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dc.contributor.authorMalek Mahdavi, A
dc.contributor.authorMahdavi, R
dc.contributor.authorKolahi, S
dc.date.accessioned2018-08-26T08:53:27Z
dc.date.available2018-08-26T08:53:27Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/53952
dc.description.abstractObjective: Considering the importance of inflammation in the pathogenesis of osteoarthritis (OA) and induction of pain, this study was aimed to investigate the effect of L-carnitine supplementation on serum inflammatory mediators and OA-associated pain in females with knee OA. Methods: In this clinical trial, 72 females with mild to moderate knee osteoarthritis started the study, divided into 2 groups to receive 750 mg/day L-carnitine (n = 36) or placebo (n = 36) for 8 weeks. Serum levels of Interleukine-1? (IL-1?), high-sensitivity C-reactive protein (hs-CRP), matrix metalloproteinases (MMPs)-1 and -13, and visual analog scale (VAS) for pain were assessed before and after supplementation. Data were analyzed by t test, Wilcoxon signed rank test, Mann-Whitney U test, and analysis of covariance. Results: Only 69 patients (33 in the L-carnitine group and 36 in the placebo group) completed the study. L-Carnitine supplementation decreased serum IL-1? and MMP-1 levels significantly (p = 0.001 and p = 0.021, respectively); however, serum hs-CRP and MMP-13 levels did not change significantly (p > 0.05). In the placebo group, serum IL-1? levels increased significantly (p = 0.011), whereas other studied biomarkers did not change significantly. The mean VAS score decreased significantly in the L-carnitine and placebo groups by 52.67% and 21.82%, respectively (p < 0.001). Significant differences were only observed between the 2 groups in serum IL-1? (p < 0.001) and MMP-1 (p = 0.006) levels and mean VAS score (p = 0.002) after adjusting for baseline values and covariates. Conclusion: Despite observed beneficial effects of short-term supplementation of L-carnitine in decreasing serum inflammatory mediators and improving pain in knee OA patients, further studies are needed to achieve concise conclusions. © 2016, © American College of Nutrition Published by Taylor & Francis Group, LLC.
dc.language.isoEnglish
dc.relation.ispartofJournal of the American College of Nutrition
dc.subjectC reactive protein
dc.subjectcarnitine
dc.subjectcollagenase 3
dc.subjectinterleukin 1beta
dc.subjectinterstitial collagenase
dc.subjectplacebo
dc.subjectantiinflammatory agent
dc.subjectbiological marker
dc.subjectC reactive protein
dc.subjectcarnitine
dc.subjectcollagenase 3
dc.subjectinterleukin 1beta
dc.subjectinterstitial collagenase
dc.subjectmatrix metalloproteinase
dc.subjectadult
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectbody mass
dc.subjectbody weight
dc.subjectcaloric intake
dc.subjectcontrolled study
dc.subjectdiet supplementation
dc.subjectdisease severity assessment
dc.subjectdouble blind procedure
dc.subjectenzyme linked immunosorbent assay
dc.subjectfemale
dc.subjecthuman
dc.subjectinflammation
dc.subjectknee osteoarthritis
dc.subjectmajor clinical study
dc.subjectpain severity
dc.subjectrandomized controlled trial
dc.subjectturbidimetry
dc.subjectvisual analog scale
dc.subjectblood
dc.subjectdietary supplement
dc.subjectinflammation
dc.subjectmiddle aged
dc.subjectOsteoarthritis, Knee
dc.subjectpilot study
dc.subjectAnti-Inflammatory Agents
dc.subjectBiomarkers
dc.subjectC-Reactive Protein
dc.subjectCarnitine
dc.subjectDietary Supplements
dc.subjectDouble-Blind Method
dc.subjectFemale
dc.subjectHumans
dc.subjectInflammation
dc.subjectInterleukin-1beta
dc.subjectMatrix Metalloproteinase 1
dc.subjectMatrix Metalloproteinase 13
dc.subjectMatrix Metalloproteinases
dc.subjectMiddle Aged
dc.subjectOsteoarthritis, Knee
dc.subjectPilot Projects
dc.subjectPlacebos
dc.titleEffects of l-Carnitine Supplementation on Serum Inflammatory Factors and Matrix Metalloproteinase Enzymes in Females with Knee Osteoarthritis: A Randomized, Double-Blind, Placebo-Controlled Pilot Study
dc.typeArticle
dc.citation.volume35
dc.citation.issue7
dc.citation.spage597
dc.citation.epage603
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1080/07315724.2015.1068139


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