Abstract | AIMS: METHODS AND RESULTS: The plasma proteome of 50 patients with heart failure who died or were rehospitalised were compared with 50 patients with heart failure, matched for age and sex, who did not have an event. Peptides were analysed on two-dimensional liquid chromatography coupled to tandem mass spectrometry (2D LC ESI-MS/MS) in high definition mode (HDMSE). We identified and quantified 3001 proteins, of which 51 were significantly up-regulated and 46 down-regulated with more than two-fold expression changes in those who experienced death or rehospitalisation. Gene ontology enrichment analysis and protein-protein interaction networks of significant differentially expressed proteins discovered the central role of metabolic processes in clinical outcomes of patients with heart failure. The findings revealed that a cluster of proteins related to glutathione metabolism, arginine and proline metabolism, and pyruvate metabolism in the pathogenesis of poor outcome in patients with heart failure who died or were rehospitalised. CONCLUSIONS:
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Authors | Thong H Cao, Donald J L Jones, Adriaan A Voors, Paulene A Quinn, Jatinderpal K Sandhu, Daniel C S Chan, Helen M Parry, Mohapradeep Mohan, Ify R Mordi, Iziah E Sama, Stefan D Anker, John G Cleland, Kenneth Dickstein, Gerasimos Filippatos, Hans L Hillege, Marco Metra, Piotr Ponikowski, Nilesh J Samani, Dirk J Van Veldhuisen, Faiez Zannad, Chim C Lang, Leong L Ng |
Journal | European journal of heart failure
(Eur J Heart Fail)
Vol. 22
Issue 1
Pg. 70-80
(01 2020)
ISSN: 1879-0844 [Electronic] England |
PMID | 31692186
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2019 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. |
Chemical References |
- Angiotensin Receptor Antagonists
- Angiotensin-Converting Enzyme Inhibitors
- Proteome
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Topics |
- Aged
- Aged, 80 and over
- Angiotensin Receptor Antagonists
- Angiotensin-Converting Enzyme Inhibitors
- Disease Progression
- Female
- Heart Failure
(therapy)
- Humans
- Male
- Percutaneous Coronary Intervention
- Plasma
- Proteome
- Proteomics
- Stroke Volume
- Tandem Mass Spectrometry
- Ventricular Function, Left
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