- Open Access
Blood metabolomic fingerprint is distinct in healthy coronary and in stenosing or microvascular ischemic heart disease
Journal of Translational Medicine volume 15, Article number: 112 (2017)
The endothelium is a key variable in the pathogenesis of atherosclerosis and its complications, particularly coronary artery disease (CAD). Current evidence suggests that the endothelial status can be regarded as an integrated index of individual atherogenic and anti-atherogenic properties, and that the interaction between circulating factors and the arterial wall might be critical for atherogenesis. In organism-level investigations, a functional view is provided by metabolomics, the study of the metabolic profile of small molecules. We sought to verify whether metabolomic analysis can reveal the presence of coronary microenvironment peculiarities associated with distinct manifestations of CAD.
Thirty-two coronary blood samples were analyzed using 1H-NMR-based metabolomics. Samples collected from patients with evidence of myocardial ischemia formed the case group, and were further divided into the stenotic-disease (SD) group (N = 13) and absence of stenosis (microvascular disease; “Micro”) group (N = 8); specimens of patients presenting no evidence of ischemic heart disease (dilated cardiomyopathy, valvular diseases) constituted the control group (N = 11).
Application of an orthogonal partial least squares discriminant analysis (OPLS-DA) model to the entire dataset clearly separated the samples into 3 groups, indicating 3 distinct metabolic fingerprints. Relative to control-group members, Micro patients showed a higher content of 2-hydroxybutirate, alanine, leucine, isoleucine, and N-acetyl groups and lower levels of creatine/phosphocreatine, creatinine, and glucose, whereas SD patients showed higher levels of 3-hydroxybutirate and acetate and a lower content of 2-hydroxybutirate. Moreover, relative to SD patients, Micro patients showed higher levels of 2-hydroxybutirate, alanine, leucine, and N-acetyl groups and lower levels of 3-hydroxybutirate and acetate.
Specific coronary microenvironments are likely associated with distinct development and pathological expression of CAD.
Atherosclerosis is currently the leading cause of death and disability in developing countries and is mainly expressed in the form of coronary artery disease (CAD), which is associated with high morbidity and mortality [1, 2].
Although systemic cardiovascular risk factors for atherosclerosis (hyperlipidemia, diabetes mellitus, smoking and hypertension) have been identified [3,4,5,6,7,8,9], a wide series of researches suggest that the local microenvironment, that comprehends arterial mechanics, matrix remodelling and lipid deposition, plays a key role in regulating the susceptibility to plaque development and progression, regulating the function of endothelial cells. Moreover, these microenvironmental stimuli are capable of modulate other aspects of the microenvironment through collective adaptation . All these events induce a series of biochemical reactions that generate a wide and complex interplay between metabolites absorbed from or released in blood , thus modifying also the vascular microenvironment.
In this context, the omics approach could represent an innovative method for comprehensively investigating the molecular basis of CAD pathogenesis.
During the past decade, both animal and human studies have enabled the rapid development of metabolomics. By combining targeted and non-targeted approaches, metabolomic analysis has identified small-molecule metabolite profiles of diverse cardiovascular risk factors and diseases [11,12,13].
On this basis, our hypothesis was that (i) despite similar cardiovascular risk factors, coronary different microenvironments, generated by interaction between inherited and acquired factors, could generate distinct manifestations of CAD and (ii) these microenvironmental differences might be investigated by metabolomics analysis.
The study was approved by the Institutional Ethics Committee (Azienda Ospedaliero-Universitaria of Cagliari) and was performed in accordance with the Declaration of Helsinki.
