F. Avilés-Plaza, J. Bernabé, Begoña Cerdá, Javier Marhuenda, P. Zafrilla, Tânia Constantino, J. Mulero, C. García-Viguera, D. Moreno, J. Abellán, S. Parra-Pallarés
{"title":"代谢综合征患者氧化应激的生物标志物,一项病例对照研究","authors":"F. Avilés-Plaza, J. Bernabé, Begoña Cerdá, Javier Marhuenda, P. Zafrilla, Tânia Constantino, J. Mulero, C. García-Viguera, D. Moreno, J. Abellán, S. Parra-Pallarés","doi":"10.4172/2167-0943.1000187","DOIUrl":null,"url":null,"abstract":"Abstract \nBackground: Owing to the proposal of the increase of oxidative stress (OxS) as an early event in the development of the metabolic syndrome (MetS), the aim of the present study was to evaluate certain OxS biomarkers in patients with MetS compared to healthy people age-matched and younger to assess the relevance of aging in OxS and MetS. \nMethods: A total of 72 patients, 32 who fulfilled the Adult Treatment Panel III criteria for the MetS and 40 individuals without MetS, 20 age-matched to the MetS patients (Control I) and 20 younger subjects (Control II) were studied. We measured several anthropometric and serum parameters and two kinds of molecules related to OxS: modified molecules by reactive oxygen species (ROS) such as oxidized LDL (oxLDLc), and consumed or inducted molecules (enzymes or antioxidants such as Glutathione reductase GR,) associated with ROS metabolism. The statistical analysis was performed using SPSS v18.0. \nResults: Only significant differences were observed in the values of GR between the MetS patients and Control I (50.31 ± 8.15 U/L vs 59.50 ± 9.98 U/L). We found significantly higher levels in the MetS patients compared to Control II of oxLDLc (96.77 ± 23.05 U/L vs 60.17 ± 16.28 U/L), F2 -isoprostanes (3.17 ± 1.78 µg/g creatinine vs 2.04 ± 0.80 µg/g creatinine) and protein cabonils (PC) (0.56 ± 0.26 nmol/mg vs 0.29 ± 0.13 nmol/mg). \nConclusions: Results have shown that MetS patients don’t present a superior OxS in comparison to age-related healthy individuals. Finally, aging is more relevant to OxS than MetS per se.","PeriodicalId":16452,"journal":{"name":"Journal of metabolic syndrome","volume":"36 1","pages":"1-5"},"PeriodicalIF":0.0000,"publicationDate":"2015-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Biomarkers of Oxidative Stress in Syndrome Metabolic Patients, a CaseControl Study\",\"authors\":\"F. Avilés-Plaza, J. Bernabé, Begoña Cerdá, Javier Marhuenda, P. Zafrilla, Tânia Constantino, J. Mulero, C. García-Viguera, D. Moreno, J. Abellán, S. 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The statistical analysis was performed using SPSS v18.0. \\nResults: Only significant differences were observed in the values of GR between the MetS patients and Control I (50.31 ± 8.15 U/L vs 59.50 ± 9.98 U/L). We found significantly higher levels in the MetS patients compared to Control II of oxLDLc (96.77 ± 23.05 U/L vs 60.17 ± 16.28 U/L), F2 -isoprostanes (3.17 ± 1.78 µg/g creatinine vs 2.04 ± 0.80 µg/g creatinine) and protein cabonils (PC) (0.56 ± 0.26 nmol/mg vs 0.29 ± 0.13 nmol/mg). \\nConclusions: Results have shown that MetS patients don’t present a superior OxS in comparison to age-related healthy individuals. 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引用次数: 1
摘要
背景:由于氧化应激(OxS)的增加是代谢综合征(MetS)发展的早期事件,本研究的目的是将代谢综合征患者的某些OxS生物标志物与年龄匹配和更年轻的健康人进行比较,以评估衰老在OxS和MetS中的相关性。方法:共研究了72例患者,其中32例符合MetS成人治疗组III标准,40例无MetS, 20例年龄与MetS患者相匹配(对照I), 20例年轻受试者(对照II)。我们测量了几种人体测量和血清参数以及与OxS相关的两种分子:一种是被活性氧(ROS)修饰的分子,如氧化LDL (oxLDLc),另一种是被消耗或诱导的与ROS代谢相关的分子(酶或抗氧化剂,如谷胱甘肽还原酶GR)。采用SPSS v18.0进行统计分析。结果:met组与对照组间GR值仅有显著差异(50.31±8.15 U/L vs 59.50±9.98 U/L)。我们发现,与对照组II相比,MetS患者的oxLDLc(96.77±23.05 U/L vs 60.17±16.28 U/L), F2 -异前列腺素(3.17±1.78µg/g肌酐vs 2.04±0.80µg/g肌酐)和蛋白质cabonils (PC)(0.56±0.26 nmol/mg vs 0.29±0.13 nmol/mg)水平显著高于对照组II。结论:结果表明,与年龄相关的健康人相比,MetS患者的OxS并不优越。最后,与MetS本身相比,衰老与OxS的关系更大。
Biomarkers of Oxidative Stress in Syndrome Metabolic Patients, a CaseControl Study
Abstract
Background: Owing to the proposal of the increase of oxidative stress (OxS) as an early event in the development of the metabolic syndrome (MetS), the aim of the present study was to evaluate certain OxS biomarkers in patients with MetS compared to healthy people age-matched and younger to assess the relevance of aging in OxS and MetS.
Methods: A total of 72 patients, 32 who fulfilled the Adult Treatment Panel III criteria for the MetS and 40 individuals without MetS, 20 age-matched to the MetS patients (Control I) and 20 younger subjects (Control II) were studied. We measured several anthropometric and serum parameters and two kinds of molecules related to OxS: modified molecules by reactive oxygen species (ROS) such as oxidized LDL (oxLDLc), and consumed or inducted molecules (enzymes or antioxidants such as Glutathione reductase GR,) associated with ROS metabolism. The statistical analysis was performed using SPSS v18.0.
Results: Only significant differences were observed in the values of GR between the MetS patients and Control I (50.31 ± 8.15 U/L vs 59.50 ± 9.98 U/L). We found significantly higher levels in the MetS patients compared to Control II of oxLDLc (96.77 ± 23.05 U/L vs 60.17 ± 16.28 U/L), F2 -isoprostanes (3.17 ± 1.78 µg/g creatinine vs 2.04 ± 0.80 µg/g creatinine) and protein cabonils (PC) (0.56 ± 0.26 nmol/mg vs 0.29 ± 0.13 nmol/mg).
Conclusions: Results have shown that MetS patients don’t present a superior OxS in comparison to age-related healthy individuals. Finally, aging is more relevant to OxS than MetS per se.