AB0898 The Total Antioxidant Status and Oxidative Stress in Patients with Osteoporosis

BackgroundEvidences have linked aging and the development of age-related diseases to increased levels of oxidative stress (OS). Increased OS in bone enhances osteoblast and osteocyte apoptosis, leading to decrease osteoblast number, and in turn decrease in bone formation (1). Free radicals are toxic...

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description BackgroundEvidences have linked aging and the development of age-related diseases to increased levels of oxidative stress (OS). Increased OS in bone enhances osteoblast and osteocyte apoptosis, leading to decrease osteoblast number, and in turn decrease in bone formation (1). Free radicals are toxic to osteoblasts and may stimulate osteoclast differentiation (2). In addition osteoclasts themselves are activated by free-radicals and they in turn produce free-radicals to resorb bone (3). Free radicals activate nuclear factor κβ (NFκβ), a factor responsible for the synthesis of bone-resorbing cytokines such as interleukin-1 and interleukin-6 (4).ObjectivesTo assess the total antioxidant status (TAS) and oxidative stress in patients with osteoporosis (OP).MethodsSixty female with positive Dual-Energy X-Ray Absorptiometry (DEXA) results whose ages range between 50 - 60 years old were enrolled in the study and were divided into 2 groups, osteopenia and osteoporosis. Thirty apparently healthy females, age matched with the patients, were kept as a control. TAS and Malondyaldehyde (MDA) were measured in all groups. A pilot study was designed to compare the TAS and MDA between patients with osteopenia and osteoporosis, using the ranges of T-score between the medians of each group (-1.7 to -2.5 and -2.6 to -3.3, respectivly).ResultsThe TAS values of patients groups (1.59±0.15 mmol/l and 1.05±0.37 mmol/l, were significantly lower than that of the control group (2.18±0.26mmol/l) (p
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Increased OS in bone enhances osteoblast and osteocyte apoptosis, leading to decrease osteoblast number, and in turn decrease in bone formation (1). Free radicals are toxic to osteoblasts and may stimulate osteoclast differentiation (2). In addition osteoclasts themselves are activated by free-radicals and they in turn produce free-radicals to resorb bone (3). Free radicals activate nuclear factor κβ (NFκβ), a factor responsible for the synthesis of bone-resorbing cytokines such as interleukin-1 and interleukin-6 (4).ObjectivesTo assess the total antioxidant status (TAS) and oxidative stress in patients with osteoporosis (OP).MethodsSixty female with positive Dual-Energy X-Ray Absorptiometry (DEXA) results whose ages range between 50 - 60 years old were enrolled in the study and were divided into 2 groups, osteopenia and osteoporosis. Thirty apparently healthy females, age matched with the patients, were kept as a control. TAS and Malondyaldehyde (MDA) were measured in all groups. A pilot study was designed to compare the TAS and MDA between patients with osteopenia and osteoporosis, using the ranges of T-score between the medians of each group (-1.7 to -2.5 and -2.6 to -3.3, respectivly).ResultsThe TAS values of patients groups (1.59±0.15 mmol/l and 1.05±0.37 mmol/l, were significantly lower than that of the control group (2.18±0.26mmol/l) (p&lt;0.001). MDA values (1.20±0.43 μmol/l and 2.40±0.66 μmol/l, respectively), were significantly higher than that of the control group (0.47±0.14 μmol/l) (p&lt;0.001).The result of pilot study, showed no difference between these two selected values groups for TAS and MDA, (p-value &lt;0.1and 0.07) respectivlly.Table 1.The TAS and MDA among the studied groupsParametersControlOsteopeniaOsteoporosisTAS (mmol/l)2.18±0.261.59±0.151.05±0.37MDA (μmol/l)0.47±0.141.20±0.432.40±0.66Table 2.The result of pilot studyParametersOsteopeniaOsteoporosisP valueTAS (mmol/l)1.47±0.111.40±0.120.07MDA (μmol/l)1.60±0.201.71±0.240.1ConclusionsThe OP patients have lower levels of TAS and higher levels of MDA than the control group. There is no difference between osteopenia and osteoporosis regarding oxidative stress in the pilot study.ReferencesAlmeida M, Han L, Ambrogini E, Weinstein RS, Manolagas SC Glucocorticoids and tumor necrosis