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Archives of Medical Science : AMS logoLink to Archives of Medical Science : AMS
. 2017 Jan 19;13(2):311–320. doi: 10.5114/aoms.2017.65240

Biochemical markers of type 2 diabetes as a late complication of myocardial infarction: a case-control study

Olga Barbarash 1, Olga Gruzdeva 1, Evgenya Uchasova 1,, Ekaterina Belik 1, Yulia Dyleva 1, Victoria Karetnikova 1
PMCID: PMC5332457  PMID: 28261283

Abstract

Introduction

On average, 19–23% of patients with acute myocardial infarction (MI) suffer from type 2 diabetes mellitus, which is newly diagnosed in a significant number of patients. Both classic carbohydrate metabolism and lipid metabolism may be promising diagnostic markers for insulin resistance in acute coronary syndrome.

Material and methods

Two hundred patients (130 males and 70 females aged 61.4 ±1.12 years) with ST-segment elevation MI were included in the study. Patients were divided into two groups based on manifestations of diabetes: (1) 171 patients without diabetes within 1 year after MI; and (2) 29 patients with manifestations of diabetes. The control group comprised 33 people without diseases of the cardiovascular system and diabetes and was matched by age and gender with patients.

Results

In patients with an imbalanced adipokine state during the acute phase of MI, we noted an increased concentration of free fatty acids (p > 0.05) and reduced ghrelin levels (p > 0.05) and activation of the proinflammatory and thrombotic potentials of blood plasma. Patients who developed diabetes 1 year after MI showed hospital stays with more pronounced changes in the study parameters.

Conclusions

The most informative biochemical parameters associated with the development of diabetes at 1 year after MI were adiponectin, retinol protein, ghrelin, tumor necrosis factor α, and plasminogen activator inhibitor.

Keywords: type 2 diabetes mellitus, adipokines, ghrelin, tumor necrosis factor α, myocardial infarction

Introduction

Acute coronary syndrome (ACS) continues to be associated with a high incidence of in-hospital and post-hospital discharge complications [1]. On average, 19–23% of patients with acute myocardial infarction (MI) suffer from type 2 diabetes mellitus, which is newly diagnosed in a significant number of patients [2, 3]. The percentage of ACS patients with previously and newly diagnosed diabetes is 45–53%, and the percentage with impaired glucose tolerance is 20–36% [3]. An increased risk of death for diabetic patients with acute MI may persist for several years.

Both classic carbohydrate metabolism (hyperglycemia and hyperinsulinemia) and lipid metabolism may be regarded as promising diagnostic markers for insulin resistance in ACS. Lipid metabolism disorders are considered major risk factors for the development and progression of cardiovascular disease [4, 5]. Among lipid metabolism parameters in ACS, the most significant forms are those that involve cholesterol transport and free fatty acids (FFA), which provide up to 70% of the energy requirements for myocardium and reflect typical pathological patterns occurring in the ischemic/necrotic area and, therefore, are associated with functional impairment of cardiac muscle [6]. The importance of studying FFA is because of their participation in the development of insulin resistance [7, 8], hyperglycemia, diabetes manifestation (in which endothelial dysfunction results in macro- and microangiopathy), impairment of cardiovascular activity, and the initiation of early and late cardiovascular complications in MI [6, 8].

Besides the classical parameters of carbohydrate metabolism that are considered diagnostic markers of insulin resistance, lipid metabolism parameters and their regulators should also be included, these being adipokines, inflammation and thrombogenesis [911]. The investigation of possible pathogenic associations between the studied parameters may be important for understanding the fundamental mechanisms and manifestations of diabetes, and may be a theoretical basis for risk stratification of ACS complications and improvement of quality of life in patients with previous MI. This study aimed to identify the most significant parameters of carbohydrate and lipid metabolism, adipokines and proinflammatory and prothrombogenic states associated with the development of diabetes 1 year after MI.

Material and methods

Two hundred patients (130 males and 70 females aged 61.4 ±1.12 years) with ST-segment elevation MI were included in the study. Patients were divided into groups based on the manifestation of diabetes in the late MI period: group 1 (n = 171) without diabetes in the late MI period; and group 2 (n = 29) with diabetic manifestations 1 year after MI. The control group included 33 participants without cardiovascular diseases and diabetes and was comparable in age and gender to the enrolled patients (Table I).

Table I.

