Dysregulated fatty acid metabolism in coronary ectasia: An extended lipidomic analysis. (1st February 2017)
- Record Type:
- Journal Article
- Title:
- Dysregulated fatty acid metabolism in coronary ectasia: An extended lipidomic analysis. (1st February 2017)
- Main Title:
- Dysregulated fatty acid metabolism in coronary ectasia: An extended lipidomic analysis
- Authors:
- Boles, Usama
Pinto, Rui Climaco
David, Santosh
Abdullah, Abdullah S
Henein, Michael Y - Abstract:
- Abstract: Background: Coronary artery ectasia (CAE) is not an uncommon clinical condition, which could be associated with adverse outcome. The exact pathophysiology of the disease is poorly understood and is commonly interpreted as a variant of atherosclerosis. In this study, we sought to undertake lipidomic profiling of a group of CAE patients in an attempt to achieve better understanding of its disturbed metabolism. Methods: Untargeted lipid profiling and complementary modelling strategies were employed to compare serum samples from 16 patients with CAE (mean age 63.5 ± 10.1 years, 6 female) and 26 controls with normal smooth coronary arteries (mean age 59.2 ± 6.6 years and 7 female). Sample preparation, LC-MS analysis and metabolite identification were performed at the Swedish Metabolomics Centre, Umeå, Sweden. Results: Phosphatidylcholine levels were significantly distorted in the CAE patients (p = 0.001–0.04). Specifically, 16-carbon fatty acyl chain phosphatidylcholines (PC) were detected in lower levels. Similarly, 11 meioties of Sphyngomyelin (SM) species were detected at lower concentrations (p = 0.000001–0.01) in the same group. However, only three metabolites were significantly higher in the pure CAE subgroup (6 patients) when compared with the 10 mixed CAE patients (two meioties of SM species and one of PC). Atherosclerosis risk factors were not different between groups. Conclusion: This is the first lipid profiling study reported in coronary artery ectasia.Abstract: Background: Coronary artery ectasia (CAE) is not an uncommon clinical condition, which could be associated with adverse outcome. The exact pathophysiology of the disease is poorly understood and is commonly interpreted as a variant of atherosclerosis. In this study, we sought to undertake lipidomic profiling of a group of CAE patients in an attempt to achieve better understanding of its disturbed metabolism. Methods: Untargeted lipid profiling and complementary modelling strategies were employed to compare serum samples from 16 patients with CAE (mean age 63.5 ± 10.1 years, 6 female) and 26 controls with normal smooth coronary arteries (mean age 59.2 ± 6.6 years and 7 female). Sample preparation, LC-MS analysis and metabolite identification were performed at the Swedish Metabolomics Centre, Umeå, Sweden. Results: Phosphatidylcholine levels were significantly distorted in the CAE patients (p = 0.001–0.04). Specifically, 16-carbon fatty acyl chain phosphatidylcholines (PC) were detected in lower levels. Similarly, 11 meioties of Sphyngomyelin (SM) species were detected at lower concentrations (p = 0.000001–0.01) in the same group. However, only three metabolites were significantly higher in the pure CAE subgroup (6 patients) when compared with the 10 mixed CAE patients (two meioties of SM species and one of PC). Atherosclerosis risk factors were not different between groups. Conclusion: This is the first lipid profiling study reported in coronary artery ectasia. While the lower concentration and dysregulation of sphyngomyelin suggests an evidence for premature apoptosis, that of phosphatidylcholines suggests perturbed fatty acid elongation/desaturation, thus may be indicative of non-atherogenic process in CAE. … (more)
- Is Part Of:
- International journal of cardiology. Volume 228(2017)
- Journal:
- International journal of cardiology
- Issue:
- Volume 228(2017)
- Issue Display:
- Volume 228, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 228
- Issue:
- 2017
- Issue Sort Value:
- 2017-0228-2017-0000
- Page Start:
- 303
- Page End:
- 308
- Publication Date:
- 2017-02-01
- Subjects:
- Coronary artery ectasia -- Lipidomic analysis -- Phosphatidylcholine -- Sphyngeomyeline -- Atherosclerosis
Cardiology -- Periodicals
Electronic journals
616.12 - Journal URLs:
- http://www.clinicalkey.com/dura/browse/journalIssue/01675273 ↗
http://www.sciencedirect.com/science/journal/01675273 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ijcard.2016.11.093 ↗
- Languages:
- English
- ISSNs:
- 0167-5273
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.158000
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