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https://hdl.handle.net/11499/37257
Title: | Serum metabolite profiling of ST-segment elevation myocardial infarction using liquid chromatography quadrupole time-of-flight mass spectrometry | Authors: | Gündogdu, Gülşah Senol, O. Demirkaya Miloglu, F. Koza, Y. Gundogdu, Fuat Hacımüftüoğlu, A. Abd El-Aty, A.M. |
Keywords: | determination LC/Q-TOF/MS/MS metabolomics STEMI alanine arginine betaine butyric acid C reactive protein caffeine carnitine citric acid fumaric acid glycerol glycine high density lipoprotein cholesterol isoleucine lactic acid leucine low density lipoprotein cholesterol lysine maleic acid malonic acid oleic acid palmitic acid phosphatidylethanolamine proline propionic acid serine succinic acid threonine triethanolamine urea valine adult Article body mass cardiovascular risk clinical article controlled study diabetes mellitus female human hyperlipidemia hypertension leukocyte liquid chromatography liquid liquid extraction male metabolic fingerprinting middle aged quadrupole mass spectrometry smoking ST segment elevation myocardial infarction time of flight mass spectrometry |
Publisher: | John Wiley and Sons Ltd | Abstract: | ST segment elevation myocardial infarction (STEMI) is one of the most common global causes of cardiovascular disease-related death. Several metabolites may change during STEMI. Hence, analysis of metabolites in body fluid may be considered as a rapid and accurate test for initial diagnosis. This study has therefore attempted to determine the variation in metabolites identified in the serum of STEMI patients (n = 20) and 15 controls. Samples collected from the Cardiology Department, Medical Faculty, Ataturk University, were extracted by liquid–liquid extraction and analysed using liquid chromatography quadrupole time-of-flight mass spectrometry. The METLIN database was used for the identification and characterization of metabolites. According to Q-TOF/MS measurements, 231 m/z values, which were significantly different between groups (P < 0.01 and fold analysis >1.5) were detected. Metabolite identification was achieved via the Human Metabolome database. According to the multivariate data analysis, leucine, isoleucine, l-proline, l-alanine, glycine, fumaric acid, citrate, succinate and carnitine levels were decreased, whereas levels of propionic acid, maleic acid, butyric acid, urea, oleic acid, palmitic acid, lysoPC [18:2(9Z)], glycerol, phoshpatidylethanolamine, caffeine and l-lactic acid were increased in STEMI patients compared with controls. In conclusion, malonic acid, maleic acid, fumaric acid and palmitic acid can be used as biomarkers for early risk stratification of patients with STEMI. © 2019 John Wiley & Sons, Ltd. | URI: | https://hdl.handle.net/11499/37257 https://doi.org/10.1002/bmc.4738 |
ISSN: | 0269-3879 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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