Initial clinical and anamnestic characteristics of patients

Variable Patients without type 2 diabetes (n = 171) Patients with first diagnosed type 2 diabetes (n = 29) P-value
Men, n (%) 107 (63.0) 23 (79.0) 0.20
Age [years] 62.58 ±1.2 59.5 ±2.2 0.30
Clinical measures:
 Body mass index [kg/m2] 25.5 29.02 0.04
 Overweight, n (%) 129 (75.6) 23 (79.0) 0.29
 Arterial hypertension, n (%) 126 (74.0) 24 (84.2) 0.05
 Current smoking, n (%) 123 (71.8) 18 (63.2) 0.22
 Family history of IHD, n (%) 41 (23.7) 20 (68.4) 0.03
 Family history of T2DM, n (%) 5 (2.9) 7 (24.1) 0.01
 Clinic angina to myocardial infarction, n (%) 91 (53.0) 15 (52.6) 0.32
 Previous myocardial infarction, n (%) 47 (27.6) 12 (42.1) 0.12
 Cerebrovascular accident/transient ischemic attack in history, n (%) 9 (5.5) 2 (5.2) 0.36
 A history of heart failure, n (%) 60 (35.4) 6 (21.0) 0.37
Depth of lesion:
 Q-wave MI 119 (69.6) 24 (84.2) 0.04
Non-Q-wave MI 52 (30.4) 5 (15.8) 0.05
Localization of MI:
 Posterior 62 (35.61) 12 (42.1) 0.12
 Posterior taking the right ventricle front 11 (6.50) 2 (5.2) 0.36
 Front 98 (55.8) 15 (52.6) 0.12
Acute heart failure (Killip):
 I 143 (83.9) 17 (57.9) 0.043
 II 18 (10.4) 7 (26.3) 0.036
 III 7 (3.3) 5 (15.8) 0.022
 IV 3 (2.2) 0
Rhythm disturbance, n (%) 86 (50.2) 15 (52.6) 0.231
Early post-infarction angina, n (%) 10 (6.1) 7 (26.3) 0.023
Recurrent MI (for the period of stay in hospital), n (%) 7 (4.4) 5 (15.8) 0.031

The study protocol was approved by the local ethics committee of the Federal State Budgetary Scientific Institution Research Institute for Complex Issues of Cardiovascular Diseases, developed in accordance with the WMA Declaration of Helsinki “Ethical principles for medical research involving human subjects” (amended in 2000) and “Rules for clinical practice in the Russian Federation”, approved by the Ministry of Health of the Russian Federation in 19 June 2003. All patients provided written informed consent to participate in the study.

Inclusion criteria were acute ST-segment elevation MI, confirmed according to the principles of the All-Russian Scientific Society of Cardiology (2007), and admitted to the hospital within 24 h after the onset of symptoms. Exclusion criteria were previously or newly diagnosed type 2 diabetes at the time of the index event, severe diseases affecting prognosis (anemia, renal and hepatic failure, cancer, acute infectious and inflammatory diseases), autoimmune diseases, long-term corticosteroid therapy and death during either the in-hospital or the post-hospital (within 12 months) period. A limitation of the study was the lack of measurement of uric acid levels and parameters of physical activity.

All patients in the absence of contraindications during the in-hospital period received combined coronaroactive, antithrombotic and lipid-lowering therapy, including aspirin, clopidogrel, β-blockers, angiotensin convertase enzyme (ACE) inhibitors, statins and antiangina medications in accordance with standard clinical practice. Reperfusion therapy included primary percutaneous coronary intervention of the infarct-dependent artery, performed in 181 (90.5%) patients, and systemic thrombolysis with streptokinase 1.5 MIU in 12 (6%) patients.

Adverse outcomes after MI included reinfarction, worsened angina, decompensated heart failure and requirement of hospitalization within the 1-year follow-up.

A structured mathematical model was used to assess insulin resistance levels at days 1 and 12 based on fasting plasma insulin and glucose values and by calculating the QUICKI (Quantitative Insulin Sensitivity Check Index) [11] according to the following formula: QUICKI = 1/[log (I0) + log (G0)], where I0 is basal insulinemia (mMU/ml), and G0 is basal glycemia (mg/dl). Katz et al. reported that an average QUICKI value of 0.382 + 0.007 corresponds to normal tissue sensitivity to insulin; and a QUICKI value of 0.331 + 0.010 and 0.304 + 0.007 correspond to moderate and severe tissue insulin resistance, respectively [12].

An oral glucose tolerance test (OGTT) was performed to verify diabetes during the in-hospital period (on day 12) and 1 year after MI according to the algorithms of specialized medical care [9]. Fasting glycemia was measured in patients after 3 days of an unrestricted diet, with the last uptake being 30–50 g of carbohydrates. Plasma glucose was determined 2 h after administration of a 75-g glucose-containing solution, consumed over 3–5 min. Patients were not allowed to smoke during OGTT. Postprandial glycemia was measured when the fasting glycemia level was ≥ 7.8 mmol/l (2 h after a meal containing 20–24 g of carbohydrates, 6.9 g of protein and 8.11 g of fat). Diagnostic criteria for diabetes according to WHO recommendations (1999–2006) were fasting venous plasma glucose ≥ 7.0 mmol/l or 2 h after OGTT/postprandial ≥ 11.1 mmol/l glycated hemoglobin (HbA1c) level ≥ 6.5% [9].

