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dc.contributor.authorTateuchi, Hiroshigeen
dc.contributor.authorAkiyama, Haruhikoen
dc.contributor.authorGoto, Kojien
dc.contributor.authorSo, Kazutakaen
dc.contributor.authorKuroda, Yutakaen
dc.contributor.authorIchihashi, Noriakien
dc.contributor.alternative建内, 宏重ja
dc.contributor.alternative後藤, 公志ja
dc.contributor.alternative黒田, 隆ja
dc.contributor.alternative市橋, 則明ja
dc.date.accessioned2020-08-04T08:06:11Z-
dc.date.available2020-08-04T08:06:11Z-
dc.date.issued2020-07-
dc.identifier.issn0770-3198-
dc.identifier.urihttp://hdl.handle.net/2433/253577-
dc.description.abstractOBJECTIVES: Recently, several clinical prognostic factors for hip osteoarthritis (OA) progression such as spinal malalignment, reduced spinal mobility, and excessive daily cumulative hip loading have been identified. This study aimed to identify clinical phenotypes based on clinical prognostic factors in patients with secondary hip OA using data from prospective cohort studies and to define the clinical features of each phenotype. METHODS: Fifty patients participated. Two-step cluster analysis was performed to identify the phenotypes using the following potential prognostic factors for hip OA progression: spinal inclination in standing, thoracolumbar spine mobility, daily cumulative hip moment, and minimum joint space width (JSW) at baseline. Comprehensive basic and clinical features (age, body mass index, hip pain, Harris hip score, JSW, radiographic hip morphology, hip impairments, spinal alignment and mobility, and gait-related variables) and ratio of progressors in 12 months were compared among the phenotypes using bootstrap method (unadjusted and adjusted for age). RESULTS: Three phenotypes were identified and each phenotype was characterized as follows (P < 0.05): phenotype 1 (30%)-relatively young age and higher daily cumulative hip loading; phenotype 2 (42.0%)-relatively older age, reduced JSW, and less spinal mobility; and phenotype 3 (28.0%)-changed thoracic spine alignment and less spinal (especially in the thoracic spine) mobility. The ratio of progressors among the phenotypes was not statistically significantly different. These characteristics remained after adjustment for age. CONCLUSION: Three phenotypes with similar progression risk were identified. This finding will help in designing treatment tailored to each phenotype for hip OA progression prevention.Key Points• Three phenotypes with similar progression risk were identified based on clinical prognostic factors.• Phenotype 1 was characterized by young age and higher daily cumulative hip loading.• Phenotype 2 was relatively old age and had reduced JSW and less spinal mobility.• Phenotype 3 had changed thoracic spine alignment and less thoracic spine mobility.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rightsThis is a post-peer-review, pre-copyedit version of an article published in Clinical rheumatology. The final authenticated version is available online at: http://dx.doi.org/10.1007/s10067-020-04988-7.en
dc.rightsThe full-text file will be made open to the public on 10 February 2021 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.rightsThis is not the published version. Please cite only the published version.en
dc.subjectGaiten
dc.subjectHip osteoarthritisen
dc.subjectPhenotypeen
dc.subjectProgressionen
dc.subjectSpineen
dc.titleClinical phenotypes based on clinical prognostic factors in patients with secondary hip osteoarthritis: preliminary findings from a prospective cohort studyen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleClinical rheumatologyen
dc.identifier.volume39-
dc.identifier.spage2207-
dc.identifier.epage2217-
dc.relation.doi10.1007/s10067-020-04988-7-
dc.textversionauthor-
dc.addressDepartment of Preventive Physical Therapy, Human Health Sciences, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Orthopaedic Surgery, School of Medicine, Gifu Universityen
dc.addressDepartment of Orthopaedic Surgery, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Orthopaedic Surgery, Osaka Red Cross Hospitalen
dc.addressDepartment of Orthopaedic Surgery, Graduate School of Medicineen
dc.addressDepartment of Physical Therapy, Human Health Sciences, Graduate School of Medicineen
dc.identifier.pmid32088798-
dcterms.accessRightsopen access-
datacite.date.available2021-02-10-
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