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首页> 外文期刊>RSC Advances >A pseudo-kinetics approach for time-series metabolomics investigations: more reliable and sensitive biomarkers revealed in vincristine-induced paralytic ileus rats
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A pseudo-kinetics approach for time-series metabolomics investigations: more reliable and sensitive biomarkers revealed in vincristine-induced paralytic ileus rats

机译:用于时间序列代谢组织调查的伪动力学方法:在血管氨基诱导的麻痹性嗜血浴大鼠中显示更可靠和敏感的生物标志物

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摘要

Time-series metabolomics studies can provide snapshots of the metabolic status during the progress of disease and drug treatment. In order to reveal the dynamic development of a disease, a pseudo-kinetics approach based on calibration and integration of absolute fold changes (FCk) along the time points was proposed. A distance based discriminative trajectory was applied to assess global metabolic alterations during ileus progress upon principle component analysis (PCA). The area under the curve (AUC) and peak time (T-max) of the absolute FCk-time curve were integrated as complementary thresholds to screen sensitive biomarkers compared with the typical ileus parameters of gastric emptying (GE) and gastrointestinal transit (GI). As a result, docosahexaenoic acid, glycocholic acid, glutamine and acetylcarnitine were identified as sensitive biomarkers for early prediction of paralytic ileus, which were related to intestinal inflammation and mucosal injury. Furthermore, the discrimination abilities of these four biomarkers were validated using receiver-operating characteristic (ROC) analysis. Collectively, this study demonstrated that our proposed pseudo-kinetics approach is effective to screen more reliable and sensitive biomarkers along a pathologic progress.
机译:时间序列代谢组学研究能够疾病和药物治疗的进展过程中提供的代谢状态的快照。为了揭示疾病的发展动态,伪动力学方法基于校准和沿时间点绝对倍数变化(FCK)的集成提出。基于距离判别轨迹应用在主成分分析(PCA)肠梗阻的进展,以评估全球代谢改变。 (AUC)的曲线下面积和峰时间(T-MAX)的绝对FCK - 时间曲线被集成为互补的阈值与胃排空(GE)和胃肠道运输(GI)的典型肠梗阻参数相比屏幕敏感的生物标志物。其结果是,二十二碳六酸,甘氨胆酸,谷氨酰胺和乙酰被确定为麻痹性肠梗阻,将其相关的肠道炎症和粘膜损伤的早期预测敏感生物标志物。此外,这四个生物标志物的鉴别能力利用接受者操作特性(ROC)分析进行了验证。总的来说,这项研究表明,我们提出的伪动力学的方法是有效的屏幕更可靠,沿病变的进展敏感的生物标志物。

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  • 来源
    《RSC Advances》 |2016年第59期|共8页
  • 作者单位

    China Pharmaceut Univ Key Lab Drug Qual Control &

    Pharmacovigilance Minist Educ Nanjing 210009 Jiangsu Peoples R China;

    China Pharmaceut Univ Key Lab Drug Qual Control &

    Pharmacovigilance Minist Educ Nanjing 210009 Jiangsu Peoples R China;

    China Pharmaceut Univ Key Lab Drug Qual Control &

    Pharmacovigilance Minist Educ Nanjing 210009 Jiangsu Peoples R China;

    Macau Univ Sci &

    Technol State Key Lab Qual Res Chinese Med Taipa Macau Peoples R China;

    China Pharmaceut Univ Key Lab Drug Qual Control &

    Pharmacovigilance Minist Educ Nanjing 210009 Jiangsu Peoples R China;

    China Pharmaceut Univ Key Lab Drug Qual Control &

    Pharmacovigilance Minist Educ Nanjing 210009 Jiangsu Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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