Assays

Blood serum and plasma were tested. Serum was separated from venous blood by centrifugation at 3000 × g for 20 min and stored at –70°C. FFA, total cholesterol (TC), triacylglycerols (TAG), low-density lipoprotein (LDL-C), very-low-density lipoprotein (VLDL-C), apolipoprotein B (apo B), high-density lipoprotein (HDL-C) and apolipoprotein A1 (apo A1) levels were measured at the same time points using a standard Thermo Fisher Scientific test system (Thermo Fisher Scientific Oy, Vantaa, Finland) in a Konelab 30i biochemistry analyzer (Thermo Fisher Scientific Oy).

The intra-assay coefficients of variation (CV) for insulin Diagnostic Systems Laboratories and C-peptide ELISA were 3.8 and 4.2%, respectively, and the inter-assay CV were 6.9 and 7.9%, respectively.

Adipokines (leptin, adiponectin, resistin and retinol-binding protein (RBP)) and ghrelin levels were measured with the BioVendor R&D Product (Brno, Czech Republic) and intra-assay CV values were 5.9 and 6.8%. Proinflammatory factors (interleukin-6 (IL-6) and tumor necrosis factor α (TNF-α)) were assessed using standard test kits (Bender MedSystems GmbH, Vienna, Austria) (CV, 7.03–8.99%), C-reactive protein (CRP) (Biomerica, Irvine, CA, USA) (CV, 2.3-4.1%) and plasminogen activator inhibitor (PAI-1) (Technoclone GmbH, Vienna, Austria) (CV, 4.03–6.39%).

Statistical analysis

Statistical analysis was performed using Statistica 6.1. software (InstallShield Software Corp., Chicago, IL, USA) and SPSS 10.0 for Windows (SPSS Inc., Chicago, IL, USA). Results are presented as median (Me) and 25 and 75% quartiles Me (Q1; Q3). Nonparametric tests were used to assess and analyze data. The Mann-Whitney U test or the Kolmogorov-Smirnov method (more than 50 cases in each group) were used for quantitative comparisons of two independent groups. The Spearman rank correlation coefficient was used to investigate relationships between variables. Stepwise logistic regression analysis with odds ratios (OR) and 95% confidence intervals (CI) were used to determine the prognostic significance of parameters in long-term prognosis. Cox regression was used to evaluate the risk of unfavorable events; the impact of independent variables, predictors of risk, was determined. A p-value of < 0.05 was considered statistically significant.

Results

One year after MI, type 2 diabetes was verified in 29 (14.5%) patients. Five patients were diagnosed with the disease after 7 months following a visit to the endocrinologist, 18 patients were diagnosed after 9 months after MI during routine clinical examinations, and 6 patients were diagnosed during a follow-up visit to the center after 12 months.

The OGTT defined impaired carbohydrate tolerance in patients with newly diagnosed type 2 diabetes in acute MI (Table II). There was a 1.6-fold increase of postprandial glucose levels, a 1.4-fold increase of insulin and a 1.9-fold increase of C-peptide compared with healthy control subjects, and a 1.2-fold, 1.4-fold and 1.7-fold increase, respectively, compared with non-diabetic patients.

Table II.

Basal and postprandial levels at 1 and 12 days after MI development

Variable Control (n = 33) Patients without type 2 diabetes (n = 171) Patients with first diagnosed type 2 diabetes (n = 29)
Basal level Postprandial level 1st day 12th day 1st day 12th day
Basal level Postprandial level Basal level Postprandial level
Glucose [mmol/l] 4.40 (3.60; 5.50) 4.38 (3.40; 5.80) 6.20 (5.51; 8.10)a 5.60 (5.01; 6.20)b 5.80 (4.91; 6.80) 6.70 (5.81; 8.10)a 6.00 (4.80; 7.01) 6.70 (5.81; 8.11)c
Insulin [mU/ml] 12.50 (8.70; 18.50) 28.12 (4.80; 43.20) 12.71 (2.51; 19.80) 12.52 (2.61; 15.23) 26.72 (2.37; 41.01) 14.11 (8.61; 21.0) 15.32 (10.52; 22.50) 38.55 (4.72; 63.60)a,c,d
C-peptide [ng/ml] 1.20 (0.73; 1.87) 1.78 (0.73; 1.98) 1.03 (0.35; 1.79) 1.01 (0.50; 1.41) 2.43 (0.81; 3.43) 1.01 (0.68; 1.46) 1.75 (0.72; 1.95)b,c 3.51 (1.06; 6.74)a,d
a

Compared with the control group (p < 0.05)

b

statistically significant differences in parameters at day 1 and day 12 (p < 0.05)

c

reliable differences between groups at day 1 (p < 0.05)

d

statistically significant differences between groups at day 12 (p < 0.05).