We consecutively enrolled patients requiring coronary angiography among those screened in our clinic; they were informed of the purpose and methodology of the study and their written consent was obtained prior to inclusion. They underwent a complete cardiovascular assessment, which included medical history evaluation, physical examination, blood pressure measurement, 12-lead electrocardiogram and echocardiogram, in accordance with the American Society of Echocardiography/European Association of Cardiovascular Imaging guidelines . The patients were also submitted to a physical or pharmacological stress test, in order to confirm/exclude the diagnosis of angina. The patients with myocardial ischemia confirmed by provocative testing formed the case group, and were further subdivided, on the basis of coronary angiography, in patients with stenotic disease (SD group; N = 13) and without stenosis (microvascular disease, “Micro” group; N = 8). Patients with indications for coronary angiography different from angina/myocardial infarction (i.e. dilated cardiomyopathy, valvular disease), normal coronary angiogram and no evidence of atherosclerotic lesions in other vascular district constituted the control group (N = 11). In total, thirty-two coronary blood samples were collected. Table 1 lists the full inclusion and exclusion criteria.
In Table 2, the anthropometric and clinical data of the patients are summarized; no significant differences were present among the 3 groups.
All participants underwent a coronary angiography, during which a blood sample was collected after a good insertion of the diagnostic catheter into the coronary ostium and before performing any procedure on the vessel. The examinations were performed in accordance with specific published guidelines . Arterial blood was aspirated through the catheter by a 5 mL syringe, stored in heparinized tube and maintained at 4 °C until it was centrifuged at 4000 rpm for 15′ and aliquoted in 800 μL cuvettes. Plasma samples were then stored at −80 °C. The contrast medium used was iomeprol (Iomeron®, Bracco U.K. Ltd).
Plasma sample preparation and 1H-NMR spectroscopy
Each plasma sample was thawed and centrifuged at 4500 rpm at 4 °C for 10 min, and then 800 μL of the plasma was dissolved in 2.4 mL of a chloroform/methanol mixture (1:1, v/v) and 350 mL of H2O; the solution was centrifuged at 4500 rpm at 4 °C for 30 min. The resulting ~1 mL of the hydrophilic phase, which contained the low-molecular-weight water-soluble components, was separated from the lipophilic phase, dried using a vacuum concentrator (Eppendorf), and stored at −80 °C. Before NMR analysis, the dried hydrophilic plasma extracts were re-dissolved in 700 μL of D2O (99.8%, Cambridge Isotope Laboratories Inc., Andover, MA, USA) and a 630-μL aliquot was transferred into 5-mm-O.D NMR tubes, to which 70 μL of TSP [3-(trimethylsilyl)propanoic acid] was added as the internal standard (98 atom% D, Sigma-Aldrich, Milan, Italy).
1H-NMR experiments were conducted using a Varian UNITY INOVA 500 spectrometer operating at 499,839 MHz for protons and equipped with a 5-mm double-resonance probe (Agilent Technologies, Santa Clara, CA, USA). 1H-NMR spectra were acquired at 300 K with a spectral width of 6000 Hz, a 90° pulse, an acquisition time of 2 s, a relaxation delay of 2 s, and 256 scans. A presaturation sequence was used to suppress the residual H2O signal by applying low-power selective irradiation at the H2O frequency during the recycle delay. Moreover, 1H–1H COSY 2D NMR spectra were acquired. The experiment was performed by using a spectral width of 6000 Hz in both dimensions, 2048 data points, and 512 increments with 32 transients per increment. The COSY experiment was conducted using a gradient-selected coherence transfer pathway (gCOSY).
