Impact of type 2 diabetes and the metabolic syndrome on myocardial structure and microvasculature of men with coronary artery disease.

BACKGROUND: Type 2 diabetes and the metabolic syndrome are associated with impaired diastolic function and increased heart failure risk. Animal models and autopsy studies of diabetic patients implicate myocardial fibrosis, cardiomyocyte hypertrophy, altered myocardial microvascular structure and advanced glycation end-products (AGEs) in the pathogenesis of diabetic cardiomyopathy. We investigated whether type 2 diabetes and the metabolic syndrome are associated with altered myocardial structure, microvasculature, and expression of AGEs and receptor for AGEs (RAGE) in men with coronary artery disease.
METHODS: We performed histological analysis of left ventricular biopsies from 13 control, 10 diabetic and 23 metabolic syndrome men undergoing coronary artery bypass graft surgery who did not have heart failure or atrial fibrillation, had not received loop diuretic therapy, and did not have evidence of previous myocardial infarction.
RESULTS: All three patient groups had similar extent of coronary artery disease and clinical characteristics, apart from differences in metabolic parameters. Diabetic and metabolic syndrome patients had higher pulmonary capillary wedge pressure than controls, and diabetic patients had reduced mitral diastolic peak velocity of the septal mitral annulus (E'), consistent with impaired diastolic function. Neither diabetic nor metabolic syndrome patients had increased myocardial interstitial fibrosis (picrosirius red), or increased immunostaining for collagen I and III, the AGE Nε-(carboxymethyl)lysine, or RAGE. Cardiomyocyte width, capillary length density, diffusion radius, and arteriolar dimensions did not differ between the three patient groups, whereas diabetic and metabolic syndrome patients had reduced perivascular fibrosis.
CONCLUSIONS: Impaired diastolic function of type 2 diabetic and metabolic syndrome patients was not dependent on increased myocardial fibrosis, cardiomyocyte hypertrophy, alteration of the myocardial microvascular structure, or increased myocardial expression of Nε-(carboxymethyl)lysine or RAGE. These findings suggest that the increased myocardial fibrosis and AGE expression, cardiomyocyte hypertrophy, and altered microvasculature structure described in diabetic heart disease were a consequence, rather than an initiating cause, of cardiac dysfunction.

Background

Type 2 diabetes and the metabolic syndrome (MetS) are associated with impaired diastolic function and an increased risk of heart failure [1,2]. There is increasing evidence for a specific diabetic cardiomyopathy, independent of coronary artery disease and hypertension, and a similar mechanism may account for the increased heart failure risk associated with the MetS [1-6]. Myocardial fibrosis and cardiomyocyte hypertrophy are the most frequently proposed mechanisms for the impaired diastolic function of diabetes, and morphological changes in small vessels of the diabetic myocardium and reduced capillary length density have also been described [1,2,5]. In addition, advanced glycation end-products (AGEs) are proposed to contribute to diabetic cardiomyopathy by cross-linking myocardial proteins such as collagen and elastin, and by promoting collagen accumulation [7]. Evidence for these mechanisms comes mainly from rodent models of diabetes [7-11], and the increased myocardial fibrosis in rodent models has led to the development of genetic models to examine its pathogenesis and to test antifibrotic therapies [8,9]. There is, however, uncertainty about the role of these mechanisms in the human diabetic heart. There are reports of increased interstitial fibrosis and collagen deposition [12-16], and reports of no difference in fibrosis between diabetic and non-diabetic hearts [17-19], although the impact of diabetes on fibrosis may depend on concomitant hypertension [18]. A key limitation of previous studies of the human diabetic heart is that many were small autopsy studies of end-stage disease that did not allow separation of the effects of diabetes from those of co-morbidities including heart failure and renal disease [3,12,14,16,18,20]. Non-autopsy studies included patients with impaired left ventricular (LV) function and heart failure [17,21-23], and there is uncertainty whether the changes observed were the cause or the consequence of impaired cardiac function.

