Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/33976
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dc.contributor.authorAbtahi, Shahab-
dc.contributor.authorDriessen, Johanna H. M.-
dc.contributor.authorBurden, Andrea M.-
dc.contributor.authorSouverein, Patrick C.-
dc.contributor.authorVAN DEN BERGH, Joop-
dc.contributor.authorvan Staa, Tjeerd P.-
dc.contributor.authorBoonen, Annelies-
dc.contributor.authorde Vries, Frank-
dc.date.accessioned2021-04-26T08:00:58Z-
dc.date.available2021-04-26T08:00:58Z-
dc.date.issued2021-
dc.date.submitted2021-04-13T09:57:42Z-
dc.identifier.citationANNALS OF THE RHEUMATIC DISEASES, 80 (4) , p. 423 -431-
dc.identifier.issn0003-4967-
dc.identifier.urihttp://hdl.handle.net/1942/33976-
dc.description.abstractBackground Patients with rheumatoid arthritis (RA) commonly use oral glucocorticoids (GCs) and proton pump inhibitors (PPIs), both associated with osteoporotic fractures. We investigated the association between concomitant use of oral GCs and PPIs and the risk of osteoporotic fractures among patients with RA. Methods This was a cohort study including patients with RA aged 50+ years from the Clinical Practice Research Datalink between 1997 and 2017. Exposure to oral GCs and PPIs was stratified by the most recent prescription as current use (<6 months), recent use (7-12 months) and past use (>1 year); average daily and cumulative dose; and duration of use. The risk of incident osteoporotic fractures (including hip, vertebrae, humerus, forearm, pelvis and ribs) was estimated by time-dependent Cox proportional-hazards models, statistically adjusted for lifestyle parameters, comorbidities and comedications. Results Among 12 351 patients with RA (mean age of 68 years, 69% women), 1411 osteoporotic fractures occurred. Concomitant current use of oral GCs and PPIs was associated with a 1.6-fold increased risk of osteoporotic fractures compared with non-use (adjusted HR: 1.60, 95% CI: 1.35 to 1.89). This was statistically different from a 1.2-fold increased osteoporotic fracture risk associated with oral GC or PPI use alone. Most individual fracture sites were significantly associated with concomitant use of oral GCs and PPIs. Among concomitant users, fracture risk did not increase with higher daily dose or duration of PPI use. Conclusions There was an interaction in the risk of osteoporotic fractures with concomitant use of oral GCs and PPIs. Fracture risk assessment could be considered when a patient with RA is co-prescribed oral GCs and PPIs.-
dc.description.sponsorshipThe authors would like to acknowledge Keele University's Prognosis and Consultation Epidemiology Research Group who have given us permission to use the morbidity definitions/categorisations lists ((c) 2014). The copyright of the morbidity definitions/categorisations lists ((c) 2014) used in this paper is owned by Keele University, the development of which was supported by the Primary Care Research Consortium. For access/details relating to the morbidity definitions/categorisation lists ((c) 2014), please go to www.keele.ac.uk/mrr.The authors would also like to acknowledge Ard van Veelen from Maastricht University Medical Centre for double--checking the accuracy of tables and figures.-
dc.language.isoen-
dc.publisherBMJ PUBLISHING GROUP-
dc.rightsAuthor(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.-
dc.subject.otherepidemiology-
dc.subject.otherglucocorticoids-
dc.subject.otherosteoporosis-
dc.subject.otherrheumatoid arthritis-
dc.subject.otherAged-
dc.subject.otherCohort Studies-
dc.subject.otherFemale-
dc.subject.otherGlucocorticoids-
dc.subject.otherHumans-
dc.subject.otherMale-
dc.subject.otherProton Pump Inhibitors-
dc.subject.otherRisk Factors-
dc.subject.otherArthritis, Rheumatoid-
dc.subject.otherOsteoporotic Fractures-