factor α increase oxidative stress and suppress Wnt protein signaling in osteoblasts. J Bone Miner Res 2011; 26(11):2682-94.Ahmad NS, Khalid BAK, Luke DA, Ima-Nirwana S. Tocotrienol offers better protection than tocopherol from free radical-induced damage of rat bone. Clin Exp Pharm Physiol 2005; 32: 761-770.Garrett I R et al., Oxygen-derived free radicals stimulate osteoclastic bone resorption in rodent bone in vitro and in vivo. J Clin Invest 1990; 85(3): 632-639.Basu S, Michaelsson K, Olofsson H, Johansson S &amp; Melhus H. Association between oxidative stress and bone mineral density. Biochem Biophys Res Commun 2001; 288:275-279.Disclosure of InterestNone declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2015-eular.1066</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.1200</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_2/1200.3.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/74/Suppl_2/1200.3.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3182,23551,27903,27904,77347,77378</link.rule.ids></links><search><creatorcontrib>Abdullah, K.S.</creatorcontrib><title>AB0898 The Total Antioxidant Status and Oxidative Stress in Patients with Osteoporosis</title><title>Annals of the rheumatic diseases</title><description>BackgroundEvidences have linked aging and the development of age-related diseases to increased levels of oxidative stress (OS). Increased OS in bone enhances osteoblast and osteocyte apoptosis, leading to decrease osteoblast number, and in turn decrease in bone formation (1). Free radicals are toxic to osteoblasts and may stimulate osteoclast differentiation (2). In addition osteoclasts themselves are activated by free-radicals and they in turn produce free-radicals to resorb bone (3). Free radicals activate nuclear factor κβ (NFκβ), a factor responsible for the synthesis of bone-resorbing cytokines such as interleukin-1 and interleukin-6 (4).ObjectivesTo assess the total antioxidant status (TAS) and oxidative stress in patients with osteoporosis (OP).MethodsSixty female with positive Dual-Energy X-Ray Absorptiometry (DEXA) results whose ages range between 50 - 60 years old were enrolled in the study and were divided into 2 groups, osteopenia and osteoporosis. Thirty apparently healthy females, age matched with the patients, were kept as a control. TAS and Malondyaldehyde (MDA) were measured in all groups. A pilot study was designed to compare the TAS and MDA between patients with osteopenia and osteoporosis, using the ranges of T-score between the medians of each group (-1.7 to -2.5 and -2.6 to -3.3, respectivly).ResultsThe TAS values of patients groups (1.59±0.15 mmol/l and 1.05±0.37 mmol/l, were significantly lower than that of the control group (2.18±0.26mmol/l) (p&lt;0.001). MDA values (1.20±0.43 μmol/l and 2.40±0.66 μmol/l, respectively), were significantly higher than that of the control group (0.47±0.14 μmol/l) (p&lt;0.001).The result of pilot study, showed no difference between these two selected values groups for TAS and MDA, (p-value &lt;0.1and 0.07) respectivlly.Table 1.The TAS and MDA among the studied groupsParametersControlOsteopeniaOsteoporosisTAS (mmol/l)2.18±0.261.59±0.151.05±0.37MDA (μmol/l)0.47±0.141.20±0.432.40±0.66Table 2.The result of pilot studyParametersOsteopeniaOsteoporosisP valueTAS (mmol/l)1.47±0.111.40±0.120.07MDA (μmol/l)1.60±0.201.71±0.240.1ConclusionsThe OP patients have lower levels of TAS and higher levels of MDA than the control group. There is no difference between osteopenia and osteoporosis regarding oxidative stress in the pilot study.ReferencesAlmeida M, Han L, Ambrogini E, Weinstein RS, Manolagas SC Glucocorticoids and tumor necrosis factor α increase oxidative stress and suppress Wnt protein signaling in osteoblasts. J Bone Miner Res 2011; 26(11):2682-94.Ahmad NS, Khalid BAK, Luke DA, Ima-Nirwana S. Tocotrienol offers better protection than tocopherol from free radical-induced damage of rat bone. Clin Exp Pharm Physiol 2005; 32: 761-770.Garrett I R et al., Oxygen-derived free radicals stimulate osteoclastic bone resorption in rodent bone in vitro and in vivo. J Clin Invest 1990; 85(3): 632-639.Basu S, Michaelsson K, Olofsson H, Johansson S &amp; Melhus H. Association between oxidative stress and bone mineral density. Biochem Biophys Res Commun 2001; 288:275-279.