The present study was undertaken to investigate the association of type 2 diabetes and the MetS with myocardial fibrosis, cardiomyocyte size, capillary length density, diffusion radius, arteriolar dimensions, and myocardial expression of the advanced glycation end-product (AGE) Nε-(carboxymethyl)lysine (CML) and the receptor for AGEs (RAGE). We obtained LV biopsies from patients without heart failure or previous myocardial infarction who were undergoing coronary artery bypass graft surgery. By comparing MetS (pre-diabetic) and diabetic patients with control patients without these conditions, we examined the effects of the insulin-resistant state before diabetes (and anti-diabetes medication) commenced, and the effects of diabetes before heart failure developed. Although we obtained LV biopsies from both men and women, preliminary analysis showed gender-specific differences in myocardial structure [24]; therefore, given the smaller number of women recruited to this study, the present analysis was confined to men.

Methods

Patients

Details of the Cardiac Tissue Bank have been previously described [24]. The St. Vincent's Health Human Research Ethics Committee approved this research and all patients gave written informed consent. From the Tissue Bank we selected all of 46 male patients having coronary artery bypass graft surgery alone, who did not have heart failure or atrial fibrillation, had not received loop diuretic therapy, and did not have evidence of previous myocardial infarction. Absence of previous myocardial infarction was established from the clinical history, electrocardiogram and troponin measurements, and was confirmed by inspection of the ventriculogram, transthoracic and transesophageal echocardiography, and examination of the heart at surgery. All patients had normal or near-normal LV systolic function as assessed by pre-operative transthoracic echocardiography and/or ventriculogram, with LV ejection fraction ≥ 50%. Intra-operative hemodynamics were measured after induction of anesthesia. A partial-thickness wedge-shaped biopsy was taken during surgery, immediately after cardioplegia, from a region of the lateral wall of the LV near the base of the heart, between the territories of the left anterior descending and circumflex arteries, that was free of any macroscopic pathology, without evidence of ischemia or wall motion abnormality on pre-operative or intra-operative imaging studies, as previously described [24].

Of the 46 patients, 13 control patients had neither MetS nor diabetes, 10 had type 2 diabetes, and 23 had MetS. MetS was defined according to the International Diabetes Federation [25]. For patients in whom abdominal circumference was not measured, based on the relationship between abdominal circumference and BMI [26], those with BMI > 25 kg/m2 were considered to exceed the abdominal circumference threshold for MetS. A patient had diabetes if a history of diabetes was evident from use of glucose-lowering medications and/or insulin or if fasting plasma glucose was ≥ 7 mmol/L [27]. Of the 10 patients with diabetes, two were newly diagnosed and treated with diet alone, three were treated with insulin alone, two with insulin and metformin, two with metformin and gliclazide, and one with gliclazide alone. The mean duration of diabetes was 12 (range 0-30) years and the mean HbA1 c was 7.3% (range 5.3-9.8%, n = 7). HbA1 c was not measured routinely as part of patient enrolment in the Tissue Bank, and 3 patients did not have recent HbA1 c measurement before surgery.

Biochemistry

Blood Hb and HbA1c, and plasma levels of creatinine were measured as part of the routine pre-surgery workup. All other variables were measured on fasting blood collected on the day of surgery, before induction of anesthesia. Blood Hb and HbA1c, and plasma levels of glucose, insulin, lipids, and creatinine were measured by St. Vincent's Health Pathology using routine clinical methods. Estimated glomerular filtration rate (eGFR) was calculated from the Modification of Diet in Renal Disease formula [28]. Insulin resistance (HOMA2-IR), insulin sensitivity (HOMA2-%S), and β-cell function (HOMA2-%B), were calculated using the HOMA calculator version 2.2 [29]. CML was measured by ELISA (Microcoat, Penzberg, Germany). Low molecular weight fluorophores (LMWF) were measured by fluorescence spectroscopy [30]. Soluble RAGE was measured by ELISA (R&D Systems Inc., Minneapolis, MN). Amino-terminal-pro-B-type natriuretic peptide (NT-proBNP) was measured by electrochemiluminescence immunoassay using an Elecsys instrument (Roche Diagnostics, Basel, Switzerland).