The manifestation of diabetes in examined patients was associated with the progression of impaired insulin resistance, diagnosed during the in-hospital period of MI. Analysis of insulin resistance using QUICKI estimated in the acute phase of MI showed significant differences between the diabetic and non-diabetic patients. The QUICKI was 0.293 ±0.012 in patients with newly diagnosed diabetes, and corresponded to remarkable tissue-specific insulin resistance. One year later the QUICKI decreased to 0.280 ±0.014 (p = 0.004). In patients without diabetes, the QUICKI corresponded to moderate insulin resistance, both in the acute phase and 1 year after MI. For both groups of patients the QUICKI values were lower than that observed for the control group (0.380 ±0.010).

The development of diabetes in the post-hospital period was facilitated by cardiovascular risk factors and a history of diabetes in patients with MI. All patients with diabetes, verified 1 year after MI, were overweight and hypertensive and had a genetic burden for coronary heart disease and diabetes.

Initiation of diabetes over the longer term was preceded by a more severe course of the disease during the in-hospital period; Q-wave MI prevailed in diabetic patients as well as signs of congestive heart failure Killip class II–IV. Common in-hospital complications of MI included early post-infarction angina and recurrent MI (Table III).

Table III.

Adverse outcomes observed in MI patients with and without diabetes at 1 year after MI

Endpoints Patients without type 2 diabetes (n = 171) Patients with first diagnosed type 2 diabetes (n = 29) P-value
Unstable angina 31 (18.1%) 9 (31%) 0.008
Reinfarction 19 (11%) 6 (21%) 0.003
Decompensation of chronic heart failure 35 (20.46%) 11(37.93%) 0.002

P-value for differences between groups.

The post-hospital period of MI in patients with diabetes was also defined by a more severe course. Diabetic patients with MI had a higher incidence of unstable angina, reinfarction and decompensated heart failure, requiring hospitalization (Table III). There were therefore no differences in therapies during the post-hospital period. All patients received antiplatelet (95% and 80.9%, p = 0.23), coronaroactive (98% and 96%, p = 0.46) and hypolipidemic (89% and 75%, p = 0.75) therapies at almost the same frequency.

Logistic regression analysis allowed for the identification of factors associated with the manifestation of diabetes within 1 year after MI (Table IV). The most statistically significant parameters were severity of congestive heart failure and infarct size (Table V). In all derived anthropometric indices, an increased body mass index (BMI) had a close relationship with diabetes development. However, the presence of insulin resistance during the in-hospital period significantly contributed to the manifestation of diabetes and resulted in a 4-fold increased risk for developing type 2 diabetes 1 year after MI (Table V).

Table IV.

Biochemical maker data for the development of diabetes at 1 year after MI

Variable 1st day 12th day
OR 95% CI AUN P-value OR 95% CI AUN P-value
Glucose [mmol/l] 1.07 1.05–1.95 0.62 0.01 2.99 1.77–5.95 0.87 0.03
Insulin [mU/ml] 1.08 1.01–1.17 0.74 0.04 2.99 1.01–1.47 0.83 0.04
C-peptide [ng/ml] 1.98 1.03–1.22 0.58 0.33 1.52 1.08–1.07 0.79 0.02
TC [mmol/l] 1.14 1.01–1.02 0.51 0.41 0.93 0.99–1.05 0.47 0.64
TAG [mmol/l] 1.82 0.77–1.89 0.65 < 0.001 1.22 1.11–1.35 0.58 0.04
HDL-C [mmol/l] 0.87 0.98–1.04 0.42 0.86 0.42 0.99–1.00 0.48 0.22
LDL-C [mmol/l] 0.99 0.47–3.60 0.47 0.96 0.51 0.80–1.23 0.34 0.02
VLDL-C [mmol/l] 3.74 0.59–1.64 0.65 < 0.001 2.18 1.09–1.51 0.58 0.04
apo B [g/l] 1.20 0.17–4.40 0.61 0.43 0.82 0.61–1.60 0.52 0.54
apo A1 [g/l] 1.05 0.96–1.04 0.48 0.96 0.80 0.83–1.57 0.49 0.60
apo B/apo A1 0.98 1.52–9.21 0.65 0.90 1.83 0.17–6.49 0.51 0.06

P-value compared with the control group. TC – total cholesterol, TAG – triglyceride, HDL-C – high-density lipoprotein cholesterol, LDL-C – low-density lipoprotein cholesterol, VLDL-C – very-low-density lipoprotein cholesterol, apo B – apolipoprotein B, apo A1 – apolipoprotein A1.

Table V.