Data processing and statistical analysis
1H-NMR spectra were imported into ACDlab Processor Academic Edition (Advanced Chemistry Development, 12.01, 2010) and pre-processed with a line-broadening of 0.3 Hz, zero-filled to 64 K, and Fourier transformed. Each spectrum was manually phased and baseline-corrected. Chemical shifts were referred to the TSP single resonance at 0.00 ppm. The spectra were then imported into MATLAB (R2013b; Mathworks, Inc., Natick, MA, USA), where the spectra were aligned using Interval Correlation Optimized Shifting (icoshift)  to correct for small peak misalignments of certain metabolites. The spectral region between 4.74 and 4.94 ppm was excluded from the analysis in order to remove the effect of variations in the presaturation of the residual water resonance. Lastly, the spectral dataset was normalized to the total area in order to minimize the effects of variable concentration among distinct samples, and then imported into the SIMCA-P+ program (Version 13.0, Umetrics, Malmö, Sweden) for multivariate statistical analysis. Data were Pareto scaled and subjected to Hotelling’s T2 and DModX tests in order to verify the presence of potential outliers. Orthogonal partial least squares discriminant analysis (OPLS-DA), a supervised method, was used to build models and identify the variables that can discriminate between patients and controls. Since OPLS-DA can lead to over-fit models, particularly with few samples as in the present study, we verified the model quality by performing a sevenfold cross-validation and permutation test 400 times on the corresponding partial least square discriminant analysis (PLS-DA) model. Overfitting and predictive ability of the models were assessed using R2 and Q2 values. To evaluate the differences in metabolites between the 3 groups, a parametric Student’s test (with P values corrected with the Bonferroni method) was performed on the relative concentration of the NMR signals determined using Chenomx NMR suite 7.1 (Chenomx Inc., Edmonton, AB, Canada). The receiver operating-characteristic (ROC) curve was analyzed with sensitivity versus 1—specificity, and the area under the curve (AUC) was calculated using the free software package ROCCET: ROC Curve Explorer and Tester (http://metaboanalyst.ca/faces/Secure/upload/RocUploadView.xhtml) . An AUC >0.8 indicates a test exhibiting good discrimination between controls and patients.
In accordance with the inclusion/exclusion criteria, the control-group patients showed no coronary stenosis or alterations in the TIMI angiographic flow grades. The patients in the Micro group exhibited no coronary atherosclerotic lesions, but presented a low (1–2) TIMI flow grade and, in one case, coronary spasm induced by catheter irrigation. By contrast, the angiographic findings revealed that the SD group included 2 patients with significant (>75% diameter stenosis or FFR <80%) monovascular disease, 6 with bivascular disease, and 5 with left main/trivascular disease.
The metabolites were identified with the aid of the literature and databases such as Human Metabolome Database (HMDB, http://www.hmdb.ca) and the 500-MHz library from Chenomx NMR suite 7.1. The attribution of the major peaks of the plasma samples are shown in Fig. 1, whereas the chemical shifts of all metabolites are summarized in Table 3. In addition to the signals due to the metabolites, such as amino acids, sugars, and organic acids from the plasma, the spectra displayed a series of extremely intense resonances in the region between 3.1 and 4.2 ppm; these do not belong to the physiological metabolic profile of the plasma but to the contrast agent employed in the standard procedure of arterial blood collection. Both 1D and 2D NMR experiments were conducted on a solution of the contrast agent (Fig. 2; Additional file 1: Figure S1), which allowed discrimination of its characteristic resonances, and these were then excluded from the statistical analysis performed on the plasma spectra.
First, an OPLS-DA model was applied to the entire dataset; the results obtained (Fig. 3) showed that the samples were clearly separated into 3 groups, which indicated that the controls and the Micro and SD patients presented highly distinct metabolic profiles. The OPLS-DA model was established using 2 predictive components and one orthogonal component, and showed good values of R2Y and Q2 (Table 4). To validate the OPLS-DA model, a permutation test on the corresponding PLS-DA model was performed using the same number of components. The results (Table 4) clearly indicated that the OPLS-DA model was statistically valid. Three separate OPLS-DA models were built using the same 3 groups of samples—Control, Micro, and SD—but only 2 groups were compared in each case. The results of these pairwise comparisons (Fig. 4) enabled improved assessment and identification of the metabolites that were responsible for the separation between the distinct groups. The parameters for all OPLS-DA models are summarized in Table 4. In addition to the permutation test, a cross-validated score plot for the same OPLS-DA models was created (Additional file 2: Figure S2), because an external test dataset was not present. In the cross-validated score plot of SD versus Control, 2 SD and 2 Control samples were misclassified, whereas all the other samples were accurately classified within their groups. The metabolites primarily responsible for group separation were finally identified by building a V-plot for each OPLS-DA model (Additional file 3: Figure S3). The V-plot reveals the contribution of each variable to the predictive component, matching the correlation coefficients p(corr) and VIP values, and the VIP value is used to evaluate the variables’ relative importance. Here, variables (metabolites) with a VIP score of >1 were considered and their relative concentration was determined using Chenomx NMR suite 7.1, and the new dataset thus obtained was normalized and subjected to Student’s test and the results were corrected with the Bonferroni method. The “fold-change” was calculated for each of these variables and its magnitude was color-coded based on the corresponding P value from the Student’s test (Fig. 5). Several metabolites were found to change significantly among the 3 groups of samples. With respect to control patients, a higher content of 2-hydroxybutirate, alanine, leucine, isoleucine, N-acetyl groups and a lower content of creatine/phosphocreatine, creatinine, and glucose characterized the Micro patients (Fig. 5a), whereas a higher content of 3-hydroxybutirate and acetate and a lower content of 2-hydroxybutirate characterized the SD patients (Fig. 5b). Lastly, a complementary comparison between the Micro and SD patients (Fig. 5c) revealed a higher content of 2-hydroxybutirate, alanine, leucine, and N-acetyl groups and a lower content of 3-hydroxybutirate and acetate in the Micro group. ROC curves were created to assess the combined performance (significance) of these metabolites; the relative concentration of the metabolites allowed discrimination of the 3 groups, with the area under the ROC curve (AUC) >0.9 for each pair.