Histological analysis

Details of tissue collection and fixation have been previously described [24]. All histological analyses were performed blind to patient identity and group allocation. Picrosirius red-stained 4 μm paraffin sections were analyzed for interstitial and perivascular fibrosis and arteriolar dimensions by quantitative morphometry of digitized images of the whole myocardial section (Aperio Technologies, Inc., CA). Myocardial total fibrosis was calculated using the positive pixel count algorithm as the area of collagen staining expressed as a percentage of the total myocardial tissue area, after excluding the pericardium, whereas interstitial fibrosis was calculated as described for total fibrosis, with exclusion of perivascular fibrosis.

Perivascular fibrosis was calculated as the ratio of the area of perivascular fibrosis to the total vessel area (area of vessel wall plus lumen) as determined by planimetry [31], for arterioles with mean diameter (average of maximum and minimum diameter of each arteriole) of 39 μm (range 12-151 μm). Arteriolar wall area/circumference ratio was measured for arterioles with mean average diameters of 20-80 μm. Cardiomyocyte width, determined on 4 μm sections of paraffin-embedded tissue stained for reticulin [32], was the mean of > 100 measurements for each section of the shortest diameter of cardiomyocyte profiles containing a nucleus. Measurement of capillary length density, which is the length of capillaries per unit volume of tissue, has been previously described [24].

Immunohistochemistry for collagen I and collagen III was performed in frozen sections using mouse monoclonal antibodies ab6308 and ab6310 (Abcam, Cambridge, UK), respectively. Myocardial total collagen I and collagen III densities were calculated using the positive pixel count algorithm (Aperio Technologies, Inc., CA) as the area of collagen staining expressed as a percentage of the total myocardial tissue area, after excluding the pericardium. Immunohistochemistry for CML was performed in paraffin sections using a mouse monoclonal antibody as described by Schalkwijk et al. [33]. Immunohistochemistry for RAGE was performed with a goat polyclonal antibody AB5484 (Millipore, Billerica, MA). Immunostaining of arteriolar media and intima for CML and of arteriolar intima and capillaries for RAGE was individually scored by its intensity as 0+, 1+, 2+, or 3+, after inspection of the digitized image of the whole of each section.

Statistical analysis

The significance of differences between study groups was determined by analysis of variance (ANOVA) for continuous variables and Fisher's exact test for categorical variables. Continuous data were logarithmically transformed when necessary to normalize variances. The Fisher's Protected Least Significant Difference test and the Bonferroni correction were used for multiple comparisons of continuous and categorical variables, respectively. Correlations were estimated using Pearson correlation coefficients. All tests were two-tailed. Differences were considered significant at P < 0.05.

Results

Patient characteristics

Patient characteristics are shown in Table 1. The three patient groups were of mean age 63-66 years, with similar extent of coronary artery disease, occluded coronary arteries, collaterals, and numbers of coronary grafts performed. Diabetic patients had increased plasma glucose levels and both MetS and diabetic patients had increased BMI, plasma triglyceride levels, fasting plasma insulin, reduced insulin sensitivity and increased insulin resistance. Diabetic patients also had increased plasma creatinine and reduced eGFR. The three patient groups otherwise had similar clinical and biochemical characteristics, with similar plasma C-reactive protein, NT-proBNP, CML, LMWF, and soluble RAGE levels, and received similar therapies, apart from anti-diabetic therapies.