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>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqVkLtOwzAUhi0EEqXwDpY6p_g0jp2IqSBuUqUikYHNcmJHddXaxXa4bCy8KE-CQxlYmazz6f-Pjz6EJkCmADk7l9b6le63yoRsRqDIdL-RfgqEsQM0AsrKhBk5RCNCSJ7RivFjdBLCOo2khHKEnuaXpKzKr4_PeqVx7aLc4LmNxr0ZJW3Ej1HGPmBpFV4OKJoXnaDXIWBj8UMC2saAX01c4WWI2u2cd8GEU3TUyU3QZ7_vGNU31_XVXbZY3t5fzRdZAzNOM16xgqiiyVuuWiULpjhrQXKomqZjRaUa6Nq8KSjVBStBzzRtO1CqIgC84_kYTfZrd9499zpEsXa9t-lHASlTAqdAU-pin2rTbcHrTuy82Ur_LoCIwaT4Y1IMJsWPSTGYTG22bzfb9b-K33JrgIg</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Abdullah, K.S.</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>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>201506</creationdate><title>AB0898 The Total Antioxidant Status and Oxidative Stress in Patients with Osteoporosis</title><author>Abdullah, K.S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1274-79650d5b3c7dcda56d76c1a719bbf659db1fc3b544e5681e2e4cf1dd90117f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abdullah, K.S.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; 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Increased OS in bone enhances osteoblast and osteocyte apoptosis, leading to decrease osteoblast number, and in turn decrease in bone formation (1). Free radicals are toxic to osteoblasts and may stimulate osteoclast differentiation (2). In addition osteoclasts themselves are activated by free-radicals and they in turn produce free-radicals to resorb bone (3). Free radicals activate nuclear factor κβ (NFκβ), a factor responsible for the synthesis of bone-resorbing cytokines such as interleukin-1 and interleukin-6 (4).ObjectivesTo assess the total antioxidant status (TAS) and oxidative stress in patients with osteoporosis (OP).MethodsSixty female with positive Dual-Energy X-Ray Absorptiometry (DEXA) results whose ages range between 50 - 60 years old were enrolled in the study and were divided into 2 groups, osteopenia and osteoporosis. Thirty apparently healthy females, age matched with the patients, were kept as a control. TAS and Malondyaldehyde (MDA) were measured in all groups. A pilot study was designed to compare the TAS and MDA between patients with osteopenia and osteoporosis, using the ranges of T-score between the medians of each group (-1.7 to -2.5 and -2.6 to -3.3, respectivly).ResultsThe TAS values of patients groups (1.59±0.15 mmol/l and 1.05±0.37 mmol/l, were significantly lower than that of the control group (2.18±0.26mmol/l) (p&lt;0.001). MDA values (1.20±0.43 μmol/l and 2.40±0.66 μmol/l, respectively), were significantly higher than that of the control group (0.47±0.14 μmol/l) (p&lt;0.001).The result of pilot study, showed no difference between these two selected values groups for TAS and MDA, (p-value &lt;0.1and 0.07) respectivlly.Table 1.The TAS and MDA among the studied groupsParametersControlOsteopeniaOsteoporosisTAS (mmol/l)2.18±0.261.59±0.151.05±0.37MDA (μmol/l)0.47±0.141.20±0.432.40±0.66Table 2.The result of pilot studyParametersOsteopeniaOsteoporosisP valueTAS (mmol/l)1.47±0.111.40±0.120.07MDA (μmol/l)1.60±0.201.71±0.240.1ConclusionsThe OP patients have lower levels of TAS and higher levels of MDA than the control group. There is no difference between osteopenia and osteoporosis regarding oxidative stress in the pilot study.ReferencesAlmeida M, Han L, Ambrogini E, Weinstein RS, Manolagas SC Glucocorticoids and tumor necrosis factor α increase oxidative stress and suppress Wnt protein signaling in osteoblasts. J Bone Miner Res 2011; 26(11):2682-94.Ahmad NS, Khalid BAK, Luke DA, Ima-Nirwana S. Tocotrienol offers better protection than tocopherol from free radical-induced damage of rat bone. Clin Exp Pharm Physiol 2005; 32: 761-770.Garrett I R et al., Oxygen-derived free radicals stimulate osteoclastic bone resorption in rodent bone in vitro and in vivo. J Clin Invest 1990; 85(3): 632-639.Basu S, Michaelsson K, Olofsson H, Johansson S &amp; Melhus H. Association between oxidative stress and bone mineral density. Biochem Biophys Res Commun 2001; 288:275-279.Disclosure of InterestNone declared</abstract><cop>Kidlington</cop><pub>Elsevier Limited</pub><doi>10.1136/annrheumdis-2015-eular.1066</doi></addata></record>
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