We conducted a pathophysiological study to identify possible metabolic differences in the microenvironment of coronary arteries, normal or suffering from both stenotic and microvascular disease, using metabolomics, an innovative and highly sensitive method.
For this purpose, we conducted 1H-NMR experiments on blood samples obtained from coronary artery of all enrolled case-group and control patients. We obtained the following results: (1) the OPLS-DA model used here separated the samples into 3 groups, which indicated that, given comparable cardiovascular risk factors, the controls and the Micro and SD patients were characterized by markedly different metabolic profiles. (2) ROC curves, created to evaluate the importance of the relative concentration of detected metabolites, confirmed the identification of the 3 distinct biochemical fingerprints, one belonging to healthy coronary arteries, the other 2 underlying the stenotic and microvascular manifestations of CAD. (3) Pairwise comparisons used to identify the metabolites responsible for the separation among groups revealed that relative to the control group, the Micro group showed higher levels of 2-hydroxybutyrate, alanine, leucine, isoleucine, and N-acetyl groups and lower levels creatine/phosphocreatine, creatinine, and glucose, whereas the SD group showed higher levels of 3-hydroxybutyrate and acetate and lower levels of 2-hydroxybutirate; furthermore, the levels of 2-hydroxybutyrate, alanine, leucine, and N-acetyl groups were higher and those of 3-hydroxybutyrate and acetate lower in the Micro group than in the SD group.
Several studies on the pathophysiological mechanisms involved in atherogenesis have shown that alteration in endothelial function is a key event in the development of this pathology and that it plays a major role in plaque progression and complication [18,19,20,21]. By contrast, with regard to the possibility of using metabolomics for detecting the presence of CAD and defining its severity, previous studies have obtained divergent results, first supporting  and then refuting  the likelihood of this approach being employed effectively.
However, the prevalence of an interest in diagnostics diverted the attention from the endothelium as the substrate of atherogenesis.
The investigation of endothelial metabolic responses is critical: the recognized risk factors for atherosclerosis, although typically systemic, necessarily require an alteration of endothelial properties to change from a potential threat to a pathological lesion [10, 18,19,20].
As stated in the Introduction section, the action of neural, hormonal, paracrine or cytokine signaling directly or indirectly modifies cellular metabolic pathways [11, 24]. Furthermore, it was shown that even the endothelial mechanoreceptors activity can alter circulating metabolites and may be revealed by metabolomics .
Given all the aforementioned considerations, we designed this study to assess the coronary microenvironment and its relationship with the pattern and degree of arterial anatomical and functional impairment in patients undergoing coronary angiography. Patients with stable angina (confirmed by positive stress test) formed the 2 case groups (Micro and SD), whereas patients with non-ischemic diseases (e.g., valvular heart disease, cardiomyopathies) were enrolled as controls. According to our OPLS-DA model, the coronary artery blood of CAD patients with stenosing disease appeared different, with high specificity, from that of patients with microvascular disease. Furthermore, the metabolomic analysis differentiated both case groups from the control group of non-ischemic patients; this discrimination was further confirmed using ROC curves, which validated the OPLS-DA models in terms of sensibility and sensitivity .
