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dc.contributor.authorGholami, K
dc.contributor.authorTalasaz, AH
dc.contributor.authorEntezari-Maleki, T
dc.contributor.authorSalarifar, M
dc.contributor.authorHadjibabaie, M
dc.contributor.authorJavadi, MR
dc.contributor.authorDousti, S
dc.contributor.authorHamishehkar, H
dc.contributor.authorMaleki, S
dc.date.accessioned2018-08-26T07:27:18Z
dc.date.available2018-08-26T07:27:18Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/46864
dc.description.abstractHigh plasma level of P-selectin is associated with the development of venous thromboembolism (VTE). Furthermore, supplementation of vitamin D could decrease thrombotic events. Hence, this study was designed to examine whether the administration of vitamin D can influence the plasma level of P-selectin in patients with VTE. In the randomized controlled trial, 60 patients with confirmed acute deep vein thrombosis and/or pulmonary embolism (PE) were randomized into the intervention (n = 20) and control (n = 40) groups. The intervention arm was given an intramuscular single dose of 300 000 IU vitamin D-3. Plasma level of 25-hydroxy vitamin D, P-selectin, and high-sensitive C-reactive protein (hs-CRP) was measured at baseline and 4 weeks after. The plasma level of P-selectin (95% confidence interval = -5.99 to -1.63, P = .022) and hs-CRP (P = .024) significantly declined in vitamin D-treated group, while only hs-CRP was significantly decreased in the control group (P = .011). However, the magnitude of these reductions was not statistically significant. This study could not support the potential benefit of the high-dose vitamin D on plasma level of P-selectin and hs-CRP in patients with VTE.
dc.language.isoEnglish
dc.relation.ispartofCLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
dc.subjectvitamin D
dc.subjectP-selectin
dc.subjecths-CRP
dc.subjectthromboembolism
dc.subjectDVT
dc.subjectPE
dc.titleThe Effect of High-Dose Vitamin D-3 on Soluble P-Selectin and hs-CRP Level in Patients With Venous Thromboembolism: A Randomized Clinical Trial
dc.typeArticle
dc.citation.volume22
dc.citation.issue5
dc.citation.spage483
dc.citation.epage489
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1177/1076029614568715


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