AB0510 Alphacalcidol Therapy Decreases GSH, SOD and Catalase Levels in Erythrocytes of Rheumatoid Arthritis Patients
BackgroundLow vitamin D serum levels have been associated with several autoimmune diseases including rheumatoid arthritis (RA). Vitamin D deficiency enhances oxidative stress that plays a substantial role in pathogenesis of autoimmune diseases.ObjectivesBecause erythrocytes are extremly vulnerabile...
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description | BackgroundLow vitamin D serum levels have been associated with several autoimmune diseases including rheumatoid arthritis (RA). Vitamin D deficiency enhances oxidative stress that plays a substantial role in pathogenesis of autoimmune diseases.ObjectivesBecause erythrocytes are extremly vulnerabile to oxidative stress, the aim of this research was to analyse the effect of twelve weeks long alphacalcidol therapy in patients with RA on erythrocytes' glutathione (GSH), superoxide dismutase (SOD) and catalase levels, as an oxidative stress markers.MethodsIn ten patients with active RA (DAS28(SE) score >3.2) of both sexes, age 53.78±12.01 alphacalcidol (2μg/day) was added to previously applied therapy (stable dose of methotrexate, without any steroid therapy) during three months. Blood samples were taken before and after 12 weeks of alphacalcidol therapy. GSH, SOD and catalase levels in isolated and lysed erythrocytes were determined mannualy, using spectrophotometry method. Hemoglobin (Hb) levels were measured in lysed erythrocytes using biochemical analyser (Beckman coulter AcT diff) and levels expressed as μmol/g Hb for GSH and U/g Hb for catalase and SOD. In addition, parameters of inflammation (serum C-reactive protein (CRP) and sedimentation rate (SE)) were determined and disease activity was assessed using DAS28 (SE) score. Laboratory safety assessment of the study drug was evaluated monthly. Student's t-test was used for statistical analysis.ResultsAverage erythrocytes GSH level before treatment was 6.0±2.3 μmol/g Hb and it decreased to 3.7±1.3 μmol/g Hb (p=0.02) after treatment. Futhermore, initial catalase levels of 1412.3±840.2 U/ g Hb dropped to 211.3±119.1 U/g Hb (p=0.01) after twelve weeks of alphacalcidol therapy. Although slight reduction in SOD levels was observed after therapy, it was statistically insignificant. Significant clinical impovement was observed, DAS28(SE) was before treatment 5.81±0.89 and decreased to 4.31±1.03 (p=0.001), and CRP level of 28.41±28.16 dropped to 10.03±11.68 (p=0.000).ConclusionsDecreased levels of erythrocytes' GSH and catalase in RA patients after 12 weeks of alphacalcidol therapy indicate that alphacalcidol induced antioxidative effect. We assume that alphacalcidol lead to reduction of H2O2 production in erythrocytes and therefore decreased the need for antioxidative enzymes catalase and glutathione peroxidase activity. Antioxidative effect of alphacalcidol was in line with good clinical outcome in patients.Disc |
doi_str_mv | 10.1136/annrheumdis-2015-eular.3365 |
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Vitamin D deficiency enhances oxidative stress that plays a substantial role in pathogenesis of autoimmune diseases.ObjectivesBecause erythrocytes are extremly vulnerabile to oxidative stress, the aim of this research was to analyse the effect of twelve weeks long alphacalcidol therapy in patients with RA on erythrocytes' glutathione (GSH), superoxide dismutase (SOD) and catalase levels, as an oxidative stress markers.MethodsIn ten patients with active RA (DAS28(SE) score >3.2) of both sexes, age 53.78±12.01 alphacalcidol (2μg/day) was added to previously applied therapy (stable dose of methotrexate, without any steroid therapy) during three months. Blood samples were taken before and after 12 weeks of alphacalcidol therapy. GSH, SOD and catalase levels in isolated and lysed erythrocytes were determined mannualy, using spectrophotometry method. Hemoglobin (Hb) levels were measured in lysed erythrocytes using biochemical analyser (Beckman coulter AcT diff) and levels expressed as μmol/g Hb for GSH and U/g Hb for catalase and SOD. In addition, parameters of inflammation (serum C-reactive protein (CRP) and sedimentation rate (SE)) were determined and