The interaction between “macro” risk factors (e.g. diabetes, hypertension, dyslipidaemia) and intrinsic properties (e.g. genetic, epigenetic) of the local endothelial layer may be critical for atherogenesis [10, 26]. This interaction may produce a microenvironment suitable for the phenotypic translation of a specific athero-susceptibility, as previously suggested by a wide range of studies .
The metabolic profile provides a “functional” view of a tissue, intended as the ultimate resultant of its genes, RNAs, proteins and environmental factors (e.g. nutrition). In the case of the endothelium, it may provide evidence of a perturbated blood flow (e.g. the presence of a plaque), reflecting the endpoints of the biological processes of that tissue and the involved pathways [11, 12]. Accordingly, despite the comparable systemic risk factors, all the groups in our study showed different coronary angiography findings and a distinctive metabolic fingerprint, as confirmed by the statistical parameters reported in Table 4. The control group was distinct from both case groups (PC2, Fig. 3), whereas the latter seem to be differentiated along the PC1.
Our results suggest that the normal coronary microenvironment is considerably different from that of coronary arteries affected by both stenotic and microvascular disease. In addition, coronaries with atherosclerosis exhibit different metabolic fingerprints from each other, suggesting the involvement of distinctive pathways in these 2 atherogenic manifestations.
The different expressions or developmental stages of the same disease explained by metabolomics suggest that endothelial dysfunction, though enabled by the classic cardiovascular risk factors, is modulated by other determinants, such as genetic, nutritional and behavioral, and causes various local micro-environments, witnessing an individual sensitivity to atherosclerosis. The cluster of identified metabolites, specific for each group, as confirmed by the ROC curves, suggests the existence of multiple pathways involved in atherosclerotic development and responsible for the differences we encountered.
Coronary blood from the SD group contained higher levels of acetoacetate and 3-hydroxybutyrate but lower levels of 2-hydroxybutyrate than did the blood from both Micro and Control groups. Acetoacetate and 3-hydroxybutyrate, but not 2-hydroxybutyrate, have been associated with atherogenesis in diabetic patients [27, 28]. Specifically, Kanikarla-Marie and Jain showed that these 2 ketone bodies upregulate NADPH oxidase and thus cause, at the endothelial level, an increase in oxidative stress, ICAM-1 expression, and monocyte adhesion , all of which are involved in atherosclerosis development.
Relative to controls, Micro patients showed elevated levels of alanine, leucine/isoleucine, 2-hydroxybutyrate, and N-acetyl groups, but lower levels of creatine and creatinine. Creatine exerts anti-inflammatory effects at the endothelial level by inhibiting ICAM-1 and E-selectin expression and thereby reducing neutrophil margination. Furthermore, creatine can reduce endothelial permeability , and Sestili et al. have highlighted the cytoprotective effect of creatine as a radical scavenger against reactive oxygen (in particular hydroxyl radical) and nitrogen species .
Recently, alanine was found to be independently associated with major adverse cardiovascular events,  but reduced alanine levels were also reported in both apolipoprotein E-deficient mice (apolipoprotein E(−/−) mice)  and the plasma of patients with stable carotid atherosclerosis . This dual behavior of alanine (association with cardiovascular events, but reduction in patients with atherosclerosis) was also observed in our study population: alanine levels were higher in Micro patients than in both controls and SD patients, which suggests a risk profile wherein ischemic events are not associated with atherosclerotic plaques. A similar functional behavior was also observed for leucine/isoleucine, which reduced the serum levels of SOD and GPx in hypercholesterolemic rats , but also positively correlated with acetoacetate and 3-hydroxybutyrate in distinguishing atherosclerotic patients from healthy controls .
