2013
DOI: 10.1111/1756-185x.12140
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Antioxidant profile in patients with complex regional pain syndrome type I

Abstract: Our findings suggest a possible role of oxidative stress in the pathogenesis of CRPS.

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Cited by 13 publications
(11 citation statements)
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“…Abnormalities in plasma levels of various amino acids 48 , antioxidants 49 and circulating CD14 + CD16 + monocytes 50 have also been described in CRPS, but unfortunately in studies that did not include appropriate pain control groups. Therefore, the utility of these factors as biomarkers for CRPS remains to be determined.…”
Section: Diagnostic Features and Biomarkersmentioning
confidence: 99%
“…Abnormalities in plasma levels of various amino acids 48 , antioxidants 49 and circulating CD14 + CD16 + monocytes 50 have also been described in CRPS, but unfortunately in studies that did not include appropriate pain control groups. Therefore, the utility of these factors as biomarkers for CRPS remains to be determined.…”
Section: Diagnostic Features and Biomarkersmentioning
confidence: 99%
“…Furthermore, under normal conditions, the antioxidant defense system neutralizes excess free radicals to prevent damage [42][43][44]. While oxidative stress has been associated to painful conditions [26,[45][46][47][48], the direct link is not yet understood. It is hypothesized that oxidative stress contributes to pain by exacerbating pathological responses like inflammation and neuropathy, which both contribute to pain.…”
Section: Oxidative Stress and Painmentioning
confidence: 99%
“…Several lines of evidence from human studies suggest oxidative stress in the limbs of patients with CRPS. [61][62][63] Nociceptive sensitization and elevated markers of oxidative stress have been noted in the limbs of laboratory animals used with either the ischemia-reperfusion or the tibial fracture model of CRPS, changes that can be reduced by the administration of antioxidant drugs like N-acetyl cysteine and vitamin C. 50,64 Using the tibial fracture model, it was observed that oxidative stress caused the upregulation of SP and CGRP that in turn were critical for the production of inflammatory cytokines (IL-6) and the pain-related neurotrophin NGF. 50 While the most extensive data regarding inflammation and cytokine production in CRPS pertain to skin, muscle, and joints, elevations in cytokine production in spinal cord tissue have been noted as well after fracture and cast immobilization.…”
Section: Autoinflammation and Crps (Cytokine Production)mentioning
confidence: 99%