Table 1

Characteristics of control, metabolic syndrome, and diabetic men undergoing coronary artery bypass graft surgery

Parameter	Control	Metabolicsyndrome	Diabetic
n	13	23	10
Age, years	66 ± 2	63 ± 2	66 ± 3
Left main stenosis > 50%, n (%)	6 (46%)	15 (65%)	3 (30%)
One vessel stenosis > 70%, n (%)	3 (23%)	6 (26%)	1 (10%)
Two vessel stenosis > 70%, n (%)	7 (54%)	11 (48%)	6 (60%)
Three vessel stenosis > 70%, n (%)	3 (23%)	5 (22%)	3 (30%)
Patients with occluded coronary artery, n (%)	5 (38%)	7 (30%)	5 (50%)
Coronary collaterals, Rentrop grade 2 or 3, n (%)	5 (38%)	12 (52%)	5 (50%)
Previous percutaneous transluminal coronary angioplasty, n (%)	2 (15%)	4 (17%)	1 (10%)
Wall motion abnormality, n (%)	2 (15%)	2 (9%)	1 (10%)
Coronary grafts/patient, n	3.4 ± 0.3	3.4 ± 0.2	3.6 ± 0.2
BMI (kg/m2)	25.3 ± 0.8	30.1 ± 0.7*	30.2 ± 1.3†
BSA (m2)	1.93 ± 0.05	2.06 ± 0.03†	2.05 ± 0.06
Clinical risk factors
Pre-admission systolic blood pressure (mmHg)	127 ± 3	134 ± 3	133 ± 4
Pre-admission diastolic blood pressure (mmHg)	74 ± 2	76 ± 2	77 ± 3
Previous hypertension, n (%)	7 (54%)	20 (87%)	8 (80%)
Ever smoked, n (%)	7 (54%)	15 (65%)	6 (60%)
Fasting plasma total cholesterol (mmol/L)	3.5 ± 0.2	3.7 ± 0.3	3.1 ± 0.2
Fasting plasma LDL cholesterol (mmol/L)	2.1 ± 0.2	2.2 ± 0.2	1.7 ± 0.2
Fasting plasma HDL cholesterol (mmol/L)	1.03 ± 0.04	0.93 ± 0.05	0.88 ± 0.06
Fasting plasma triglyceride (mmol/L)	1.08 ± 0.04	2.02 ± 0.21*	1.86 ± 0.26†
Fasting plasma glucose (mmol/L)	5.6 ± 0.2	5.9 ± 0.1	8.1 ± 0.5‡,§
Fasting plasma insulin (pmol/L)	45 ± 11	84 ± 11*	149 ± 53‡
β cell function from HOMA2-%B	65 ± 11	92 ± 9	67 ± 11
Insulin sensitivity from HOMA2-%S	167 ± 22	90 ± 11‡	65 ± 14‡
Insulin resistance from HOMA2-IR	0.8 ± 0.2	1.5 ± 0.2*	2.5 ± 0.7‡
Plasma CML (μmol/L)	2.0 ± 0.2	2.2 ± 0.1	2.2 ± 0.1
Plasma LMWF (AU/mL)	2.6 ± 0.2	2.6 ± 0.2	2.8 ± 0.3
Plasma soluble RAGE (pg/mL)	604 ± 96	642 ± 60	753 ± 108
Plasma NT-proBNP (pmol/L)	16 ± 4	14 ± 2	24 ± 6
Hb (g/L)	14.4 ± 0.3	14.8 ± 0.3	13.3 ± 0.6||
Plasma creatinine (μmol/L)	91 ± 4	91 ± 4	105 ± 4†,||
eGFR (mL/min per 1.73 m2)	74 ± 4	76 ± 3	63 ± 3†,||
C-reactive protein (mg/L)	2.7 ± 0.9	5.5 ± 2.2	3.6 ± 1.2
Medications
ACE inhibitor therapy, n (%)	5 (38%)	11 (48%)	8 (80%)
ARB therapy, n (%)	2 (15%)	8 (35%)	1 (10%)
ACEI and/or ARB therapy, (%)	7 (54%)	18 (78%)	9 (90%)
Statin therapy, n (%)	11 (85%)	20 (87%)	9 (90%)
Aspirin therapy, n (%)	7 (54%)	14 (61%)	5 (50%)
Calcium antagonist therapy, n (%)	2 (15%)	6 (26%)	2 (20%)
β-blocker therapy, n (%)	11 (85%)	15 (65%)	7 (70%)
Long-acting nitrate therapy, n (%)	1 (8%)	4 (17%)	5 (50%)
Thiazide or indapamide therapy, n (%)	3 (23%)	4 (17%)	3 (30%)

