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dc.contributor.authorKiyokawa, Hirofumien
dc.contributor.authorMuro, Shigeoen
dc.contributor.authorOguma, Tsuyoshien
dc.contributor.authorSato, Susumuen
dc.contributor.authorTanabe, Naoyaen
dc.contributor.authorTakahashi, Tamakien
dc.contributor.authorKudo, Megumien
dc.contributor.authorKinose, Daisukeen
dc.contributor.authorKondoh, Hiroshien
dc.contributor.authorKubo, Takeshien
dc.contributor.authorHoshino, Yumaen
dc.contributor.authorOgawa, Emikoen
dc.contributor.authorHirai, Toyohiroen
dc.contributor.authorMishima, Michiakien
dc.contributor.alternative室, 繁郎ja
dc.date.accessioned2012-10-19T06:35:25Z-
dc.date.available2012-10-19T06:35:25Z-
dc.date.issued2012-06-
dc.identifier.issn1541-2563-
dc.identifier.urihttp://hdl.handle.net/2433/160226-
dc.description.abstractBackground: COPD pathology involves not only the lungs but also extrapulmonary abnormalities. Osteoporosis is one of the most important abnormalities because it may cause vertebral compression fractures and deteriorate pulmonary function. COPD patients have many risk factors for osteoporosis, such as low BMI, decreased activity, systemic infl ammation, and use of corticosteroids. Some of these factors have been shown to deteriorate with COPD exacerbations. We previously demonstrated the correlation between emphysema and osteoporosis and between emphysema progression and COPD exacerbations. Thus, the hypothesis that exacerbation causes osteoporosis progression in COPD patients was investigated. Methods: Forty-two COPD patients not on osteoporosis treatment for over 2 years were recruited. During follow-up, exacerbations had been prospectively recorded. Thoracic vertebral bone mineral density (BMD) was measured using chest CT, and the annual change in BMD was calculated. The change was compared between patients with and without a history of exacerbations. Results: The decrease in thoracic vertebral BMD was greater in patients with than in those without a history of exacerbations (median ΔBMD mg/ml⋅year: –3.78 versus –0.30, p = 0.02). Moreover, multivariate regression analysis showed that exacerbations and baseline PaO 2 were independent predictors of the BMD decrease (R 2 = 0.20, p = 0.007, and R 2 = 0.09, p = 0.03, respectively) after adjustment for baseline age, smoking status, and airfl ow limitation. Conclusions: This is the fi rst longitudinal study to demonstrate that COPD exacerbations are independently associated with osteoporosis progression. Osteoporosis progression should be evaluated in COPD patients, especially in those with a history of frequent exacerbations.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherInforma Healthcareen
dc.rights© Informa Healthcare USA, Inc.en
dc.subjectExacerbationen
dc.subjectOsteoporosisen
dc.subjectBone mineral densityen
dc.subjectChronic obstmetive pulmonary diseaseen
dc.subjectEmphysemaen
dc.subject.meshAdrenal Cortex Hormones/adverse effectsen
dc.subject.meshAgeden
dc.subject.meshAnti-Inflammatory Agents/adverse effectsen
dc.subject.meshBody Mass Indexen
dc.subject.meshBone Densityen
dc.subject.meshDisease Progressionen
dc.subject.meshFemaleen
dc.subject.meshHumansen
dc.subject.meshLongitudinal Studiesen
dc.subject.meshMaleen
dc.subject.meshMiddle Ageden
dc.subject.meshOsteoporosis/complicationsen
dc.subject.meshOsteoporosis/radiographyen
dc.subject.meshPulmonary Disease, Chronic Obstructive/complicationsen
dc.subject.meshPulmonary Disease, Chronic Obstructive/radiographyen
dc.subject.meshPulmonary Emphysema/complicationsen
dc.subject.meshPulmonary Emphysema/radiographyen
dc.subject.meshRadiography, Thoracicen
dc.subject.meshRisk Factorsen
dc.subject.meshSmokingen
dc.subject.meshThoracic Vertebrae/radiographyen
dc.subject.meshTomography, X-Ray Computeden
dc.titleImpact of COPD exacerbations on osteoporosis assessed by chest CT scan.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleCOPD: Journal of Chronic Obstructive Pulmonary Diseaseen
dc.identifier.volume9-
dc.identifier.issue3-
dc.identifier.spage235-
dc.identifier.epage242-
dc.relation.doi10.3109/15412555.2011.650243-
dc.textversionpublisher-
dc.identifier.pmid22360380-
dcterms.accessRightsopen access-
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