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Effects of glucocorticoids on weight change during the treatment of Wegener's granulomatosis

dc.contributor.authorWung, Peter K.en_US
dc.contributor.authorAnderson, Troyen_US
dc.contributor.authorFontaine, Kevin R.en_US
dc.contributor.authorHoffman, Gary S.en_US
dc.contributor.authorSpecks, Ulrichen_US
dc.contributor.authorMerkel, Peter A.en_US
dc.contributor.authorSpiera, Robert F.en_US
dc.contributor.authorDavis, John C.en_US
dc.contributor.authorSt. Clair, E. Williamen_US
dc.contributor.authorMcCune, William Josephen_US
dc.contributor.authorStone, John H.en_US
dc.date.accessioned2008-06-04T14:36:16Z
dc.date.available2009-06-01T20:08:52Zen_US
dc.date.issued2008-05-15en_US
dc.identifier.citationWung, Peter K.; Anderson, Troy; Fontaine, Kevin R.; Hoffman, Gary S.; Specks, Ulrich; Merkel, Peter A.; Spiera, Robert; Davis, John C.; St.Clair, E. William; McCune, W. Joseph; Stone, John H. (2008). "Effects of glucocorticoids on weight change during the treatment of Wegener's granulomatosis." Arthritis & Rheumatism 59(5): 746-753. <http://hdl.handle.net/2027.42/58632>en_US
dc.identifier.issn0004-3591en_US
dc.identifier.issn1529-0131en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/58632
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18438908&dopt=citationen_US
dc.description.abstractObjective Weight gain is a side effect of glucocorticoid (GC) use, but the natural history and health implications of changes in weight that occur during the treatment of inflammatory disease are not understood. Methods We evaluated data from the Wegener's Granulomatosis Etanercept Trial. Patients were categorized according to clinical outcome at 1 year: remission (no disease flares), single flare, or multiple flares. Risk factors for gaining ≥10 kg were examined in multivariate models. Results Weights at baseline and 1 year were available for 157 (93%) of the 168 patients analyzed. During year 1, the mean cumulative prednisone dosage in the multiple flares subgroup was 7.9 gm, compared with 6.0 gm and 3.9 gm in the single flare and remission subgroups, respectively ( P < 0.001). Patients in these subgroups gained an average of 2.6 kg, 4.1 kg, and 5.8 kg, respectively ( P = 0.005). Weight gain did not correlate with cumulative GC dose (R = 0.10, P = 0.25). Thirty-five patients (22.3%) gained and maintained ≥10 kg in the first year. New diagnosis of Wegener's granulomatosis at baseline was an independent predictor of gaining ≥10 kg at 1 year (odds ratio 19.7, 95% confidence interval 2.4–162.6, P = 0.006). Among the 78 patients in the remission subgroup, 40 sustained remissions through the 2-year time point. For these 40 patients, the mean weight gained at year 1 did not regress by the end of year 2, despite the absence of continued GC use. Conclusion Disease control was associated with lower cumulative GC doses but greater weight gain. More than one-fifth of patients gained >10 kg in the first year of treatment. The quantity of weight gained by patients during treatment has potential future health implications.en_US
dc.format.extent290087 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
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dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.titleEffects of glucocorticoids on weight change during the treatment of Wegener's granulomatosisen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeriatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arboren_US
dc.contributor.affiliationotherJohns Hopkins University School of Medicine, Baltimore, Maryland ; Dr. Wung and Mr. Anderson contributed equally to this work.en_US
dc.contributor.affiliationotherJohns Hopkins University School of Medicine, Baltimore, Marylanden_US
dc.contributor.affiliationotherJohns Hopkins University School of Medicine, Baltimore, Marylanden_US
dc.contributor.affiliationotherCleveland Clinic Foundation, Cleveland, Ohioen_US
dc.contributor.affiliationotherMayo Clinic, Rochester, Minnesotaen_US
dc.contributor.affiliationotherBoston University School of Medicine, Boston, Massachusettsen_US
dc.contributor.affiliationotherBeth Israel Medical Center, New York, New Yorken_US
dc.contributor.affiliationotherUniversity of California at San Franciscoen_US
dc.contributor.affiliationotherDuke University Medical Center, Durham, North Carolina ; Dr. St.Clair received consultant fees, speaking fees, and/or honoraria (less than $10,000 each) from Genentech, Medimmune, Human Genome Sciences, Novartis, and Bristol-Meyers Squibb.en_US
dc.contributor.affiliationotherJohns Hopkins University School of Medicine, Baltimore, Maryland ; Rheumatic Diseases Unit, Massachusetts General Hospital, 55 Fruit Street, Yawkey Center 2C, Boston, MA 02114en_US
dc.identifier.pmid18438908en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/58632/1/23561_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/art.23561en_US
dc.identifier.sourceArthritis & Rheumatismen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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