Data shown as means ± SEM or n (%). *p < 0.01; †p < 0.05; ‡p < 0.001 in comparison with control; §p < 0.001; ||p < 0.05 in comparison with metabolic syndrome. One metabolic syndrome patient with left main stenosis > 50% did not have other vessel stenosis > 70%. Coronary collaterals were scored according to Rentrop et al. [48]. ARB, angiotensin receptor blocker; CML, Nε-(carboxymethyl)lysine; eGFR, estimated glomerular filtration rate calculated using the Modification of Diet in Renal Disease study equation [28]; HOMA, Homeostasis Model Assessment calculator version 2.2 [29]; LMWF, low molecular weight fluorophore; NT-proBNP, amino-terminal-pro-B-type natriuretic peptide; RAGE, receptor for advanced glycation end-products.

Hemodynamics and echocardiography

Whereas cardiac index was not different between the three patient groups, MetS patients had higher central venous pressure than control patients. Because of the close correlation between central venous pressure and pulmonary capillary wedge pressure (r = 0.80, P < 0.0001), pulmonary capillary wedge pressure data were analyzed with central venous pressure as a covariate, and both MetS and diabetic patients had higher pulmonary capillary wedge pressures than control patients, consistent with impaired diastolic function (Figure 1). Pre-operative transthoracic echocardiography, performed by either the referring institution or by St. Vincent's Health, was not performed in all patients. MetS patients had slightly higher LV ejection fraction than control and diabetic patients (Figure 2). Control, MetS, and diabetic patients had similar left atrial area/body surface area ratio, but diabetic patients had reduced mitral diastolic peak velocity of the septal mitral annulus, E', also consistent with impaired diastolic function. Although the higher mitral Doppler flow velocity E wave/E' ratio of MetS and diabetic patients did not achieve statistical significance, the E/E' ratio for the three patient groups combined correlated with pulmonary capillary wedge pressure (r = 0.44, P = 0.03). There were no differences between the three patient groups with respect to mitral Doppler flow velocity E and A waves, E/A ratio, or mitral deceleration time (data not shown).

Figure 1

Central venous pressure (A), pulmonary capillary wedge pressure (B), and cardiac index (C) in control (Con), metabolic syndrome (MetS), and type 2 diabetic (Diab) men undergoing coronary artery bypass graft surgery. Data shown as means ± SEM. Measurements were made immediately after induction of anesthesia. Pulmonary capillary wedge pressure data were analyzed with central venous pressure as a covariate because of its dependence on central venous pressure.

Figure 2

Ejection fraction (A), left atrial area/body surface area ratio (B), early diastolic peak velocity of the septal mitral annulus, E' (C), and the mitral Doppler flow velocity E wave/E' ratio (D) in control (Con), metabolic syndrome (MetS), and type 2 diabetic (Diab) men undergoing coronary artery bypass graft surgery. Data shown as means ± SEM. Measurements were made by transthoracic echocardiography before surgery.

Total, interstitial and perivascular fibrosis

The mean area of myocardial paraffin sections (3.6-4.8 mm2) was similar for the different patient groups. Total and interstitial fibrosis were similar for the three patient groups, whereas perivascular fibrosis of MetS and diabetic patients was less than in control patients (Figures 3, 4). Total collagen I of diabetic patients was less than for MetS patients, whereas collagen III and the collagen I/collagen III ratio, as assessed by immunohistochemistry, were similar for the three patient groups (Figures 5, 6).

Figure 3

Picrosirius-red staining demonstrating interstitial and perivascular fibrosis (stained red) and arteriolar dimensions (A), reticulin staining of cardiomyocyte membranes demonstrating cardiomyocyte size (B), and CD31 staining of capillaries (C) of left ventricular biopsies from control coronary artery bypass graft surgery patients.