Vascular endothelial cells maintain the interface between systemic circulation and tissues and mediate several critical processes such as inflammation, coagulation, and homeostasis [10, 18,19,20,21, 26]. Our results show that the metabolic fingerprint of healthy coronary arteries is considerably different from that of atherosclerotic vessels. In addition, the metabolic profile of microvascular dysfunction is distinguishable from that of stenotic disease, despite the presence of comparable cardiovascular risk factors, thereby suggesting different underlying pathways or their different modulation. Surely, complete understanding of this metabolic interaction will require larger studies and the use of integrated (clinical, metabolomic, genomic) approaches. The data gathered from these investigations will improve our understanding of the natural history of the disease. They will help researchers identify new diagnostic tools (i.e. bedside biomarkers assays) and therapeutic targets to modulate endothelial responses and affect the progress of CAD (i.e. coronary stent eluting specific metabolites with demonstrated anti-atherogenic effects on endothelium).
The small number of samples included in this study is certainly a limitation; however, the verification tests and the level of significance seem to confirm the quality of the constructed model. Thus, the involvement of the clustered metabolites in the likelihood of pathophysiologic mechanisms and the solid evidence that the identified metabolites have been associated with cardiovascular events in similar subgroups of patients are significant.
Our study does not pretend to be exhaustive or conclusive, but want to help clarify the reasons for the different individual susceptibility to the development of atherosclerosis, and stimulate further research in this direction.
area under the curve
coronary artery disease
fractional flow reserve
1H-nuclear magnetic resonance
intercellular adhesion molecule
nicotinamide adenine dinucleotide phosphate
orthogonal partial least squares discriminant analysis
partial least squares discriminant analysis
- ROC curve:
receiver operating-characteristic curve
super dioxide dismutase
tissue Doppler imaging
thrombolysis in myocardial infarction
Murray CJ, Lopez AD. Measuring the global burden of disease. N Engl J Med. 2013;369:448–57.
Herrington W, Lacey B, Sherliker P, Armitage J, Lewington S. Epidemiology of atherosclerosis and the potential to reduce the global burden of atherothrombotic disease. Circ Res. 2016;118:535–646.
Weber C, Noels H. Atherosclerosis: current pathogenesis and therapeutic options. Nat Med. 2011;17:1410–22.
Ross R. The pathogenesis of atherosclerosis—an update. New Engl J Med. 1986;314:488–500.
McGill HC Jr. The cardiovascular pathology of smoking. Am Heart J. 1988;115:250–7.
Kannel WB, Gordon T, Schwartz MJ. Systolic versus diastolic blood pressure and risk of coronary heart disease: the Framingham study. Am J Cardiol. 1971;27:335–46.
Kannel WB. Role of blood pressure in cardiovascular morbidity and mortality. Prog Cardiovasc Dis. 1974;17:5–24.
Kannel WB, Castelli WP, Gordon T, McNamara PM. Serum cholesterol, lipoproteins, and the risk of coronary heart disease: the Framingham study. Ann Intern Med. 1971;74:1–12.
Kannel WB, Castelli WP, Gordon T. Cholesterol in the prediction of atherosclerotic disease: new perspectives based on the Framingham study. Ann Intern Med. 1979;90:85–91.
Yurdagul A Jr, Finney AC, Woolard MD, Orr AW. The arterial microenvironment: the where and why of atherosclerosis. Biochem J. 2016;473:1281–95. doi:10.1042/BJ20150844.
Deidda M, Piras C, Bassareo PP, Cadeddu Dessalvi C, Mercuro G. Metabolomics, a promising approach to translational research in cardiology. IJC Metab Endocr. 2015;9:31–8.
Griffin JL, Atherton H, Shockcor J, Atzori L. Metabolomics as a tool for cardiac research. Nat Rev Cardiol. 2011;8:630–43.
Ellis DI, Dunn WB, Griffin JL, Allwood JW, Goodacre R. Metabolic fingerprinting as a diagnostic tool. Pharmacogenomics. 2007;8:1243–66.
Lang RM, Badano LP, Mor-Avi V, Afilalo J, Armstrong A, Ernande L, Flachskampf FA, Foster E, Goldstein SA, Kuznetsova T, Lancellotti P, Muraru D, Picard MH, Rietzschel ER, Rudski L, Spencer KT, Tsang W, Voigt JU. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. Eur Heart J Cardiovasc Imaging. 2015;16:233–70.
