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Effect of Flavonoids on Oxidative Stress and Inflammation in Adults at Risk of Cardiovascular Disease: A Systematic Review

机译:黄酮类化合物对心血管疾病风险氧化应激和氧化应激和炎症的影响:系统评价

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Oxidative stress (OS) and inflammatory processes initiate the first stage of cardiovascular disease (CVD). Flavonoid consumption has been related to significantly improved flow-mediated dilation and blood pressure. Antioxidant and anti-inflammatory mechanisms are thought to be involved. The effect of flavonoids on markers of oxidative stress and inflammation, in at risk individuals is yet to be reviewed. Systematic literature searches were conducted in MEDLINE, Cochrane Library, CINAHL and SCOPUS databases. Randomised controlled trials in a Western country providing a food-based flavonoid intervention to participants with one or two modifiable risk factors for CVD measuring a marker of OS and/or inflammation, were included. Reference lists were hand-searched. The Cochrane Collaboration Risk of Bias Tool was used to assess study quality. The search strategy retrieved 1248 articles. Nineteen articles meeting the inclusion criteria were reviewed. Eight studies were considered at low risk of bias. Cocoa flavonoids provided to Type 2 diabetics and olive oil flavonoids to mildly-hypertensive women reduced OS and inflammation. Other food sources had weaker effects. No consistent effect on OS and inflammation across patients with varied CVD risk factors was observed. Study heterogeneity posed a challenge for inter-study comparisons. Rigorously designed studies will assist in determining the effectiveness of flavonoid interventions for reducing OS and inflammation in patients at risk of CVD.
机译:氧化应激(OS)和炎症过程引发心血管疾病(CVD)的第一阶段。黄酮类化合物消费与显着改善的流量介导的扩张和血压有关。认为抗氧化剂和抗炎机制涉及。黄酮类化合物对氧化应激和炎症标志物的影响尚未审查。系统文献搜索是在Medline,Cochrane图书馆,CINAHL和SCOPUS数据库中进行的。在西方国家的随机对照试验为参与者提供了一种或两个可修饰的CVD危险因素的参与者,用于测量OS和/或炎症的标记物的参与者。参考列表被手动搜索。偏置工具的Cochrane协作风险用于评估研究质量。搜索策略检索了1248篇文章。审查了纳入纳入标准的19项。八项研究被认为是低偏见的风险。可可黄酮提供给2型糖尿病患者和橄榄油类黄酮,对轻微高血压的女性减少了OS和炎症。其他食物来源效果较弱。观察到对具有各种CVD危险因素的患者的OS和炎症对OS和炎症的效果无一致。研究异质性对学习间比较构成挑战。严格设计的研究将有助于确定黄酮类化干预的有效性,以减少CVD风险的患者的OS和炎症。

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