Clinical data of the development of diabetes at 1 year after MI

Variable OR 95% CI AUC P-value
Age [years] 0.99 0.74–3.57 0.46 0.77
Killip 1.63 1.01–1.81 0.53 0.02
Number of affected arteries 1.38 0.91–3.67 0.59 0.18
Ejection fraction 1.01 0.99–1.14 0.52 0.81
Body mass index 1.10 1.21–2.74 0.61 0.03
Myocardial infarct size 1.2 1.04–2.1 0.5 0.02
Percutaneous coronary intervention 0.26 0.1–0.9 0.75 0.04
Insulin resistance 4.17 1.12–15.58 0.91 0.03

P-value compared with the control group. OR – odds ratio, 95% CI – 95% confidence interval, AUC – area under the ROC curve.

The most informative markers of diabetes among carbohydrate metabolism parameters were glucose, insulin and C-peptide, measured on day 12 of MI. Elevated levels of glucose and insulin provoked a 3-fold increase of insulin resistance risk and a 1.5-fold increase of C-peptide.

Besides carbohydrate metabolism disorders, lipid metabolism disorders were detected. Patients with newly diagnosed diabetes reported elevated levels of TAG, VLDL-C, and apo B/apo A ratio and low levels of HDLC compared with non-diabetic patients and the control group (Table VI). The greatest changes were observed in FFA levels, with diabetic patients showing a 9-fold increase in FFA and patients without diabetes showing a 8.2-fold increase on day 1 compared with the control group (Table VI). By day 12, patients in both groups showed decreased FFA levels, but levels remained 3.5-fold higher than the control group.

Table VI.

Lipid profiles for patients with MI in the dynamics of hospital stay (Me: Q1; Q3)

Variable Control (n = 33) Patients without type 2 diabetes (n = 171) Patients with first diagnosed type 2 diabetes (n = 29)
1st day 12th day 1st day 12th day
TC [mmol/l] 4.30 (3.50; 6.10) 5.55 (4.40; 6.50)a 5.40 (4.40; 6.40) 5.50 (4.20; 7.00)a 5.70 (4.90; 6.10)
TAG [mmol/l] 1.13 (0.78; 1.23) 1.60 (1.15; 2.17) 2.05 (1.43; 2.70)b 2.75 (2.01; 2.87)a,c 2.57 (1.44; 3.22)
HDL-C [mmol/l] 1.31 (1.02; 1.72) 1.02 (0.83; 1.16) 1.02 (0.84; 1.16) 0.78 (0.58; 0.94)a,c 0.84 (0.58; 1.13)
LDL-C [mmol/l] 2.03 (1.51; 2.55) 2.74 (2.09; 3.41) 2.62 (1.95; 3.35) 1.98 (1.86; 3.10) 2.41 (0.82; 2.56)
VLDL-C [mmol/l] 0.44 (0.33; 0.53) 0.73 (0.52; 0.98) 0.93 (0.65; 1.23)b 1.25 (0.91; 1.30)a,c 1.17 (0.65; 1.46)
apo B [g/l] 1.02 (0.76; 1.25) 1.18 (0.95; 1.39) 1.36 (1.08; 1.64) b 1.51 (1.19; 1.72)a 1.38 (1.21; 1.84)
apo A1 [g/l] 1.43 (1.29; 1.73) 1.27 (1.11; 1.42) 1.38 (1.18; 1.74)b 1.13 (1.06; 1.22)a 1.15 (1.01; 1.63)
apo B/apo A1 0.71 (0.59; 1.00) 0.90 (0.75; 1.12) 0.92 (0.73; 1.16) 1.25 (1.12; 1.62)a,c 1.05 (0.83; 1.60)
FFA [μmol/l] 0.20 (0.10; 1.10) 1.63 (1.24; 2.00)a 0.54 (0.41; 0.73)b 1.91 (1.62; 2.05)a 0.90 (0.59; 0.99)b,c
a

Statistically significant difference compared with the control group (p < 0.05)

b

reliable differences in indicators at day 1 and day 12 (p < 0.05)

c

reliable differences between parameters of the study groups (p < 0.05). TC – total cholesterol, TAG – triglyceride, HDL-C – high-density lipoprotein cholesterol, LDL-C – low-density lipoprotein cholesterol, VLDL-C – very-low-density lipoprotein cholesterol, apo B – apolipoprotein B, apo A1 – apolipoprotein A1.

For parameters of lipid metabolism, FFA levels were independently associated with insulin resistance development in MI. Elevated FFA levels on day 1 at 1 mmol/l increased 1.8-fold the risk of insulin resistance development, and on day 12 increased 2-fold. While increased TAG and VLDL-C levels had statistically significant associations with the manifestation of diabetes, they did not have high diagnostic specificity or sensitivity; the area under the curve (AUC) was 0.65, corresponding to an unsatisfactory quality of the model (Table IV).

