2012
DOI: 10.1016/j.sleep.2011.10.030
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Oxidative stress biomarkers in patients with untreated obstructive sleep apnea syndrome

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Cited by 69 publications
(47 citation statements)
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“…Other studies found that the severity of OSA was negatively correlated with total antioxidant capacity (TAC) [15] and positively correlated with urinary 8-hydroxy-2-deoxyguanosine (8-OHdG) excretion [16]. Oxidative stress markers such as TAC (defined as ferric reducing antioxidant power) were found to be useful in detecting and monitoring redox imbalance and the CPAP therapy effect in OSA patients without stroke [15]. The 8-OHdG is a modified deoxyribonucleic acid (DNA) base that has been used for evaluation of oxidative DNA damage [17].…”
Section: Introductionmentioning
confidence: 99%
“…Other studies found that the severity of OSA was negatively correlated with total antioxidant capacity (TAC) [15] and positively correlated with urinary 8-hydroxy-2-deoxyguanosine (8-OHdG) excretion [16]. Oxidative stress markers such as TAC (defined as ferric reducing antioxidant power) were found to be useful in detecting and monitoring redox imbalance and the CPAP therapy effect in OSA patients without stroke [15]. The 8-OHdG is a modified deoxyribonucleic acid (DNA) base that has been used for evaluation of oxidative DNA damage [17].…”
Section: Introductionmentioning
confidence: 99%
“…Most studies have found an elevated blood 8-isoprostane level in OSA subjects compared to non-OSA controls [39,40], and a randomized controlled study showed that levels were subsequently decreased after CPAP therapy for 3 months [41]. Similarly, AOPP levels were higher in untreated OSA subjects [17]. We found that elevated levels of 8-isoprostane correlated with OSA severity independent of age and BMI, and that AOPP also showed a similar correlation, but that the association became non-significant on adjustment for age and BMI.…”
Section: Discussionmentioning
confidence: 99%
“…Monocyte chemo-attractant protein-1 (MCP-1), a relatively novel biomarker mediating monocyte infiltration in atherosclerotic plaque, was found to be overly expressed in patients with severe OSA in a recent study [16]. Advanced oxidation protein products (AOPP) and 8-isoprostane, both biomarkers of oxidative stress, are being increasingly explored in various cardiometabolic disorders, including OSA [17,18]. …”
Section: Introductionmentioning
confidence: 99%
“…The continued hypoxia-reoxygenation episodes have a pivotal role in the pathogenesis of the endothelial dysfunction in OSAS: the intermittent hypoxia may induce the production of reactive oxygen species (ROS) that contribute to the generation of adhesion molecules, leukocyte activation, and an enhanced systemic inflammation leading to endothelial damage [21]. In OSAS an increase in lipid and protein oxidation [3,7,9,13,18,26] and a decrease in antioxidant defenses [7,9,16,23,27,30] have been demonstrated. In OSAS subjects the hypoxia-reoxygenation phenomena influence nitric oxide (NO) synthesis by NO synthase (NOS) inducing a down-regulation of the eNOs expression [32,33] and activation [15] and a simultaneous increase in inducible NOS (iNOS) expression [15].…”
Section: Introductionmentioning
confidence: 99%