urihttp://hdl.handle.net/1893/22946-
dc.description.abstractOBJECTIVE: Psychological factors such as the stress of caregiving are emerging as predictors of telomere length, an index of biological aging. However, although lifetime major depressive disorder is associated with shorter telomeres, less is known about depressive symptoms. Depression and depressive symptoms are associated with a range of morbidities and mortality, but the extent to which they predict biological aging is unclear. The present study examined participants in the West of Scotland Twenty-07 Study across three age cohorts and four waves of data collection from 1992/1993 to 2007/2008. METHODS: Participants were 37, 57, and 76 years old at final data collection. Depressive symptoms were measured using the Hospital Anxiety and Depression Scale at each time point. Telomere length was assessed from 1063 blood samples collected at the final wave in 2007/2008 for respondents who also had depression data. RESULTS: Average depression symptoms (β= -.12, p = .047) and their change over time (β = -.12, p = .031) were negatively associated with telomere length, but only in the youngest cohort. Depressive symptoms were not cross sectionally associated with telomere length in 2007 to 2008 (β= -.03, p = .45). In the youngest cohort only, depressive symptoms assessed in 1995 to 1997 and 2000 to 2004 were associated with shorter telomere length (β = .14 [p = .046] and β = .18 [p = .012], respectively), but not 1992 to 1993 or 2007 to 2008; associations in the middle- and older-aged cohorts were nonsignificant. CONCLUSIONS: Depressive symptoms are longitudinally associated with shorter telomere length, but only in younger adults.en_UK
dc.language.isoenen_UK
dc.publisherLippincott, Williams and Wilkins for American Psychosomatic Societyen_UK
dc.relationPhillips AC, Robertson T, Carroll D, Der G, Shiels PG, McGlynn LM & Benzeval M (2013) Do symptoms of depression predict telomere length? Evidence from the west of Scotland twenty-07 study. Psychosomatic Medicine, 75 (3), pp. 288-96. https://doi.org/10.1097/PSY.0b013e318289e6b5en_UK
dc.rightsThis is a non-final version of an article published in final form in Phillips, A.C., Robertson, T., Carroll, D., Der, G., Shiels, P.G., McGlynn, L., & Benzeval, M. (2013). Do symptoms of depression predict telomere length? Evidence from the West of Scotland Twenty-07 Study. Psychosomatic Medicine, 75, 288-296. http://dx.doi.org/10.1097/PSY.0b013e318289e6b5en_UK
dc.subjectAdulten_UK
dc.subjectAgeden_UK
dc.subjectAgingen_UK
dc.subjectAging: psychologyen_UK
dc.subjectCohort Studiesen_UK
dc.subjectDepressionen_UK
dc.subjectDepression: psychologyen_UK
dc.subjectFemaleen_UK
dc.subjectFollow-Up Studiesen_UK
dc.subjectHumansen_UK
dc.subjectMaleen_UK
dc.subjectMiddle Ageden_UK
dc.subjectPsychiatric Status Rating Scalesen_UK
dc.subjectPsychiatric Status Rating Scales: statistics & numen_UK
dc.subjectRisk Factorsen_UK
dc.subjectScotlanden_UK
dc.subjectTelomereen_UK
dc.subjectTelomere Shorteningen_UK
dc.titleDo symptoms of depression predict telomere length? Evidence from the west of Scotland twenty-07 studyen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1097/PSY.0b013e318289e6b5en_UK
dc.identifier.pmid23513237en_UK
dc.citation.jtitlePsychosomatic Medicineen_UK
dc.citation.issn1534-7796en_UK
dc.citation.issn0033-3174en_UK
dc.citation.volume75en_UK
dc.citation.issue3en_UK
dc.citation.spage288en_UK
dc.citation.epage96en_UK
dc.citation.publicationstatusPublisheden_UK
dc.type.statusAM - Accepted Manuscripten_UK
dc.author.emailtony.robertson@stir.ac.uken_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationHS - Management and Support - LEGACYen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Glasgowen_UK
dc.contributor.affiliationUniversity of Glasgowen_UK
dc.contributor.affiliationMedical Research Councilen_UK
dc.identifier.isiWOS:000330467400536en_UK
dc.identifier.scopusid2-s2.0-84876285597en_UK
dc.identifier.wtid580582en_UK
dc.contributor.orcid0000-0002-5461-0598en_UK
dc.contributor.orcid0000-0002-1962-5874en_UK
dcterms.dateAccepted2013-04-30en_UK
dc.date.filedepositdate2016-03-10en_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionAMen_UK
local.rioxx.authorPhillips, Anna C|0000-0002-5461-0598en_UK
local.rioxx.authorRobertson, Tony|0000-0002-1962-5874en_UK
local.rioxx.authorCarroll, Douglas|en_UK
local.rioxx.authorDer, Geoff|en_UK
local.rioxx.authorShiels, Paul G|en_UK
local.rioxx.authorMcGlynn, Liane M|en_UK
local.rioxx.authorBenzeval, Michaela|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2016-03-10en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/all-rights-reserved|2016-03-10|en_UK
local.rioxx.filename4 PsychomaticMeddep and telomere length__proof.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source0033-3174en_UK
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