Assessment of adipokine status showed a reduction of ghrelin as well as low activation of proinflammatory and thrombotic potentials of blood plasma. A 2.05-fold increase in leptin levels, a 4.56-fold increase in RBP and an 8.15-fold increase in FFA levels were determined on day 1 of MI, whereas the antidiabetic protective factor ghrelin decreased 3.24-fold compared with the control group (Table VII). IL-6, CRP, TNF-α and PAI-1 increased at 3.78-, 22.96-, 11.66- and 2.43-fold, respectively, compared with the control group.

Table VII.

Adipokine, prothrombogenic and proinflammatory levels in patients at 1 and 12 days after MI (Me: Q1; Q3)

Variable Control (n = 33) Patients without type 2 diabetes (n = 171) Patients with first diagnosed type 2 diabetes (n = 29)
1st day 12th day 1st day 12th day
Leptin [ng/ml] 6.98 (4.5; 9.75) 14.34 (9.54; 27.67)a 10.13 (8.43; 22.80)b 26.29 (20.45; 29.31)a,c 18.69 (14.86; 27.30)b,d
Resistin [ng/ml] 7.0 (3.8; 9.8) 8.67 (4.60; 10.78) 8.60 (4.60; 10.50) 16.66 (9.98; 18.22)a,c 11.76 (9.89; 17.38)a,b,d
Retinol-binding protein [μg/ml] 47.5 (20.0; 76.7) 216.95 (185.20; 246.25)a 185.88 (194.23; 248.75)a,b 299.85 (212.60; 278.90)a,c 243.35 (184.20; 245.10)a,b,d
Adiponectin [mg/ml] 11.35 (7.3; 13.5) 11.20 (9.00; 15.20) 11.45 (8.63; 15.00) 8.10 (6.50; 8.50)a,c 8.50 (7.90; 13.80)a,c
Ghrelin [ng/ml] 55.2 (31.6; 90.2) 17.06 (14.80; 17.67)a 16.86 (13.12; 18.20)a 13.81 (11.21; 18.27)a,c 12.86 (11.12; 18.20)a,d
Interleukin-6 [pg/ml] 3.90 (2.80; 4.10) 14.78 (9.02; 21.64)a 7.76 (2.7; 12.19)b 25.92 (14.45; 38.03)a,c 11.24 (9.36; 14.94)b,d
C-reactive protein [mg/l] 1.15 (0.86; 2.10) 26.41 (14.00; 40.80)a 11.87 (5.00; 20.47)b 45.00 (15.97; 60.00)a,c 25.0 (6.00; 37.21)b,d
Tumor necrosis factor-α [pg/ml] 1.20 (0.90; 2.10) 14.00 (12.87; 22.86)a 19.80 (11.84; 23.25)b 24.80 (21.64; 23.50)a,c 32.76 (21.56; 44.57)b,d
Plasminogen activator inhibitor-1 [ng/ml] 35.25 (28.30; 46.30) 85.80 (37.24; 131.00)a 62.34 (37.24; 102.10)b 143.70 (137.00; 183.10)a,c 145.30 (85.79; 202.50)d
a

Compared with the control group (p < 0.05)

b

statistically significant differences in parameters at day 1 and day 12 (p < 0.05)

c

statistically significant differences between groups at day 1 (p < 0.05)

d

statistically significant differences between groups at day 12 (p < 0.05).

Patients with verified diabetes 1 year after MI showed more pronounced changes in the studied parameters during the in-hospital period. On day 1 of MI, the levels of diabetes-related adipokines (leptin, resistin, RBP) and FFA were 1.83-, 1.92-, 1.38- and 1.17-fold higher compared with non-diabetic patients (Table VII). Ghrelin and adiponectin levels in patients with diabetes decreased 1.4- and 4-fold compared with the control group, and 1.18- and 1.23-fold compared with diabetic patients. Concentrations of IL-6, TNF-α and PAI-1 increased 1.7-fold compared with non-diabetic patients (Table VII).

On day 12 of MI, patients without diabetes showed a 1.4-fold decrease in leptin, a 1.17-fold decrease in RBP and a 3-fold decrease in FFA. Resistin and adiponectin levels were within the range of the control group, but ghrelin deficiency remained (Table VII).

A similar pattern was observed for proinflammatory and prothrombogenic factors: levels of IL-6 decreased 1.9-fold, CRP decreased 2.2-fold, and PAI-1 decreased 1.37-fold compared with day 1. The exception was TNF-α levels, which increased by 41%.

Patients with diabetes manifestation had pronounced changes on day 12 of the hospital stay. Leptin, resistin, RBP and FFA showed 1.8-, 1.4-, 1.3- and 1.6-fold increases, respectively, compared with patients without diabetes (Table VII). The concentrations of adiponectin and ghrelin decreased 1.35- and 1.31-fold compared with non-diabetic patients.

