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dc.contributor.authorAhmadi, R
dc.contributor.authorHajialilo, M
dc.contributor.authorGhorbanihaghjo, A
dc.contributor.authorMota, A
dc.contributor.authorRaeisi, S
dc.contributor.authorBargahi, N
dc.contributor.authorValilo, M
dc.contributor.authorAskarian, F
dc.date.accessioned2018-08-26T04:59:38Z
dc.date.available2018-08-26T04:59:38Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/38866
dc.description.abstractScleroderma is a chronic connective tissue disease of unknown etiology. Vitamin D and parathyroid hormone (PTH) that play particular functions in calcium and phosphate homeostasis may be involved in the etiology of this disorder. Klotho, the co-receptor of the fibroblast growth factor 23 (FGF-23), can interfere with calcium and phosphate metabolism. The purpose of this study was to evaluate serum Klotho, FGF-23, intact PTH (iPTH) and vitamin D levels in scleroderma patients compared with the healthy controls.The study was performed in Biotechnology Research Center, Tabriz University of Medical Sciences (TUMS) from 2014-2015. Sixty scleroderma patients based on the classification criteria of systemic sclerosis and 30 age- and sex-matched healthy controls were included in this study. Serum Klotho, FGF-23, 25-hydroxy vitamin D (25-OH Vit D), and iPTH levels were analyzed using ELISA.Serum levels of Klotho and 25-OH Vit D in the scleroderma patients were lower than those in the healthy controls (P<0.001). In addition, scleroderma patients had higher serum iPTH levels than the controls (P<0.001). There was no significant difference in serum FGF-23 levels between the patients and controls (P=0.202).The decreased serum Klotho, 25-OH Vit D, and increased iPTH levels in the scleroderma patients may be associated with the pathogenesis of this disease and could be considered a future therapeutic target.
dc.language.isoEnglish
dc.relation.ispartofIranian journal of public health
dc.titleFGF-23, Klotho and Vitamin D Levels in Scleroderma.
dc.typearticle
dc.citation.volume46
dc.citation.issue4
dc.citation.spage530
dc.citation.epage536
dc.citation.indexPubmed


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