Figure 4

Total myocardial fibrosis (A), interstitial fibrosis (B), and perivascular fibrosis (C) determined by picrosirius red staining in left ventricular biopsies from control (Con), metabolic syndrome (MetS), and type 2 diabetic (Diab) men undergoing coronary artery bypass graft surgery. Data shown as means ± SEM.

Figure 5

Immunostaining for collagen I (A), collagen III (B), and a negative control section without primary antibody (C), of a left ventricular biopsy from a control coronary artery bypass graft surgery patient.

Figure 6

Total collagen I (A), total collagen III (B), and total collagen I/collagen III ratio (C) determined by immunostaining in left ventricular biopsies from control (Con), metabolic syndrome (MetS), and type 2 diabetic (Diab) men undergoing coronary artery bypass graft surgery. Data shown as means ± SEM.

Cardiomyocyte width, capillary length density, and arteriolar dimensions

Cardiomyocyte width, capillary length density, and diffusion radius did not differ between control, MetS and diabetic patients (Figures 3, 7). Arteriolar wall area/circumference ratio was measured for arterioles with diameters (average of maximum and minimum diameters for each arteriole) of 20-80 μm; mean average arteriolar diameters were 36-37 μm. There were no differences between the three patient groups in arteriolar wall area/circumference ratio (Figure 7).

Figure 7

Cardiomyocyte width (A), capillary length density (B), diffusion radius (C), and arteriolar wall area/circumference ratio (D) in left ventricular biopsies from control (Con), metabolic syndrome (MetS), and type 2 diabetic (Diab) men undergoing coronary artery bypass graft surgery. Arteriolar wall area/circumference ratio was determined for arterioles with diameter (average of maximum and minimum diameter of each arteriole) of 20-80 μm. Data shown as means ± SEM.

Immunostaining for CML and RAGE

As previously described [33], immunostaining for CML was predominantly localized to the media and intima of arterioles and venules (Figure 8) and we found no difference in CML expression between the three patient groups (Figure 9). RAGE immunostaining was predominantly localized to the intima of arterioles and venules and to capillaries (Figure 10) and we found no difference in RAGE expression between the three patient groups (Figure 9).

Figure 8

Immunostaining for Nε-(carboxymethyl)lysine (CML) (A) and negative control section without primary antibody (B), of left ventricular biopsy from control coronary artery bypass graft surgery patient.

Figure 9

N. Data shown as means ± SEM.

Figure 10

Immunostaining for the receptor for advanced glycation end-products (RAGE) (A) and negative control section without primary antibody (B), of left ventricular biopsy from control coronary artery bypass graft surgery patient.

Correlations with duration of diabetes, glycemic control, and insulin resistance

Although the duration of diabetes ranged from 0-30 years, none of the parameters of myocardial structure, microvasculature, and AGE and RAGE expression correlated with diabetes duration in the diabetic subjects. By contrast, diabetes duration correlated with the E/E' ratio (r = 0.87, P = 0.03), with a weaker non-significant correlation with mitral septal E' (r = 0.83, P = 0.08).

Among all patients combined, fasting plasma glucose was positively correlated with the E/E' ratio (r = 0.46, P = 0.02), with a weaker non-significant inverse correlation with mitral septal E' (r = 0.40, P = 0.07), but was not correlated with any of the parameters of myocardial structure, microvasculature, or AGE and RAGE expression. Additionally, neither fasting plasma insulin concentrations nor HOMA2-IR was correlated with any parameter of myocardial structure, microvasculature, or AGE and RAGE expression.