Levels of proinflammatory factors (IL-6 and CRP) on day 12 decreased 2.3- and 1.8-fold compared with day 1, but remained 1.4- and 2.1-fold higher than levels in patients without diabetes. There was no essential dynamics of PAI-1. The TNF-α levels increased 32% and exceeded 1.65-fold the values of the non-diabetic group.

Although adipokines (resistin and leptin) and the proinflammatory factor CRP showed statistically significant differences, these markers did not show high diagnostic sensitivity or specificity, which represented an AUC value equal to 0.6, corresponding to a low quality of the model (Table VIII).

Table VIII.

Data for the development of diabetes at 1 year after MI

Variable 1st day 12th day
OR 95% CI P-value AUN OR 95% CI P-value AUN
Leptin [ng/ml] 1.02 1.01–1.09 0.25 0.55 1.02 1.01–1.06 0.36 0.54
Resistin [ng/ml] 1.06 0.99–1.12 0.12 0.63 1.12 1.00–1.02 0.01 0.78
Adiponectin [mg/ml] 0.41 0.39–1.02 0.01 0.84 0.53 0.49–1.44 0.04 0.83
Retinol-binding protein [μg/ml] 1.61 0.95–1.22 0.03 0.86 1.99 0.93–1.35 0.03 0.89
Ghrelin [ng/ml] 0.19 0.85–2.70 0.03 0.93 0.22 0.93–1.03 0.04 0.94
Interleukin-6 [pg/ml] 1.35 1.06–4.49 0.02 0.79 1.42 0.35–1.84 0.03 0.78
Free fatty acids [μmol/l] 2.9 1.38–6.11 0.01 0.70 1.82 0.6–5.51 0.29 0.56
C-reactive protein [mg/l] 1.03 0.44–1.53 0.01 0.60 1.01 0.98–3.41 0.59 0.53
Tumor necrosis factor [pg/ml] 1.54 1.01–1.08 0.03 0.81 1.52 0.67–1.28 0.03 0.76
Plasminogen activator inhibitor-1 [ng/ml] 1.8 0.10–1.66 0.01 0.87 2.1 1.29–2.88 0.01 0.88

P-value compared with the control group. OR – odds ratio, 95% CI – 95% confidence interval, AUC – area under the ROC curve.

From AUC > 0.75 values, the most sensitive and specific markers were adiponectin, ghrelin, RBP, TNF-α, IL-6 and PAI-1. Low levels of adiponectin during the in-hospital period of MI increased the risk for developing diabetes by 50% and ghrelin increased the risk by 78–81% (Table VIII). Elevated levels of TNF-α, IL-6, RBP and PAI-1 increased 1.5-, 1.4-, 1.8- and 2-fold the risk for developing diabetes (Table VIII).

Discussion

Acute coronary syndrome is commonly associated with a high incidence of in-hospital and post-hospital complications. On average, 19–23% of patients with acute MI suffer from type 2 diabetes [13]. Impaired glucose tolerance is observed in a significant number of patients. This category of patients is at high risk for developing cardiovascular diseases [13, 14] and diabetes.

The results of the current study showed that 14.5% of patients at 1 year after MI suffered from type 2 diabetes. The in-hospital period of MI for these patients was characterized by severe insulin resistance. Insulin resistance transformation into diabetes in the current study may have been provoked by several pathological factors during the acute phase, these being basal and postprandial hyperglycemia, hyperinsulinemia, dyslipidemia, adipokine imbalance and activation of proinflammatory and prothrombogenic potentials. One year after MI, insulin resistance was aggravated and reached diagnostic values for diabetes and was associated with a high incidence of adverse cardiovascular events, including recurrent MI, progressive angina and decompensated heart failure.

Late diabetes manifestation was preceded by a more severe hospital period of infarction, including heart failure, recurrent ischemia and myocardial contractile dysfunction. Results from the current study are consistent with a study by Stubbs et al. [15]. In that study, the authors reported that insulin resistance was a reliable predictor of adverse cardiovascular events over the long term in patients with MI and without a history of diabetes. This predictive ability of insulin resistance remained after adjustments were made for gender, age and BMI. Of note, the authors did not find a similar pattern for patients with stable coronary artery disease.

An important factor for the manifestation of diabetes in the late MI period may be the presence of cardiovascular risk factors, including obesity, hypertension and genetic burden for diabetes, with insulin resistance being a common pathogenic link [16]. From regression analysis in the current study, the presence of insulin resistance during the in-hospital period of MI was associated with a 4-fold increased risk for developing type 2 diabetes 1 year after MI (OR = 4.17; 95% CI: 1.12–15.58). This finding is consistent with the concept of the triggering role of carbon exchange in diabetes manifestation.

