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不稳定型心绞痛的生物标志物及养心汤干预:一项血浆的探索性代谢组学研究

Biomarkers of unstable angina pectoris and yangxin decoction intervention: An exploratory metabonomics study of blood plasma.

作者信息

Yu Xiao-Hong, Sun Jing, Wang Yan, Zhou Ya-Bin

机构信息

Second Department of Cardiovascular, The First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, China.

出版信息

Medicine (Baltimore). 2017 May;96(21):e6998. doi: 10.1097/MD.0000000000006998.

DOI:10.1097/MD.0000000000006998
PMID:28538412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5457892/
Abstract

BACKGROUND

This study aimed to explore the related metabolic biomarkers and to observe the effects of Yangxin Decoction (YXD) on plasma metabolism of patients with unstable angina (UA).

METHODS

In total, 10 patients with UA (intervention group) and 10 healthy participants (control group) were recruited for this study from January 2009 to December 2010. Plasma samples from both groups were analyzed using liquid chromatography mass spectrometry (LC-MS). Principle component analysis (PCA) and partial least squares (PLS) were used to explore the correlations between metabolic markers in patients with UA.

RESULTS

The LC-MS results indicated that the serum levels of 5 potential metabolic markers, namely, ceramide, glycocholic acid, allocholic acid, lithocholic acid, and leukotriene (LT) B4, were significantly higher in the intervention group than those in the control group.

CONCLUSION

The results of this study demonstrated potential metabolic markers that can be used to distinguish and diagnose patients with UA.

摘要

背景

本研究旨在探索相关代谢生物标志物,并观察养心汤(YXD)对不稳定型心绞痛(UA)患者血浆代谢的影响。

方法

2009年1月至2010年12月,本研究共招募了10例UA患者(干预组)和10名健康参与者(对照组)。两组的血浆样本均采用液相色谱质谱联用仪(LC-MS)进行分析。主成分分析(PCA)和偏最小二乘法(PLS)用于探索UA患者代谢标志物之间的相关性。

结果

LC-MS结果表明,干预组中5种潜在代谢标志物,即神经酰胺、甘氨胆酸、别胆酸、石胆酸和白三烯(LT)B4的血清水平显著高于对照组。

结论

本研究结果证明了可用于区分和诊断UA患者的潜在代谢标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/e6e0efc50cdc/medi-96-e6998-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/394af681950f/medi-96-e6998-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/b83384f8d41c/medi-96-e6998-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/32cb4ca76e10/medi-96-e6998-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/f65c1e649494/medi-96-e6998-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/955aa56e2920/medi-96-e6998-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/48e925086bdf/medi-96-e6998-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/e6e0efc50cdc/medi-96-e6998-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/394af681950f/medi-96-e6998-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/b83384f8d41c/medi-96-e6998-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/32cb4ca76e10/medi-96-e6998-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/f65c1e649494/medi-96-e6998-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/955aa56e2920/medi-96-e6998-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/48e925086bdf/medi-96-e6998-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee8/5457892/e6e0efc50cdc/medi-96-e6998-g010.jpg

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