Discussion

This study investigated the association of type 2 diabetes and the MetS with myocardial fibrosis (assessed by picrosirius red staining and immunostaining for collagen I and III), cardiomyocyte size, capillary length density, diffusion radius, arteriolar dimensions, and myocardial expression of CML and RAGE. We confirmed the impaired diastolic function of type 2 diabetic and MetS patients [2,34], as shown by their increased pulmonary capillary wedge pressure and reduced mitral septal E'. Our data demonstrate that the impaired diastolic function of type 2 diabetic and MetS patients was not dependent on increased myocardial fibrosis, cardiomyocyte hypertrophy, alteration of the myocardial microvascular structure, or increased myocardial expression of CML or RAGE. These data suggest that the increased myocardial fibrosis and CML expression reported by previous studies of diabetic patients with heart failure [3,12,21,22,33] were a consequence, rather than an initiating cause, of impaired cardiac function.

Our findings for myocardial fibrosis and CML expression are in agreement with a recent study by van Heerebeek et al. [22] who studied endomyocardial LV biopsies from patients hospitalized with worsening heart failure. They found no increase in fibrosis or CML expression in LV biopsies of diabetic subjects with normal LV ejection fraction, but increased fibrosis and CML expression in patients with reduced LV ejection fraction [22]. The present study extends these findings to a much earlier stage in the evolution of diabetic cardiomyopathy by study of epicardial LV biopsies from diabetic and MetS patients with increased LV filling pressures without symptomatic heart failure. Although the diabetic patients had reduced mitral septal E', we found no differences between the three patient groups for Doppler measures of left ventricular filling or left atrial size, suggesting that the impairment of diastolic function was much less than that which occurs in heart failure with preserved ejection fraction.

Cardiomyocyte size has been reported to be increased [3,13,17], normal [19], and reduced in diabetic patients [15]. Our finding of no increase in cardiomyocyte width of diabetic and MetS patients is in agreement with reports of similar cardiac mass for diabetic and non-diabetic individuals [35], and the association between increased insulin levels and cardiac hypertrophy is largely accounted for by associations with body size [36]. Moreover, our finding of no effect of diabetes and the MetS on arteriolar dimensions is in agreement with a previous autopsy study of myocardial arteries [20]. Our failure to detect hypertrophy of myocardial arterioles similar to that reported for small arteries in subcutaneous tissue of patients with type 2 diabetes [37] may be because the arterioles examined in our study were much smaller in size, and it is also possible that the effects of diabetes on vascular hypertrophy are different for different vascular beds. The similar capillary length density and arteriolar dimensions of diabetic and non-diabetic patients in this study is in agreement with the similar myocardial perfusion of diabetic and non-diabetic subjects in the fasting state [38,39], although it does not exclude an effect of diabetes and the MetS on microvascular function.

Our finding that RAGE expression was predominantly localized to vascular endothelium and capillaries is in agreement with previous studies [40], although, to our knowledge, this is the first comparison of myocardial RAGE expression in control, diabetic, and MetS patients. Whereas cell-surface-bound RAGE plays an essential role in mediating the effects of AGEs, soluble RAGE may act as an AGE inhibitor, by preventing the binding of AGEs to the cell-surface-bound RAGE receptor [41]. Our finding of similar circulating levels of soluble RAGE and cardiac expression of RAGE suggest RAGE did not participate in the impaired diastolic function of diabetic and MetS patients in our study. The similar plasma CML and LMWF levels of diabetic patients to those of control patients is in agreement with our previous study [42], and likely reflects their well-controlled diabetes.

Differences between human and animal models of diabetes

Our study highlights possible differences between diabetic humans and animal models of diabetes. In addition to the lack of increased myocardial fibrosis, we found no evidence for the cardiomyocyte and arteriolar hypertrophy and reduced myocardial capillary density reported in animal models of diabetes [7,9-11], which may be related to poorer diabetic control in animal models.

Alternative mechanisms of impaired diastolic function of diabetes and the MetS

Many mechanisms other than increased fibrosis, cardiomyocyte hypertrophy and alteration in myocardial vasculature have been proposed to explain the diastolic dysfunction of diabetes and the MetS. These include alterations in cardiomyocyte metabolism, abnormal calcium homeostasis and contractile mechanisms, oxidative stress, direct glucotoxicity, and inflammation [1,2,5,8,22,43,44]. Our data are compatible with a role for both insulin resistance and hyperglycemia in the pathogenesis of the diastolic dysfunction of diabetes and the MetS [2].