dc.titleConcomitant use of oral glucocorticoids and proton pump inhibitors and risk of osteoporotic fractures among patients with rheumatoid arthritis: a population-based cohort study-
dc.typeJournal Contribution-
dc.identifier.epage431-
dc.identifier.issue4-
dc.identifier.spage423-
dc.identifier.volume80-
local.format.pages9-
local.bibliographicCitation.jcatA1-
dc.description.notesde Vries, F (corresponding author), Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Pharmacoepidemiol & Clin Pharmacol, POB 80082, NL-3508 TB Utrecht, Netherlands.-
dc.description.notesf.devries@uu.nl-
dc.description.otherde Vries, F (corresponding author), Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Pharmacoepidemiol & Clin Pharmacol, POB 80082, NL-3508 TB Utrecht, Netherlands. f.devries@uu.nl-
local.publisher.placeBRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1136/annrheumdis-2020-218758-
dc.identifier.pmid33310727-
dc.identifier.isiWOS:000629185200020-
dc.contributor.orcidde Vries, Frank/0000-0003-3837-8319; /0000-0001-7082-8530; Abtahi,-
dc.contributor.orcidShahab/0000-0003-0482-5563; van Staa, Tjeerd/0000-0001-9363-742X-
dc.identifier.eissn1468-2060-
local.provider.typewosris-
local.uhasselt.uhpubyes-
local.description.affiliation[Abtahi, Shahab; Driessen, Johanna H. M.; Burden, Andrea M.; de Vries, Frank] Maastricht Univ, Med Ctr, Dept Clin Pharm & Toxicol, Maastricht, Netherlands.-
local.description.affiliation[Abtahi, Shahab; Driessen, Johanna H. M.; Souverein, Patrick C.; van Staa, Tjeerd P.; de Vries, Frank] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Pharmacoepidemiol & Clin Pharmacol, POB 80082, NL-3508 TB Utrecht, Netherlands.-
local.description.affiliation[Abtahi, Shahab; Driessen, Johanna H. M.; de Vries, Frank] Maastricht Univ, Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands.-
local.description.affiliation[Driessen, Johanna H. M.] Maastricht Univ, Med Ctr, NUTRIM Sch Nutr & Translat Res Metab, Maastricht, Netherlands.-
local.description.affiliation[Burden, Andrea M.] Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Inst Pharmaceut Sci, Zurich, Switzerland.-
local.description.affiliation[van den Bergh, Joop P.; Boonen, Annelies] Maastricht Univ, Med Ctr, Div Rheumatol, Dept Internal Med, Maastricht, Netherlands.-
local.description.affiliation[van den Bergh, Joop P.] Hasselt Univ, Fac Med & Life Sci, Hasselt, Belgium.-
local.description.affiliation[van den Bergh, Joop P.] VieCuri Med Ctr, Dept Internal Med, Venlo, Netherlands.-
local.description.affiliation[van Staa, Tjeerd P.] Univ Manchester, Fac Biol Med & Hlth, Div Informat Imaging & Data Sci, Ctr Hlth Informat,Sch Hlth Sci, Manchester, Lancs, England.-
local.description.affiliation[Boonen, Annelies] Maastricht Univ, Care & Publ Hlth Res Inst CAPHRI, Maastricht, Netherlands.-
local.description.affiliation[de Vries, Frank] Southampton Gen Hosp, MRC Epidemiol Lifecourse Unit, Southampton, Hants, England.-
local.uhasselt.internationalyes-
item.fullcitationAbtahi, Shahab; Driessen, Johanna H. M.; Burden, Andrea M.; Souverein, Patrick C.; VAN DEN BERGH, Joop; van Staa, Tjeerd P.; Boonen, Annelies & de Vries, Frank (2021) Concomitant use of oral glucocorticoids and proton pump inhibitors and risk of osteoporotic fractures among patients with rheumatoid arthritis: a population-based cohort study. In: ANNALS OF THE RHEUMATIC DISEASES, 80 (4) , p. 423 -431.-
item.fulltextWith Fulltext-
item.accessRightsOpen Access-
item.contributorAbtahi, Shahab-
item.contributorDriessen, Johanna H. M.-
item.contributorBurden, Andrea M.-
item.contributorSouverein, Patrick C.-
item.contributorVAN DEN BERGH, Joop-
item.contributorvan Staa, Tjeerd P.-
item.contributorBoonen, Annelies-
item.contributorde Vries, Frank-
item.validationecoom 2022-
crisitem.journal.issn0003-4967-
crisitem.journal.eissn1468-2060-
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