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¹H NMR 基于血清代谢组学分析在代偿期和失代偿期肝硬化中的应用。

¹H NMR-based serum metabolic profiling in compensated and decompensated cirrhosis.

机构信息

Key Laboratory of Laboratory Medical Diagnostics, Ministry of Education, Chongqing Medical University, Chongqing 410006, China.

出版信息

World J Gastroenterol. 2012 Jan 21;18(3):285-90. doi: 10.3748/wjg.v18.i3.285.

Abstract

AIM

To study the metabolic profiling of serum samples from compensated and decompensated cirrhosis patients.

METHODS

A pilot metabolic profiling study was conducted using three groups: compensated cirrhosis patients (n = 30), decompensated cirrhosis patients (n = 30) and healthy controls (n = 30). A ¹H nuclear magnetic resonance (NMR)-based metabonomics approach was used to obtain the serum metabolic profiles of the samples. The acquired data were processed by multivariate principal component analysis and orthogonal partial least-squares discriminant analysis (OPLS-DA).

RESULTS

The OPLS-DA model was capable of distinguishing between decompensated and compensated cirrhosis patients, with an R²Y of 0.784 and a Q²Y of 0.598. Twelve metabolites, such as pyruvate, phenylalanine and succinate, were identified as the most influential factors for the difference between the two groups. The validation of the diagnosis prediction showed that the accuracy of the OPLS-DA model was 85% (17/20).

CONCLUSION

¹H NMR spectra combined with pattern recognition analysis techniques offer a new way to diagnose compensated and decompensated cirrhosis in the future.

摘要

目的

研究代偿期和失代偿期肝硬化患者血清样本的代谢轮廓。

方法

采用三组进行初步代谢组学研究:代偿期肝硬化患者(n=30)、失代偿期肝硬化患者(n=30)和健康对照组(n=30)。采用基于¹H 核磁共振(NMR)的代谢组学方法获取样本的血清代谢谱。采用多变量主成分分析和正交偏最小二乘判别分析(OPLS-DA)对获得的数据进行处理。

结果

OPLS-DA 模型能够区分失代偿期和代偿期肝硬化患者,其 R²Y 为 0.784,Q²Y 为 0.598。鉴定出 12 种代谢物,如丙酮酸、苯丙氨酸和琥珀酸,是两组之间差异的最主要影响因素。对诊断预测的验证表明,OPLS-DA 模型的准确率为 85%(17/20)。

结论

¹H NMR 谱结合模式识别分析技术为今后诊断代偿期和失代偿期肝硬化提供了一种新方法。

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