disease activity was assessed using DAS28 (SE) score. Laboratory safety assessment of the study drug was evaluated monthly. Student's t-test was used for statistical analysis.ResultsAverage erythrocytes GSH level before treatment was 6.0±2.3 μmol/g Hb and it decreased to 3.7±1.3 μmol/g Hb (p=0.02) after treatment. Futhermore, initial catalase levels of 1412.3±840.2 U/ g Hb dropped to 211.3±119.1 U/g Hb (p=0.01) after twelve weeks of alphacalcidol therapy. Although slight reduction in SOD levels was observed after therapy, it was statistically insignificant. Significant clinical impovement was observed, DAS28(SE) was before treatment 5.81±0.89 and decreased to 4.31±1.03 (p=0.001), and CRP level of 28.41±28.16 dropped to 10.03±11.68 (p=0.000).ConclusionsDecreased levels of erythrocytes' GSH and catalase in RA patients after 12 weeks of alphacalcidol therapy indicate that alphacalcidol induced antioxidative effect. We assume that alphacalcidol lead to reduction of H2O2 production in erythrocytes and therefore decreased the need for antioxidative enzymes catalase and glutathione peroxidase activity. Antioxidative effect of alphacalcidol was in line with good clinical outcome in patients.Disclosure of InterestNone declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2015-eular.3365</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>Kidlington: Elsevier Limited</publisher><ispartof>Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.1069</ispartof><rights>2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2015 (c) 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/74/Suppl_2/1069.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/74/Suppl_2/1069.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77569,77600</link.rule.ids></links><search><creatorcontrib>Zivanovic Radnic, T.</creatorcontrib><creatorcontrib>Simic-Pasalic, K.</creatorcontrib><creatorcontrib>Sefik-Bukilica, M.</creatorcontrib><creatorcontrib>Misirlic Dencic, S.</creatorcontrib><creatorcontrib>Stojkovic, T.</creatorcontrib><creatorcontrib>Damjanov, N.</creatorcontrib><creatorcontrib>Vojinovic, J.</creatorcontrib><title>AB0510 Alphacalcidol Therapy Decreases GSH, SOD and Catalase Levels in Erythrocytes of Rheumatoid Arthritis Patients</title><title>Annals of the rheumatic diseases</title><description>BackgroundLow vitamin D serum levels have been associated with several autoimmune diseases including rheumatoid arthritis (RA). Vitamin D deficiency enhances oxidative stress that plays a substantial role in pathogenesis of autoimmune diseases.ObjectivesBecause erythrocytes are extremly vulnerabile to oxidative stress, the aim of this research was to analyse the effect of twelve weeks long alphacalcidol therapy in patients with RA on erythrocytes' glutathione (GSH), superoxide dismutase (SOD) and catalase levels, as an oxidative stress markers.MethodsIn ten patients with active RA (DAS28(SE) score >3.2) of both sexes, age 53.78±12.01 alphacalcidol (2μg/day) was added to previously applied therapy (stable dose of methotrexate, without any steroid therapy) during three months. Blood samples were taken before and after 12 weeks of alphacalcidol therapy. GSH, SOD and catalase levels in isolated and lysed erythrocytes were determined mannualy, using spectrophotometry method. Hemoglobin (Hb) levels were measured in lysed erythrocytes using biochemical analyser (Beckman coulter AcT diff) and levels expressed as μmol/g Hb for GSH and U/g Hb for catalase and SOD. In addition, parameters of inflammation (serum C-reactive protein (CRP) and sedimentation rate (SE)) were determined and disease activity was assessed using DAS28 (SE) score. Laboratory safety assessment of the study drug was evaluated monthly. Student's t-test was used for statistical analysis.ResultsAverage erythrocytes GSH level before treatment was 6.0±2.3 μmol/g Hb and it decreased to 3.7±1.3 μmol/g Hb (p=0.02) after treatment. Futhermore, initial catalase levels of 1412.3±840.2 U/ g Hb dropped to 211.3±119.1 U/g Hb (p=0.01) after twelve weeks of alphacalcidol therapy. Although slight reduction in SOD levels was observed after therapy, it was statistically insignificant. Significant clinical impovement was observed, DAS28(SE) was before treatment 5.81±0.89 