Antioxidant profile in patients with complex regional pain syndrome type I

Objective Complex regional pain syndrome (CRPS) type I is one of the most important problems with regard to physical medicine and rehabilitation. CRPS may cause not only higher therapeutic costs but also greater work time loss. The mechanism and pathogenesis of CRPS still remains unknown. Some findi...

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Veröffentlicht in:International journal of rheumatic diseases 2014-02, Vol.17 (2), p.156-158
Hauptverfasser: Baykal, Tuba, Seferoglu, Buminhan, Karsan, Orhan, Kiziltunc, Ahmet, Senel, Kazim
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container_end_page 158
container_issue 2
container_start_page 156
container_title International journal of rheumatic diseases
container_volume 17
creator Baykal, Tuba
Seferoglu, Buminhan
Karsan, Orhan
Kiziltunc, Ahmet
Senel, Kazim
description Objective Complex regional pain syndrome (CRPS) type I is one of the most important problems with regard to physical medicine and rehabilitation. CRPS may cause not only higher therapeutic costs but also greater work time loss. The mechanism and pathogenesis of CRPS still remains unknown. Some findings indicating oxidative stress have been reported. This study was carried out to determine the role of oxidative stress in patients with CRPS. Materials and methods Twenty patients (13 women and seven men) with CRPS and 20 age‐ and sex‐matched healthy controls were enrolled in this study. Complex regional pain syndrome was diagnosed according to the modified International Association for the Study of Pain (IASP) criteria. We evaluated demographic, clinical and laboratory characteristics of the patients. Antioxidant enzymatic activities consisting of serum superoxide dismutase (SOD), glutathion peroxidase (GPX) and glutathione S‐transferase (GST) activities were measured using appropriate methods and compared with healthy controls. Results The mean age of the patients was 39.5 years and the mean duration of symptoms was 5.5 months. Complex regional pain syndrome devoleped after a traumatic event in 90% of patients. In 10% of patients there were no traumatic events. SOD, GPX and GST levels were significantly higher in patients with CRPS than healthy controls (P = 0.012, P = 0.036 and P = 0.016, respectively). Conclusion Our findings suggest a possible role of oxidative stress in the pathogenesis of CRPS.
doi_str_mv 10.1111/1756-185X.12140
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CRPS may cause not only higher therapeutic costs but also greater work time loss. The mechanism and pathogenesis of CRPS still remains unknown. Some findings indicating oxidative stress have been reported. This study was carried out to determine the role of oxidative stress in patients with CRPS. Materials and methods Twenty patients (13 women and seven men) with CRPS and 20 age‐ and sex‐matched healthy controls were enrolled in this study. Complex regional pain syndrome was diagnosed according to the modified International Association for the Study of Pain (IASP) criteria. We evaluated demographic, clinical and laboratory characteristics of the patients. Antioxidant enzymatic activities consisting of serum superoxide dismutase (SOD), glutathion peroxidase (GPX) and glutathione S‐transferase (GST) activities were measured using appropriate methods and compared with healthy controls. Results The mean age of the patients was 39.5 years and the mean duration of symptoms was 5.5 months. Complex regional pain syndrome devoleped after a traumatic event in 90% of patients. In 10% of patients there were no traumatic events. SOD, GPX and GST levels were significantly higher in patients with CRPS than healthy controls (P = 0.012, P = 0.036 and P = 0.016, respectively). Conclusion Our findings suggest a possible role of oxidative stress in the pathogenesis of CRPS.</description><identifier>ISSN: 1756-1841</identifier><identifier>EISSN: 1756-185X</identifier><identifier>DOI: 10.1111/1756-185X.12140</identifier><identifier>PMID: 24576270</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; Antioxidants - analysis ; Biomarkers - blood ; Case-Control Studies ; Female ; Glutathione Peroxidase - blood ; Glutathione Transferase - blood ; Humans ; Male ; Middle Aged ; Oxidative Stress ; Pain Measurement ; Reflex Sympathetic Dystrophy - blood ; Reflex Sympathetic Dystrophy - diagnosis ; regional pain syndromes ; soft tissue rheumatism ; Superoxide Dismutase - blood ; Time Factors</subject><ispartof>International journal of rheumatic diseases, 2014-02, Vol.17 (2), p.156-158</ispartof><rights>2013 Asia Pacific League of Associations for Rheumatology and Wiley Publishing Asia Pty Ltd</rights><rights>2013 Asia Pacific League of Associations for Rheumatology and Wiley Publishing Asia Pty Ltd.