2012
DOI: 10.1111/j.1447-0756.2011.01771.x
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Role of oxidative stress in preeclampsia and intrauterine growth restriction

Abstract: Increased oxidative stress and antioxidative defense mechanisms may contribute to disease processes both in preeclampsia and IUGR.

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Cited by 109 publications
(82 citation statements)
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References 40 publications
(62 reference statements)
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“…The PE group, however, showed no statistically significant difference from control (Wiktor et al 2004). Other studies on the same subject showed similar conclusions, with oxidative stress levels being higher in the groups that exhibit both pathologies (Fujimaki et al 2011;Mert et al 2012). These findings suggest a correlation be-tween the severity of the deficiency in the interaction between cytotrophoblasts and the maternal spiral arteries, both representative of IUGR and PE, and the levels of oxidative stress (Wiktor et al 2004).…”
Section: Intrauterine Growth Restrictionsupporting
confidence: 71%
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“…The PE group, however, showed no statistically significant difference from control (Wiktor et al 2004). Other studies on the same subject showed similar conclusions, with oxidative stress levels being higher in the groups that exhibit both pathologies (Fujimaki et al 2011;Mert et al 2012). These findings suggest a correlation be-tween the severity of the deficiency in the interaction between cytotrophoblasts and the maternal spiral arteries, both representative of IUGR and PE, and the levels of oxidative stress (Wiktor et al 2004).…”
Section: Intrauterine Growth Restrictionsupporting
confidence: 71%
“…Despite having distinctive clinical manifestations, there is accumulating evidence that the two pathologies have a common cause: an abnormal placental implantation (Mert et al 2012). Several studies have been conducted in order to understand if the two pathologies are related (Fujimaki et al 2011;Mert et al 2012;Takagi et al 2004;Wiktor et al 2004).…”
Section: Intrauterine Growth Restrictionmentioning
confidence: 99%
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“…However, previous studies reported conflicting results of maternal serum PON and arylesterase levels in preeclampsia [15,21]. Furthermore, the reported total oxidant status (TOS), total antioxidant status (TAS), and oxidative stress index (OSI) values were also controversial in different studies [10,22]. Considering the results of the above-mentioned studies, we hypothesized that since preeclampsia and atherosclerotic diseases share a common pathophysiological mechanism, namely endothelial dysfunction, it may cause alterations in the perfusion of the utero-placental-fetal unit and lead to adverse perinatal outcomes.…”
Section: Introductionmentioning
confidence: 89%
“…Endothelial dysfunction results in increased systemic vascular resistance, leading to reduced perfusion in maternal systems, including the placenta [9]. Reduced perfusion aggravates placental ischemia-reperfusion injury, which is a strong stimulus for the production of reactive oxygen species (ROS) [10]. Additionally, increased generation of ROS, increased lipid peroxidation, and/or decreased antioxidant status further exacerbate endothelial dysfunction [11].…”
Section: Introductionmentioning
confidence: 99%