| Literature DB >> 24832990 |
Zhang Lin1, Carlos M Vicente Gonçalves2, Ling Dai1, Hong-mei Lu3, Jian-hua Huang4, Hongchao Ji1, Dong-sheng Wang5, Lun-zhao Yi1, Yi-zeng Liang1.
Abstract
Metabolic syndrome (MetS) is a constellation of the most dangerous heart attack risk factors: diabetes and raised fasting plasma glucose, abdominal obesity, high cholesterol and high blood pressure. Analysis and representation of the variances of metabolic profiles is urgently needed for early diagnosis and treatment of MetS. In current study, we proposed a metabolomics approach for analyzing MetS based on GC-MS profiling and random forest models. The serum samples from healthy controls and MetS patients were characterized by GC-MS. Then, random forest (RF) models were used to visually discriminate the serum changes in MetS based on these GC-MS profiles. Simultaneously, some informative metabolites or potential biomarkers were successfully discovered by means of variable importance ranking in random forest models. The metabolites such as 2-hydroxybutyric acid, inositol and d-glucose, were defined as potential biomarkers to diagnose the MetS. These results obtained by proposed method showed that the combining GC-MS profiling with random forest models was a useful approach to analyze metabolites variances and further screen the potential biomarkers for MetS diagnosis.Entities:
Keywords: Biomarker; GC–MS; Metabolic syndrome; Random forest; Serum profiling
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Year: 2014 PMID: 24832990 DOI: 10.1016/j.aca.2014.04.008
Source DB: PubMed Journal: Anal Chim Acta ISSN: 0003-2670 Impact factor: 6.558