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dc.contributor.authorPilling, LC
dc.contributor.authorJones, LC
dc.contributor.authorMasoli, JAH
dc.contributor.authorDelgado, J
dc.contributor.authorAtkins, JL
dc.contributor.authorBowden, J
dc.contributor.authorFortinsky, RH
dc.contributor.authorKuchel, GA
dc.contributor.authorMelzer, D
dc.date.accessioned2020-10-06T12:46:52Z
dc.date.issued2020-10-05
dc.description.abstractBACKGROUND/OBJECTIVES Delirium is common in older adults, especially following hospitalization. Because low vitamin D levels may be associated with increased delirium risk, we aimed to determine the prognostic value of blood vitamin D levels, extending our previous genetic analyses of this relationship. DESIGN Prospective cohort analysis. SETTING Community‐based cohort study of adults from 22 cities across the United Kingdom (the UK Biobank). PARTICIPANTS Adults aged 60 and older by the end of follow‐up in the linked hospital inpatient admissions data, up to 14 years after baseline (n = 351,320). MEASUREMENTS At baseline, serum vitamin D (25‐OH‐D) levels were measured. We used time‐to‐event models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for the association between vitamin D deficiency and incident hospital‐diagnosed delirium, adjusted for age, sex, assessment month, assessment center, and ethnicity. We performed Mendelian randomization genetic analysis in European participants to further investigate vitamin D and delirium risk. RESULTS A total of 3,634 (1.03%) participants had at least one incident hospital‐diagnosed delirium episode. Vitamin D deficiency (<25 nmol/L) predicted a large incidence in delirium (HR = 2.49; 95% CI = 2.24–2.76; P = 3*10−68, compared with >50 nmol/L). Increased risk was not limited to the deficient group: insufficient levels (25–50 nmol/L) were also at increased risk (HR = 1.38; 95% CI = 1.28–1.49; P = 4*10−18). The association was independent of calcium levels, hospital‐diagnosed fractures, dementia, and other relevant cofactors. In genetic analysis, participants carrying more vitamin D–increasing variants had a reduced likelihood of incident delirium diagnosis (HR = .80 per standard deviation increase in genetically instrumented vitamin D: .73–.87; P = 2*10−7). CONCLUSION Progressively lower vitamin D levels predicted increased risks of incident hospital‐diagnosed delirium, and genetic evidence supports a shared causal pathway. Because low vitamin D levels are simple to detect and inexpensive and safe to correct, an intervention trial to confirm these results is urgently needed.en_GB
dc.description.sponsorshipAlzheimer’s Societyen_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.description.sponsorshipNational Institute on Agingen_GB
dc.identifier.citationPublished online 5 October 2020en_GB
dc.identifier.doi10.1111/jgs.16853
dc.identifier.grantnumberAS‐JF‐16b‐007en_GB
dc.identifier.grantnumberMR/M023095/1en_GB
dc.identifier.grantnumberNIA R24AG054259 ‐ NIDUS subaward 9581en_GB
dc.identifier.urihttp://hdl.handle.net/10871/123114
dc.language.isoenen_GB
dc.publisherWiley / American Geriatrics Societyen_GB
dc.rights© 2020 The Authors. Journal of the American Geriatrics Society published by Wiley Periodicals LLC on behalf of The American Geriatrics Society. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectdeliriumen_GB
dc.subjectvitamin Den_GB
dc.subjectrisk factoren_GB
dc.subjectbiomarkeren_GB
dc.subjectgeneticen_GB
dc.titleLow Vitamin D Levels and Risk of Incident Delirium in 351,000 Older UK Biobank Participantsen_GB
dc.typeArticleen_GB
dc.date.available2020-10-06T12:46:52Z
dc.identifier.issn0002-8614
exeter.article-numberjgs.16853en_GB
dc.descriptionThis is the final version. Available on open access from Wiley via the DOI in this recorden_GB
dc.identifier.journalJournal of the American Geriatrics Societyen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2020-08-27
exeter.funder::University of Connecticuten_GB
exeter.funder::National Institutes of Healthen_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2020-08-27
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-10-06T12:44:36Z
refterms.versionFCDVoR
refterms.dateFOA2020-10-06T12:46:59Z
refterms.panelAen_GB


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© 2020 The Authors. Journal of the American Geriatrics Society published by Wiley Periodicals LLC on behalf of The American Geriatrics Society.

This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's licence is described as © 2020 The Authors. Journal of the American Geriatrics Society published by Wiley Periodicals LLC on behalf of The American Geriatrics Society. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.