Study of oxidative stress in patients with advanced renal disease and undergoing either hemodialysis or peritoneal dialysis
Oxidative stress (OS) is directly involved in the formation of atheroma plaque and has been shown to be present since the early stages of Chronic Kidney Disease (CKD); however, the net role that dialytica techniques may play in OS process is yet to be determined. We studied three groups: hemodialysi...
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Veröffentlicht in: | Clinical nephrology 2013-09, Vol.80 (3), p.177-186 |
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creator | Puchades, Maria J Saez, Guillermo Muñoz, M Carmen Gonzalez, Miguel Torregrosa, Isidro Juan, Isabel Miguel, Alfonso |
description | Oxidative stress (OS) is directly involved in the formation of atheroma plaque and has been shown to be present since the early stages of Chronic Kidney Disease (CKD); however, the net role that dialytica techniques may play in OS process is yet to be determined. We studied three groups: hemodialysis (HD, n = 30), peritoneal dialysis (PD, n = 31), predialysis (pre-D, n = 32), and one control group (C, n = 67). Using highresolution liquid chromatography columns (HPLC), the superoxide dismutase (SOD), glutathione oxidized/reduced ratio (GSSG/GSH), and nuclear, as well as mitochondrial 8-oxo-dG (8-oxo-dG mit) were measured in lymphocytes. Protein carbonyls and F2-isoprostanes were measured in plasma. The antioxidant enzyme activity was evaluated by a spectrophotometric assay of catalase, glutathione peroxidase (GPX), glutathione reductase (GSR), and superoxide dismutase (SOD). Compared to the control group, all groups had significantly higher levels of products derived from molecular oxidation with a significant decrease in antioxidant enzymes. Patients in the pre-D group showed higher values for most of the oxidized molecules. The PD group showed a better oxidative balance, with no significant differences in levels of mitochondrial 8-oxo-dG when compared to the control group. We speculated that the better control of OS observed in patients receiving PD might be explained by the fact that this technique is more biocompatible, and this might help reduce the risk of cardiovascular events. |
doi_str_mv | 10.5414/CN107639 |
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We studied three groups: hemodialysis (HD, n = 30), peritoneal dialysis (PD, n = 31), predialysis (pre-D, n = 32), and one control group (C, n = 67). Using highresolution liquid chromatography columns (HPLC), the superoxide dismutase (SOD), glutathione oxidized/reduced ratio (GSSG/GSH), and nuclear, as well as mitochondrial 8-oxo-dG (8-oxo-dG mit) were measured in lymphocytes. Protein carbonyls and F2-isoprostanes were measured in plasma. The antioxidant enzyme activity was evaluated by a spectrophotometric assay of catalase, glutathione peroxidase (GPX), glutathione reductase (GSR), and superoxide dismutase (SOD). Compared to the control group, all groups had significantly higher levels of products derived from molecular oxidation with a significant decrease in antioxidant enzymes. Patients in the pre-D group showed higher values for most of the oxidized molecules. The PD group showed a better oxidative balance, with no significant differences in levels of mitochondrial 8-oxo-dG when compared to the control group. We speculated that the better control of OS observed in patients receiving PD might be explained by the fact that this technique is more biocompatible, and this might help reduce the risk of cardiovascular events.</description><identifier>ISSN: 0301-0430</identifier><identifier>DOI: 10.5414/CN107639</identifier><identifier>PMID: 23782545</identifier><language>eng</language><publisher>Germany</publisher><subject>Adult ; Aged ; Biomarkers - blood ; Case-Control Studies ; Catalase - blood ; Chi-Square Distribution ; Chromatography, High Pressure Liquid ; Cross-Sectional Studies ; Deoxyguanosine - analogs & derivatives ; Deoxyguanosine - blood ; DNA Damage ; F2-Isoprostanes - blood ; Female ; Glutathione - blood ; Glutathione Peroxidase - blood ; Glutathione Reductase - blood ; Humans ; Kidney Diseases - blood ; Kidney Diseases - therapy ; Linear Models ; Lipid Peroxidation ; Male ; Middle Aged ; Multivariate Analysis ; Oxidative Stress ; Peritoneal Dialysis ; Protein Carbonylation ; Renal Dialysis ; Superoxide Dismutase - blood ; Treatment Outcome ; Up-Regulation</subject><ispartof>Clinical nephrology, 2013-09, Vol.80 (3), p.177-186</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c283t-5a905ccda4a61e5215927f713f6f726fa975e2502d50ca9591509f9d63ec29a43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23782545$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Puchades, Maria J</creatorcontrib><creatorcontrib>Saez, Guillermo</creatorcontrib><creatorcontrib>Muñoz, M Carmen</creatorcontrib><creatorcontrib>Gonzalez, Miguel</creatorcontrib><creatorcontrib>Torregrosa, Isidro</creatorcontrib><creatorcontrib>Juan, Isabel</creatorcontrib><creatorcontrib>Miguel, Alfonso</creatorcontrib><title>Study of oxidative stress in patients with advanced renal disease and undergoing either hemodialysis or peritoneal dialysis</title><title>Clinical nephrology</title><addtitle>Clin Nephrol</addtitle><description>Oxidative stress (OS) is directly involved in the formation of atheroma plaque and has been shown to be present since the early stages of Chronic Kidney Disease (CKD); however, the net role that dialytica techniques may play in OS process is yet to be determined. We studied three groups: hemodialysis (HD, n = 30), peritoneal dialysis (PD, n = 31), predialysis (pre-D, n = 32), and one control group (C, n = 67). Using highresolution liquid chromatography columns (HPLC), the superoxide dismutase (SOD), glutathione oxidized/reduced ratio (GSSG/GSH), and nuclear, as well as mitochondrial 8-oxo-dG (8-oxo-dG mit) were measured in lymphocytes. Protein carbonyls and F2-isoprostanes were measured in plasma. The antioxidant enzyme activity was evaluated by a spectrophotometric assay of catalase, glutathione peroxidase (GPX), glutathione reductase (GSR), and superoxide dismutase (SOD). Compared to the control group, all groups had significantly higher levels of products derived from molecular oxidation with a significant decrease in antioxidant enzymes. Patients in the pre-D group showed higher values for most of the oxidized molecules. The PD group showed a better oxidative balance, with no significant differences in levels of mitochondrial 8-oxo-dG when compared to the control group. We speculated that the better control of OS observed in patients receiving PD might be explained by the fact that this technique is more biocompatible, and this might help reduce the risk of cardiovascular events.</description><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers - blood</subject><subject>Case-Control Studies</subject><subject>Catalase - blood</subject><subject>Chi-Square Distribution</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Cross-Sectional Studies</subject><subject>Deoxyguanosine - analogs & derivatives</subject><subject>Deoxyguanosine - blood</subject><subject>DNA Damage</subject><subject>F2-Isoprostanes - blood</subject><subject>Female</subject><subject>Glutathione - blood</subject><subject>Glutathione Peroxidase - blood</subject><subject>Glutathione Reductase - blood</subject><subject>Humans</subject><subject>Kidney Diseases - blood</subject><subject>Kidney Diseases - therapy</subject><subject>Linear Models</subject><subject>Lipid Peroxidation</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Oxidative Stress</subject><subject>Peritoneal Dialysis</subject><subject>Protein Carbonylation</subject><subject>Renal Dialysis</subject><subject>Superoxide Dismutase - blood</subject><subject>Treatment Outcome</subject><subject>Up-Regulation</subject><issn>0301-0430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkDtPwzAURj2AaClI_ALkkSXgR5zEI6p4SRUMwBwZ-6Y1SuxgO4WKP0-gFKYrfTr3DAehE0rORU7zi_k9JWXB5R6aEk5oRnJOJugwxldCGKl4dYAmjJcVE7mYos_HNJgN9g32H9aoZNeAYwoQI7YO9-MALkX8btMKK7NWToPBAZxqsbERVASsnMGDMxCW3rolhhGFgFfQeWNVu4k2Yh9wD8Em7-DncTsfof1GtRGOf-8MPV9fPc1vs8XDzd38cpFpVvGUCSWJ0NqoXBUUBKNCsrIpKW-KpmRFo2QpgAnCjCBaSSGpILKRpuCgmVQ5n6GzrbcP_m2AmOrORg1tqxz4IdY0Z3K0FkL8ozr4GAM0dR9sp8KmpqT-zlvv8o7o6a91eOnA_IG7tvwL4T94rg</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Puchades, Maria J</creator><creator>Saez, Guillermo</creator><creator>Muñoz, M Carmen</creator><creator>Gonzalez, Miguel</creator><creator>Torregrosa, Isidro</creator><creator>Juan, Isabel</creator><creator>Miguel, Alfonso</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130901</creationdate><title>Study of oxidative stress in patients with advanced renal disease and undergoing either hemodialysis or peritoneal dialysis</title><author>Puchades, Maria J ; Saez, Guillermo ; Muñoz, M Carmen ; Gonzalez, Miguel ; Torregrosa, Isidro ; Juan, Isabel ; Miguel, Alfonso</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c283t-5a905ccda4a61e5215927f713f6f726fa975e2502d50ca9591509f9d63ec29a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers - blood</topic><topic>Case-Control Studies</topic><topic>Catalase - blood</topic><topic>Chi-Square Distribution</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Cross-Sectional Studies</topic><topic>Deoxyguanosine - analogs & derivatives</topic><topic>Deoxyguanosine - blood</topic><topic>DNA Damage</topic><topic>F2-Isoprostanes - blood</topic><topic>Female</topic><topic>Glutathione - blood</topic><topic>Glutathione Peroxidase - blood</topic><topic>Glutathione Reductase - blood</topic><topic>Humans</topic><topic>Kidney Diseases - blood</topic><topic>Kidney Diseases - therapy</topic><topic>Linear Models</topic><topic>Lipid Peroxidation</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Oxidative Stress</topic><topic>Peritoneal Dialysis</topic><topic>Protein Carbonylation</topic><topic>Renal Dialysis</topic><topic>Superoxide Dismutase - blood</topic><topic>Treatment Outcome</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Puchades, Maria J</creatorcontrib><creatorcontrib>Saez, Guillermo</creatorcontrib><creatorcontrib>Muñoz, M Carmen</creatorcontrib><creatorcontrib>Gonzalez, Miguel</creatorcontrib><creatorcontrib>Torregrosa, Isidro</creatorcontrib><creatorcontrib>Juan, Isabel</creatorcontrib><creatorcontrib>Miguel, Alfonso</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Puchades, Maria J</au><au>Saez, Guillermo</au><au>Muñoz, M Carmen</au><au>Gonzalez, Miguel</au><au>Torregrosa, Isidro</au><au>Juan, Isabel</au><au>Miguel, Alfonso</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of oxidative stress in patients with advanced renal disease and undergoing either hemodialysis or peritoneal dialysis</atitle><jtitle>Clinical nephrology</jtitle><addtitle>Clin Nephrol</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>80</volume><issue>3</issue><spage>177</spage><epage>186</epage><pages>177-186</pages><issn>0301-0430</issn><abstract>Oxidative stress (OS) is directly involved in the formation of atheroma plaque and has been shown to be present since the early stages of Chronic Kidney Disease (CKD); however, the net role that dialytica techniques may play in OS process is yet to be determined. We studied three groups: hemodialysis (HD, n = 30), peritoneal dialysis (PD, n = 31), predialysis (pre-D, n = 32), and one control group (C, n = 67). Using highresolution liquid chromatography columns (HPLC), the superoxide dismutase (SOD), glutathione oxidized/reduced ratio (GSSG/GSH), and nuclear, as well as mitochondrial 8-oxo-dG (8-oxo-dG mit) were measured in lymphocytes. Protein carbonyls and F2-isoprostanes were measured in plasma. The antioxidant enzyme activity was evaluated by a spectrophotometric assay of catalase, glutathione peroxidase (GPX), glutathione reductase (GSR), and superoxide dismutase (SOD). Compared to the control group, all groups had significantly higher levels of products derived from molecular oxidation with a significant decrease in antioxidant enzymes. Patients in the pre-D group showed higher values for most of the oxidized molecules. The PD group showed a better oxidative balance, with no significant differences in levels of mitochondrial 8-oxo-dG when compared to the control group. We speculated that the better control of OS observed in patients receiving PD might be explained by the fact that this technique is more biocompatible, and this might help reduce the risk of cardiovascular events.</abstract><cop>Germany</cop><pmid>23782545</pmid><doi>10.5414/CN107639</doi><tpages>10</tpages></addata></record> |
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subjects | Adult Aged Biomarkers - blood Case-Control Studies Catalase - blood Chi-Square Distribution Chromatography, High Pressure Liquid Cross-Sectional Studies Deoxyguanosine - analogs & derivatives Deoxyguanosine - blood DNA Damage F2-Isoprostanes - blood Female Glutathione - blood Glutathione Peroxidase - blood Glutathione Reductase - blood Humans Kidney Diseases - blood Kidney Diseases - therapy Linear Models Lipid Peroxidation Male Middle Aged Multivariate Analysis Oxidative Stress Peritoneal Dialysis Protein Carbonylation Renal Dialysis Superoxide Dismutase - blood Treatment Outcome Up-Regulation |
title | Study of oxidative stress in patients with advanced renal disease and undergoing either hemodialysis or peritoneal dialysis |
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