Limitations

Our study had a number of limitations. These included a limited sample size because of the need for myocardial biopsies from each patient. However, in a separate study of 11 control, 7 diabetic, and 6 MetS patients with aortic stenosis we similarly found no association of diabetes or the MetS with increased myocardial fibrosis or altered cardiomyocyte width, capillary length density, diffusion radius, or arteriolar dimensions, although, in comparison with the patients in this study, aortic stenosis patients had more interstitial fibrosis, greater cardiomyocyte width, lower capillary length density, and greater diffusion radius (unpublished data). Another limitation was the inherent selection bias caused by the sampling of patients presenting for coronary artery bypass graft surgery. However, in a comparison of aortic stenosis patients with and without coronary artery disease we found no effect of coronary artery disease on myocardial fibrosis, cardiomyocyte width, capillary length density, diffusion radius, or arteriolar dimensions (unpublished data). Patients with coronary artery disease were an important patient group to study because of the high prevalence of coronary artery disease in diabetic patients [45,46], and coronary artery disease patients with diabetes are twice as likely as those without diabetes to develop heart failure [6]. Although the frequent use of antihypertensive therapy, including inhibitors of the renin angiotensin system and statin therapy, may have attenuated the effect of MetS and diabetes on the myocardium, the MetS and diabetic patients in this study had evidence of diastolic dysfunction. Moreover, diabetes remains a predictor of heart failure when these therapies are included in multivariate analysis [6]. To avoid the effect of coronary stenoses on myocardial structure and the microvasculature we took particular care to collect biopsies from the same epicardial region of the LV myocardium without evidence of ischemia or wall motion abnormality, which was proximal to significant flow-limiting coronary stenoses and collaterals. However, we do not know if the data obtained apply to other regions of the myocardium, such as myocardium distal to significant flow-limiting coronary stenoses. It is also unknown whether our findings are relevant to the right ventricle, which may also contribute to diabetic cardiomyopathy [47]. Moreover, the generalizability of our findings is limited by the exclusion of women. Although we had echocardiographic data for only a limited number of patients we had hemodynamic data, including ventriculograms and pulmonary capillary wedge pressures, which provided a direct measure of LV filling pressure, for all patients.

Conclusions

We compared MetS (pre-diabetic) and diabetic patients with patients without these conditions in order to examine the effects of the insulin-resistant state before diabetes (and anti-diabetes medication) commenced, and the effects of diabetes before heart failure developed. We found that the increased LV filling pressures of MetS and type 2 diabetic patients were not dependent on increased myocardial fibrosis or alteration in cardiomyocyte size, capillary length density, diffusion radius, arteriolar dimensions, or myocardial expression of CML and RAGE. Our findings suggest that the increased myocardial fibrosis and CML expression, cardiomyocyte hypertrophy, and altered microvasculature structure previously described in diabetic heart disease were a consequence, rather than an initiating cause, of cardiac dysfunction.

Abbreviations

AGEs: advanced glycation end-products; ANOVA: analysis of variance; ARB: angiotensin receptor blocker; CML: Nε-(carboxymethyl)lysine; eGFR: estimated glomerular filtration rate calculated using the Modification of Diet in Renal Disease study equation; HOMA: Homeostasis Model Assessment calculator version 2.2; LMWF: low molecular weight fluorophore; LV: left ventricle; MetS: metabolic syndrome; NT-proBNP: amino-terminal-pro-B-type natriuretic peptide; RAGE: receptor for AGEs.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

DJC, JBS, AJJ, DLP, MY, JFK, AEN, CGS, MJB, and DJK participated in the design of the study and acquisition of the data. DJC, JBS, DLP, MJB, and DJK participated in the analysis and interpretation of data. DJC participated in manuscript preparation. JBS, AJJ, DLP, MY, JFK, AEN, CGS, MJB, and DJK participated in review of the manuscript. All authors have read and approved the final manuscript.