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dc.contributor.authorAltintas, Ayse
dc.contributor.authorBenbir, Gulcin
dc.contributor.authorDemir, Mustafa
dc.contributor.authorPurisa, Sevim
dc.contributor.authorSaruhan-Direskeneli, Guher
dc.date.accessioned2021-03-03T14:36:23Z
dc.date.available2021-03-03T14:36:23Z
dc.identifier.citationAltintas A., Saruhan-Direskeneli G., Benbir G., Demir M., Purisa S., "The role of osteopontin: A shared pathway in the pathogenesis of multiple sclerosis and osteoporosis?", JOURNAL OF THE NEUROLOGICAL SCIENCES, cilt.276, ss.41-44, 2009
dc.identifier.issn0022-510X
dc.identifier.othervv_1032021
dc.identifier.otherav_3a7c9d54-0ffd-448b-9ab7-a140c9e839ec
dc.identifier.urihttp://hdl.handle.net/20.500.12627/43284
dc.identifier.urihttps://doi.org/10.1016/j.jns.2008.08.031
dc.description.abstractOsteopontin (OPN) Was Suggested to have a role in the pathophysiology of MS and in bone metabolism. However, we formerly reported increased presence of osteoporosis in MS patients independent of corticosteroid treatment, there is only limited information about the mechanism of bone loss. In this study, we investigated the role of OPN on bone mineral density in MS patients. Thirty-three relapsing-remitting (RR), 12 secondary progressive (SP), and 5 primary progressive (PP) MS patients and 30 healthy controls were prospectively enrolled. Students' t test, chi-square test, and Pearson correlations were used. The mean OPN level was 155.4 +/- 81.8 ng/ml in controls, and 15.9 +/- 36.2 ng/ml in MS patients (p<0.001).No statistical difference was observed among RR, SP and PPMS patients (p=0.162). No relationship was found between OPN levels and age at onset of disease (p=0.830), gender (p=0.785), IVIS subtypes (p=0.330), disease duration (p=0.744), or EDSS scores (p=0.633).About 34% of IVIS patients versus 10.3% of controls had osteoporosis (p=0.017).Osteopontin levels showed no significant correlation with osteoporosis in controls, but were lower in MS patients with osteoporosis in femur neck (r=0.85, p=0.010).The cumulative dose of corticosteroid treatment did not correlate with OPN levels (p=0.285). In conclusion, our results suggest that OPN may have a role as a shared cytokine in pathogenesis of IVIS and osteoporosis. (C) 2008 Elsevier B.V. All rights reserved.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSinirbilim ve Davranış
dc.subjectNEUROSCIENCES
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleThe role of osteopontin: A shared pathway in the pathogenesis of multiple sclerosis and osteoporosis?
dc.typeMakale
dc.relation.journalJOURNAL OF THE NEUROLOGICAL SCIENCES
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume276
dc.identifier.startpage41
dc.identifier.endpage44
dc.contributor.firstauthorID26426


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