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Increase in non-transferrin bound iron and the oxidative stress status in epilepsy patients treated using valproic acid monotherapy

dc.contributor.authorS. Ounjaijeanen_US
dc.contributor.authorT. Westermarcken_US
dc.contributor.authorM. Partinenen_US
dc.contributor.authorE. Plonka-Poltoraken_US
dc.contributor.authorP. Kaipainenen_US
dc.contributor.authorM. Kaskien_US
dc.contributor.authorS. Fucharoenen_US
dc.contributor.authorS. Srichairatanakoolen_US
dc.contributor.authorF. Atroshien_US
dc.contributor.otherHelsingin Yliopistoen_US
dc.contributor.otherChiang Mai Universityen_US
dc.contributor.otherRinnekoti Foundation Finlanden_US
dc.contributor.otherProvincial Hospital, Rzeszowen_US
dc.contributor.otherThe Institute of Science and Technology for Research and Development, Mahidol Universityen_US
dc.date.accessioned2018-05-03T08:33:57Z
dc.date.available2018-05-03T08:33:57Z
dc.date.issued2011-04-01en_US
dc.description.abstractObjective: This study aims to investigate the alteration of iron homeostasis and oxidative stress status in epilepsy patients treated with valproic acid (VPA) monotherapy. Materials: 24 epilepsy patients receiving VPA monotherapy (12 men, 12 women, age 27.5 ± 7.2 y) and 24 sex- and age-matched healthy volunteers were included in the study. Methods: The level of iron status parameters; serumiron, ferritin, transferrin saturation, non-transferrin bound iron (NTBI), serum level of trace elements (copper, zinc and selenium), concentration of antioxidant parameters, activities of antioxidant enzymes and level of lipid peroxidation product were determined. Results: NTBI was found in the patients although their other iron status parameters were normal. Levels of antioxidant parameters were decreased while activities of antioxidant enzymes were increased. Levels of serum MDA were significantly increased in patientswith epilepsy. The daily dose of valproic acid associatedwas statistically significant: serumconcentration of NTBI (r = 0.579; p = 0.003) and MDA (r = 0.465; p = 0.022).Apositive correlation existed between NTBI and zinc (r = 0.522; p = 0.009). Conclusion: According to our results, VPA treatment in patients with epilepsy contributes to themetabolism of iron, leading to the formation of NTBI and an increase in oxidative stress. ©2011 Dustri-Verlag Dr. K. Feistle.en_US
dc.identifier.citationInternational Journal of Clinical Pharmacology and Therapeutics. Vol.49, No.4 (2011), 268-276en_US
dc.identifier.doi10.5414/CP201466en_US
dc.identifier.issn09461965en_US
dc.identifier.other2-s2.0-79955949063en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/12581
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955949063&origin=inwarden_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleIncrease in non-transferrin bound iron and the oxidative stress status in epilepsy patients treated using valproic acid monotherapyen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955949063&origin=inwarden_US

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