and decreased to 4.31±1.03 (p=0.001), and CRP level of 28.41±28.16 dropped to 10.03±11.68 (p=0.000).ConclusionsDecreased levels of erythrocytes' GSH and catalase in RA patients after 12 weeks of alphacalcidol therapy indicate that alphacalcidol induced antioxidative effect. We assume that alphacalcidol lead to reduction of H2O2 production in erythrocytes and therefore decreased the need for antioxidative enzymes catalase and glutathione peroxidase activity. Antioxidative effect of alphacalcidol was in line with good clinical outcome in patients.Disclosure of InterestNone declared</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqVkL9OwzAQxi0EEqXwDpa6EvDFsZOIKbSlRapURMtsObGjpEqTYKeVsrHwojwJDmVgZTrd3ffdnx9CEyB3AJTfy7o2hT7sVWk9nwDz9KGS5o5Szs7QCAIeuTIn52hECKFeEPPwEl1Zu3MpiSAaoWPySBiQr4_PpGoLmckqK1VT4W2hjWx7PNOZ0dJqixeb5S3erGdY1gpPZScrV8YrfdSVxWWN56bvCtNkfefETY5fh8Nk15QKJ8Z1yq60-EV2pa47e40ucllZffMbx-jtab6dLr3VevE8TVZeCn5IvFhCRqn7NIhz5mc6DaNUKw00jwkAA8aBcz_2A8ZVzDmPopxrFWaKqJAyn9ExmpzmtqZ5P2jbiV1zMLVbKcCNiMD3gTjVw0mVmcZao3PRmnIvTS-AiAG0-ANaDKDFD2gxgHZufnKn-92_jN83XolA</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Zivanovic Radnic, T.</creator><creator>Simic-Pasalic, K.</creator><creator>Sefik-Bukilica, M.</creator><creator>Misirlic Dencic, S.</creator><creator>Stojkovic, T.</creator><creator>Damjanov, N.</creator><creator>Vojinovic, J.</creator><general>Elsevier Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>201506</creationdate><title>AB0510 Alphacalcidol Therapy Decreases GSH, SOD and Catalase Levels in Erythrocytes of Rheumatoid Arthritis Patients</title><author>Zivanovic Radnic, T. ; 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Vitamin D deficiency enhances oxidative stress that plays a substantial role in pathogenesis of autoimmune diseases.ObjectivesBecause erythrocytes are extremly vulnerabile to oxidative stress, the aim of this research was to analyse the effect of twelve weeks long alphacalcidol therapy in patients with RA on erythrocytes' glutathione (GSH), superoxide dismutase (SOD) and catalase levels, as an oxidative stress markers.MethodsIn ten patients with active RA (DAS28(SE) score >3.2) of both sexes, age 53.78±12.01 alphacalcidol (2μg/day) was added to previously applied therapy (stable dose of methotrexate, without any steroid therapy) during three months. Blood samples were taken before and after 12 weeks of alphacalcidol therapy. GSH, SOD and catalase levels in isolated and lysed erythrocytes were determined mannualy, using spectrophotometry method. Hemoglobin (Hb) levels were measured in lysed erythrocytes using biochemical analyser (Beckman coulter AcT diff) and levels expressed as μmol/g Hb for GSH and U/g Hb for catalase and SOD. In addition, parameters of inflammation (serum C-reactive protein (CRP) and sedimentation rate (SE)) were determined and disease activity was assessed using DAS28 (SE) score. Laboratory safety assessment of the study drug was evaluated monthly. Student's t-test was used for statistical analysis.ResultsAverage erythrocytes GSH level before treatment was 6.0±2.3 μmol/g Hb and it decreased to 3.7±1.3 μmol/g Hb (p=0.02) after treatment. Futhermore, initial catalase levels of 1412.3±840.2 U/ g Hb dropped to 211.3±119.1 U/g Hb (p=0.01) after twelve weeks of alphacalcidol therapy. Although slight reduction in SOD levels was observed after therapy, it was statistically insignificant. Significant clinical impovement was observed, DAS28(SE) was before treatment 5.81±0.89 and decreased to 4.31±1.03 (p=0.001), and CRP level of 28.41±28.16 dropped to 10.03±11.68 (p=0.000).ConclusionsDecreased levels of erythrocytes' GSH and catalase in RA patients after 12 weeks of alphacalcidol therapy indicate that alphacalcidol induced antioxidative effect. We assume that alphacalcidol lead to reduction of H2O2 production in erythrocytes and therefore decreased the need for antioxidative enzymes catalase and glutathione peroxidase activity. Antioxidative effect of alphacalcidol was in line with good clinical outcome in patients.Disclosure of InterestNone declared</abstract><cop>Kidlington</cop><pub>Elsevier Limited</pub><doi>10.1136/annrheumdis-2015-eular.3365</doi></addata></record> |
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