Authors/Task Force members, Windecker S, Kolh P, Alfonso F, Collet JP, Cremer J, Falk V, Filippatos G, Hamm C, Head SJ, Jüni P, Kappetein AP, Kastrati A, Knuuti J, Landmesser U, Laufer G, Neumann FJ, Richter DJ, Schauerte P, Sousa Uva M, Stefanini GG, Taggart DP, Torracca L, Valgimigli M, Wijns W, Witkowski A. ESC/EACTS guidelines on myocardial revascularization: the task force on myocardial revascularization of the European Society of Cardiology (ESC) and the European Association for Cardio-Thoracic Surgery (EACTS). Developed with the special contribution of the European Association of Percutaneous Cardiovascular Interventions (EAPCI). Eur Heart J. 2014;35:2541–619.
Savorani F, Tomasi G, Engelsen SB. icoshift: a versatile tool for the rapid alignment of 1D-NMR spectra. J Magn Reson. 2010;202:190–202.
Xia J, Broadhurst DI, Wilson M, Wishart DS. Translational biomarker discovery in clinical metabolomics: an introductory tutorial. Metabolomics. 2013;9:280–99.
Kinlay S, Ganz P. Role of endothelial dysfunction in coronary artery disease and implications for therapy. Am J Cardiol. 1997;80:11I–6I.
Bonetti PO, Lerman LO, Lerman A. Endothelial dysfunction: a marker of atherosclerotic risk. Arterioscler Thromb Vasc Biol. 2003;23:168–75.
Gimbrone MA Jr, Topper JN, Nagel T, Anderson KR, Garcia-Cardeña G. Endothelial dysfunction, hemodynamic forces, and atherogenesis. Ann N Y Acad Sci. 2000;902:230–40.
Gimbrone MA Jr, García-Cardeña G. Endothelial cell dysfunction and the pathobiology of atherosclerosis. Circ Res. 2016;118:620–36.
Brindle JT, Antti H, Holmes E, et al. Rapid and noninvasive diagnosis of the presence and severity of coronary heart disease using 1H-NMR-based metabonomics. Nat Med. 2002;8:1439–44.
Kirschenlohr HL, Griffin JL, Clarke SC, Rhydwen R, Grace AA, Schofield PM, Brindle KM, Metcalfe JC. Proton NMR analysis of plasma is a weak predictor of coronary artery disease. Nat Med. 2006;12:705–10.
McGarrity S, Halldórsson H, Palsson S, Johansson PI, Rolfsson Ó. Understanding the causes and implications of endothelial metabolic variation in cardiovascular disease through genome-scale metabolic modeling. Front Cardiovasc Med. 2016;3:10. doi:10.3389/fcvm.2016.00010.
Go YM, Kim CW, Walker DI, Kang DW, Kumar S, Orr M, Uppal K, Quyyumi AA, Jo H, Jones DP. Disturbed flow induces systemic changes in metabolites in mouse plasma: a metabolomics study using ApoE −/− mice with partial carotid ligation. Am J Physiol Regul Integr Comp Physiol. 2015;308:72.
Aird WC. Mechanisms of endothelial cell heterogeneity in health and disease. Circ Res. 2006;98:159–62.
Li LX, Zhao CC, Ren Y, Tu YF, Lu JX, Wu X, Zhang XZ, Zhu JA, Li MF, Yu LB, Bao YQ, Jia WP. Prevalence and clinical characteristics of carotid atherosclerosis in newly diagnosed patients with ketosis-onset diabetes: a cross-sectional study. Cardiovasc Diabetol. 2013;12:18.
Kanikarla-Marie P, Jain SK. Hyperketonemia (acetoacetate) upregulates NADPH oxidase 4 and elevates oxidative stress, ICAM-1, and monocyte adhesivity in endothelial cells. Cell Physiol Biochem. 2015;35:364–73.
