Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/50740
Campo DC Valoridioma
dc.contributor.authorSosa, M.en_US
dc.contributor.authorJódar, E.en_US
dc.contributor.authorSaavedra, P.en_US
dc.contributor.authorNavarro, M. C.en_US
dc.contributor.authorGómez de Tejada, M. J.en_US
dc.contributor.authorMartín, A.en_US
dc.contributor.authorPeña, P.en_US
dc.contributor.authorGómez, J.en_US
dc.date.accessioned2018-11-24T18:28:36Z-
dc.date.available2018-11-24T18:28:36Z-
dc.date.issued2008en_US
dc.identifier.issn0953-6205en_US
dc.identifier.urihttp://hdl.handle.net/10553/50740-
dc.description.abstractBackground: Daily doses higher than 7.5 mg/daily of prednisone or equivalents confer a great risk of vertebral and hip fractures with a clear dose dependence of fracture risk. Information regarding the utility in assessing trabecular bone mineral density by quantitative computer tomography (QCT) in these patients, either in the Canaries or in Spain, is lacking. Moreover, in this setting, the importance of secondary hyperparathyroidism is still controversial.Design, patients and methods: Cross-sectional observational study performed on 1177 consecutive Canary postmenopausal women who attended our Bone Metabolic Unit. The Patient Group was composed of 88 postmenopausal women who were taking oral corticosteroids in dose higher than 7.5 mg/day of prednisone or equivalent for more than 6 months (OG group). The Control Group included 838 postmenopausal women who did not take steroids. A complete validated questionnaire for osteoporosis risk assessment and a complete physical examination were performed. A lateral X-ray of the spine was performed on every woman. Bone mineral density (BMD) was measured at the lumbar spine (LS) by dual X-ray Absorptiometry (DXA) and QCT and at the femoral neck by DXA. Fasting serum and 24 hour urine was collected and biochemical markers of bone remodelling were studied.Results: Both groups were comparable in general characteristics and calcium intake. The OG group showed lower values of BMD estimated both by DXA and QCT (p<0.05). LS BMD was closely correlated by using both methods (r=0.636, p<0.001). The OG group showed lower values of osteocalcin (p=0.023) and TRAP (p=0.026) without significant differences in PTH. Patients in OG group had a higher prevalence of vertebral fractures than controls (13.3% vs 8.6%; crude values: p = 0.049, OR: 1.63 (0.99-2.67); age adjusted: p = 0.003, OR 2.29 (1.33-9.93)).Conclusions: In postmenopausal Canarian women, chronic glucocorticoid therapy is associated with low bone mineral density, measured either by DXA or QCT, with evidence of low turnover and high prevalence of fractures without significant changes in PTH. DXA and QCT provide similar information in the assessment of this high risk population.en_US
dc.languageengen_US
dc.relation.ispartofEuropean Journal of Internal Medicineen_US
dc.sourceEuropean Journal of Internal Medicine[ISSN 0953-6205],v. 19, p. 51-56en_US
dc.subject32 Ciencias médicasen_US
dc.subject3205 Medicina internaen_US
dc.subject.otherInduced Osteoporosisen_US
dc.subject.otherEpidemiologyen_US
dc.subject.otherPathogenesisen_US
dc.subject.otherMulticenteren_US
dc.subject.otherRadiographyen_US
dc.subject.otherManagementen_US
dc.subject.otherDiagnosisen_US
dc.subject.otherTherapyen_US
dc.subject.otherUpdateen_US
dc.subject.otherRisken_US
dc.titlePostmenopausal Canarian women receiving oral glucocorticoids have an increased prevalence of vertebral fractures and low values of bone mineral density measured by quantitative computer tomography and dual X-ray absorptiometry, without significant changes in parathyroid hormoneen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ejim.2007.08.005en_US
dc.identifier.scopus38349174168-
dc.identifier.isi000253274400009-
dc.contributor.authorscopusid7004134221-
dc.contributor.authorscopusid6603967088-
dc.contributor.authorscopusid56677724200-
dc.contributor.authorscopusid7201561727-
dc.contributor.authorscopusid6507688533-
dc.contributor.authorscopusid57214159530-
dc.contributor.authorscopusid57199495248-
dc.contributor.authorscopusid57206360534-
dc.contributor.authorscopusid7004962112-
dc.contributor.authorscopusid24536673300-
dc.contributor.authorscopusid25929188100-
dc.description.lastpage56en_US
dc.description.firstpage51en_US
dc.relation.volume19en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid574595-
dc.contributor.daisngid385681-
dc.contributor.daisngid8838450-
dc.contributor.daisngid1482785-
dc.contributor.daisngid4312290-
dc.contributor.daisngid22097184-
dc.contributor.daisngid12531109-
dc.contributor.daisngid17536156-
dc.description.numberofpages6en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Sosa, M-
dc.contributor.wosstandardWOS:Jodar, E-
dc.contributor.wosstandardWOS:Saavedra, P-
dc.contributor.wosstandardWOS:Navarro, MC-
dc.contributor.wosstandardWOS:de Tejada, MJG-
dc.contributor.wosstandardWOS:Martin, A-
dc.contributor.wosstandardWOS:Pena, P-
dc.contributor.wosstandardWOS:Gomez, J-
dc.date.coverdateEnero 2008en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr1,045-
dc.description.jcrqQ3-
dc.description.scieSCIE-
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR SIANI: Ingeniería biomédica aplicada a estimulación neural y sensorial-
crisitem.author.deptIU Sistemas Inteligentes y Aplicaciones Numéricas-
crisitem.author.orcid0000-0001-6845-2933-
crisitem.author.parentorgIU Sistemas Inteligentes y Aplicaciones Numéricas-
crisitem.author.fullNameSosa Henríquez,Manuel José-
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