Metabolomics and partial least square discriminant analysis to predict history of myocardial infarction of self-claimed healthy subjects: validity and feasibility for clinical practice.

Journal of clinical bioinformatics Pub Date : 2015-03-13 eCollection Date: 2015-01-01 DOI:10.1186/s13336-015-0018-4
Nornazliya Mohamad, Rose Iszati Ismet, MohdSalleh Rofiee, Zakaria Bannur, Thomas Hennessy, Manikandan Selvaraj, Aminuddin Ahmad, FadzilahMohd Nor, ThuhairahHasrah Abdul Rahman, Kamarudzaman Md Isa, AdzroolIdzwan Ismail, Lay Kek Teh, Mohd Zaki Salleh
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引用次数: 14

Abstract

Background: The dynamics of metabolomics in establishing a prediction model using partial least square discriminant analysis have enabled better disease diagnosis; with emphasis on early detection of diseases. We attempted to translate the metabolomics model to predict the health status of the Orang Asli community whom we have little information. The metabolite expressions of the healthy vs. diseased patients (cardiovascular) were compared. A metabotype model was developed and validated using partial least square discriminant analysis (PLSDA). Cardiovascular risks of the Orang Asli were predicted and confirmed by biochemistry profiles conducted concurrently.

Results: Fourteen (14) metabolites were determined as potential biomarkers for cardiovascular risks with receiver operating characteristic of more than 0.7. They include 15S-HETE (AUC = 0.997) and phosphorylcholine (AUC = 0.995). Seven Orang Asli were clustered with the patients' group and may have ongoing cardiovascular risks and problems. This is supported by biochemistry tests results that showed abnormalities in cholesterol, triglyceride, HDL and LDL levels.

Conclusions: The disease prediction model based on metabolites is a useful diagnostic alternative as compared to the current single biomarker assays. The former is believed to be more cost effective since a single sample run is able to provide a more comprehensive disease profile, whilst the latter require different types of sampling tubes and blood volumes.

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代谢组学和偏最小二乘判别分析预测自称健康受试者心肌梗死史:临床实践的有效性和可行性
背景:利用偏最小二乘判别分析建立代谢组学的动态预测模型,可以更好地进行疾病诊断;强调疾病的早期发现。我们试图翻译代谢组学模型来预测我们知之甚少的原住民社区的健康状况。比较健康和患病患者(心血管)的代谢物表达。利用偏最小二乘判别分析(PLSDA)建立了代谢型模型并进行了验证。同时进行的生物化学分析预测和证实了猩猩的心血管风险。结果:14种代谢物被确定为心血管风险的潜在生物标志物,受试者工作特征大于0.7。其中15S-HETE (AUC = 0.997)和磷酸胆碱(AUC = 0.995)。7只猩猩与患者组聚集在一起,可能有持续的心血管风险和问题。生物化学测试结果显示胆固醇、甘油三酯、高密度脂蛋白和低密度脂蛋白水平异常,这也支持了这一观点。结论:与目前的单一生物标志物分析相比,基于代谢物的疾病预测模型是一种有用的诊断选择。前者被认为更具成本效益,因为单次取样能够提供更全面的疾病概况,而后者需要不同类型的采样管和血容量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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