Nomura A, Zhang M, Sakamoto T, Ishii Y, Morishima Y, Mochizuki M, Kimura T, Uchida Y, Sekizawa Y. Anti-inflammatory activity of creatine supplementation in endothelial cells in vitro. Br J Pharmacol. 2003;139:715–20.
Sestili P, Martinelli C, Bravi G, Piccoli G, Curci R, Battistelli G, Falcieri E, Agostini D, Gioacchini AM, Piccoli SG, Curci R, Battistelli M, Falcieri E, Agostini D, Gioacchini AM, Stocchi V. Creatine supplementation affords cytoprotection in oxidatively injured cultured mammalian cells via direct antioxidant activity. Free Radic Biol Med. 2006;40:837–49.
Rizza S, Copetti M, Rossi C, Cianfarani MA, Zucchelli M, Luzi A, Pecchioli C, Porzio O, Di Cola G, Urbani A, Pellegrini F. Metabolomics signature improves the prediction of cardiovascular events in elderly subjects. Atherosclerosis. 2014;232(2):260–4.
Mayr M, Chung YL, Mayr U, Yin X, Ly L, Troy H, Fredericks S, Hu Y, Griffiths JR, Xu Q. Proteomic and metabolomic analyses of atherosclerotic vessels from apolipoprotein E-deficient mice reveal alterations in inflammation, oxidative stress, and energy metabolism. Arterioscler Thromb Vasc Biol. 2005;25:2135–42.
Teul J, Rupérez FJ, Garcia A, Balayssac VS, Gilard V, Malet-Martino M, Martin-Ventura JL, Blanco-Colio ML, Tuñón J, Egido J, Barbas C. Improving metabolite knowledge in stable atherosclerosis patients by association and correlation of GC–MS and 1H NMR fingerprints. J Proteome Res. 2009;8:5580–9.
Cojocaru E, Filip N, Ungureanu C, Filip C, Danciu M. Effects of valine and leucine on some antioxidant enzymes in hypercholesterolemic rats. Health. 2014;6:2313–21.
MD, work conception and design, data analysis and interpretation, paper drafting and final approval; CP, data analysis and interpretation, paper drafting; CCD, work design, data acquisition, analysis and interpretation, paper drafting; DC, work conception and design, data analysis and interpretation; EL, FA, data acquisition, analysis and interpretation; GdC, data acquisition and interpretation, paper revising; MC, data acquisition and interpretation, paper revising; GL, RP, data acquisition and interpretation, paper revising; LA, data analysis and interpretation, paper drafting, revising, final approval; GM, work conception and design, data analysis and interpretation, paper drafting, revising and final approval. All authors read and approved the final manuscript.
For their valuable collaboration, we sincerely thank these Cath Lab members: nurses Francesco Ambu, Andrea Cardia, Andrea Floris, Giorgio Marras, and Ivano Sarritzu; radiology technicians Andrea Puddu, Giampietro Caria, Raimondo Carta, Francesco Moica, and Piera Zampiello; and health-care-assistance operators Gianfranco Congiu, Fausto Melis, and Laura Podda.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The study was approved by the Institutional Ethics Committee (Azienda Ospedaliero-Universitaria, University of Cagliari) and was performed in accordance with the Declaration of Helsinki. Enrolled subjects were informed of the purpose and methodology of the study and their written consent was obtained prior to inclusion.
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NMR 2D-COSY spectrum of Iomeprol (commercial name: Iomeron 350; IUPAC name: N,N’-bis-(2,3-dihydroxypropyl)-5-[(hydroxyacetyl)methylamino]-2,4,6-tri-iodo-1,3-benzenedicarboxamide).
Cross-validated score of OPLSA-DA model derived from the pairwise comparison of 1H NMR spectra of plasma. For each observation, score value from the model (circle) and from the cross validation (box) are shown.
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Deidda, M., Piras, C., Cadeddu Dessalvi, C. et al. Blood metabolomic fingerprint is distinct in healthy coronary and in stenosing or microvascular ischemic heart disease. J Transl Med 15, 112 (2017). https://doi.org/10.1186/s12967-017-1215-7
- Endothelial function
- Coronary artery