</rights><rights>International Journal of Rheumatic Diseases © 2014 Asia Pacific League of Associations for Rheumatology and Wiley Publishing Asia Pty Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4350-c03174225efafdf7ddee3e6e74ce46f31866773be20a3dd4dbe22d6443eb13403</citedby><cites>FETCH-LOGICAL-c4350-c03174225efafdf7ddee3e6e74ce46f31866773be20a3dd4dbe22d6443eb13403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1756-185X.12140$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1756-185X.12140$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24576270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baykal, Tuba</creatorcontrib><creatorcontrib>Seferoglu, Buminhan</creatorcontrib><creatorcontrib>Karsan, Orhan</creatorcontrib><creatorcontrib>Kiziltunc, Ahmet</creatorcontrib><creatorcontrib>Senel, Kazim</creatorcontrib><title>Antioxidant profile in patients with complex regional pain syndrome type I</title><title>International journal of rheumatic diseases</title><addtitle>Int J Rheum Dis</addtitle><description>Objective Complex regional pain syndrome (CRPS) type I is one of the most important problems with regard to physical medicine and rehabilitation. CRPS may cause not only higher therapeutic costs but also greater work time loss. The mechanism and pathogenesis of CRPS still remains unknown. Some findings indicating oxidative stress have been reported. This study was carried out to determine the role of oxidative stress in patients with CRPS. Materials and methods Twenty patients (13 women and seven men) with CRPS and 20 age‐ and sex‐matched healthy controls were enrolled in this study. Complex regional pain syndrome was diagnosed according to the modified International Association for the Study of Pain (IASP) criteria. We evaluated demographic, clinical and laboratory characteristics of the patients. Antioxidant enzymatic activities consisting of serum superoxide dismutase (SOD), glutathion peroxidase (GPX) and glutathione S‐transferase (GST) activities were measured using appropriate methods and compared with healthy controls. Results The mean age of the patients was 39.5 years and the mean duration of symptoms was 5.5 months. Complex regional pain syndrome devoleped after a traumatic event in 90% of patients. In 10% of patients there were no traumatic events. SOD, GPX and GST levels were significantly higher in patients with CRPS than healthy controls (P = 0.012, P = 0.036 and P = 0.016, respectively). 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CRPS may cause not only higher therapeutic costs but also greater work time loss. The mechanism and pathogenesis of CRPS still remains unknown. Some findings indicating oxidative stress have been reported. This study was carried out to determine the role of oxidative stress in patients with CRPS. Materials and methods Twenty patients (13 women and seven men) with CRPS and 20 age‐ and sex‐matched healthy controls were enrolled in this study. Complex regional pain syndrome was diagnosed according to the modified International Association for the Study of Pain (IASP) criteria. We evaluated demographic, clinical and laboratory characteristics of the patients. Antioxidant enzymatic activities consisting of serum superoxide dismutase (SOD), glutathion peroxidase (GPX) and glutathione S‐transferase (GST) activities were measured using appropriate methods and compared with healthy controls. Results The mean age of the patients was 39.5 years and the mean duration of symptoms was 5.5 months. Complex regional pain syndrome devoleped after a traumatic event in 90% of patients. In 10% of patients there were no traumatic events. SOD, GPX and GST levels were significantly higher in patients with CRPS than healthy controls (P = 0.012, P = 0.036 and P = 0.016, respectively). Conclusion Our findings suggest a possible role of oxidative stress in the pathogenesis of CRPS.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24576270</pmid><doi>10.1111/1756-185X.12140</doi><tpages>3</tpages></addata></record>
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subjects Adult
Antioxidants - analysis
Biomarkers - blood
Case-Control Studies
Female
Glutathione Peroxidase - blood
Glutathione Transferase - blood
Humans
Male
Middle Aged
Oxidative Stress
Pain Measurement
Reflex Sympathetic Dystrophy - blood
Reflex Sympathetic Dystrophy - diagnosis
regional pain syndromes
soft tissue rheumatism
Superoxide Dismutase - blood
Time Factors
title Antioxidant profile in patients with complex regional pain syndrome type I
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