The results of the current suggest that insulin resistance may not only be a response to catecholamine stress accompanying MI, but also a pathophysiological basis for metabolic and neuro-endocrine disorders contributing to adverse long-term outcomes in ACS. Insulin is known to stimulate intracellular transport of glucose, which is the preferable substrate for cardiomyocytes in ischemia/reperfusion injury. Experimental studies reported a decrease of glycogen synthesis in cardiomyocytes in insulin resistance due to impaired glucose transport into cells [17]. Recently, cardiomyocytes in patients with coronary artery disease demonstrated the same resistance to insulin, mediating glucose distribution towards glycolysis [17]. Activation of glycolysis in ischemic myocardium can be counterproductive because of the accumulation of reactive oxygen species and lactate with cytotoxic effects. Therefore, MI patients with insulin resistance may be affected not only by low glycogen in cardiomyocytes, but also further delivery of glucose to ischemic cardiomyocytes will contribute to a reduction, resulting in a cell energy deficit and subsequent decrease in functional activity.

In the current study, the in-hospital course of MI in patients with manifested diabetes was accompanied by the highest levels of blood FFA. Nolan et al. [18] suggested that under physiological conditions FFA can stimulate insulin secretion from its own receptor (FFAR1/GPR40) on β-cells as well as by intermediate metabolites (LC-CoA, DAG, PL) involved in the signaling pathways, regulating insulin secretion. However, chronic excess of FFA, apparently caused by induction of lipolysis in adipocytes and impaired FFA utilization by cardiomyocytes in myocardial ischemia with hyperglycemia, reduces biosynthesis [19] and insulin secretion [20] and induces apoptosis of β-cells [21].

Pathological activation of FFA is known to be limited by adiponectin, which blocks the synthesis of FFA and enhances FFA oxidation and increases sensitivity to insulin [22]. Decreased levels of adiponectin in the acute phase of MI may contribute to FFA lipotoxic effects, insulin resistance development and diabetes manifestation over the longer term of the disease.

The RBP had a more pronounced prognostic value compared with adiponectin, showing 1.6- and 1.99-fold increases for the risk for developing diabetes. The high diagnostic value of RBP is associated with its ability to induce enzymes of gluconeogenesis and, as a consequence, hyperglycemia. Additionally, RBP decreases insulin-stimulated glucose uptake by myocytes, inhibits the functioning of the GLUT-4 glucose transporter and inhibits insulin secretion by pancreatic β-cells [22, 23]. It is possible that leptin may contribute to increased RBP expression as its level increased 1.8-fold in patients with diabetes in the current study. Mattu and Randeva suggested leptin to have a dose-dependent effect in relation to the stimulation of the expression of RBP in adipocytes [10].

Patients with manifested diabetes 1 year after MI demonstrated more pronounced signs of nonspecific inflammation (elevated levels of IL-6, TNF-α and CRP) in the acute phase of the disease. Increases in concentrations of proinflammatory factors were accompanied by hyperglycemia and hyperinsulinemia, elevated levels of FFA and adipokines initiating insulin resistance, and deficit of the antidiabetogenic factors adiponectin and ghrelin.

In terms of physiological norms, interactions between adipokines that induce and block insulin resistance development are coordinated by proinflammatory cytokines, which also have the ability to modulate intracellular signaling of insulin [6]. Proinflammatory factors are known to induce the expression of adipokine mRNA in cardiomyocytes and adipocytes [6]. Thus, adipokines affect the synthesis of TNF-α and IL-6 by immune system cells [5]. The acute phase of MI is marked by excess expression of proinflammatory factors in the ischemic/myocardial necrotic zone and secretion into the blood, having a significant impact on adipokine imbalance. With a predominance of adipokines, tissue sensitivity to insulin is affected and contributes to hyperglycemia and diabetes within 1 year.

The association between the activation of inflammation and thrombosis, the underlying cause of atherosclerosis, and, particularly, acute MI, is established [19]. Most cases of coronary thrombosis occur as a result of destabilization of atherosclerotic plaques and are followed by release of proinflammatory cytokines into the systemic circulation, triggering a cascade of events leading to inflammation, endothelial injury and vascular thrombosis [24]. Proinflammatory cytokines activate the generation of proteins, depressing the fibrinolysis system, particularly PAI-1 [25]. In the current study, increased levels of PAI-1 were observed in both groups of patients; patients with newly diagnosed type 2 diabetes 1 year after MI showed high levels during the in-hospital period.

Correlations were observed between the concentrations of PAI-1 and IL-6 (r = 0.51, p = 0.002), and TNF-α (r = 0.47, p = 0.001) in MI patients. This supports our hypothesis, which suggests the involvement of thrombus cytokine-associated mechanisms.

Elevated PAI-1 levels may also be caused by ghrelin deficiency, which showed low concentrations especially in patients with verified diabetes 1 year after MI. It has previously been reported that PAI-1 levels negatively correlated with ghrelin levels in children with a simple type of obesity [26]. The authors suggested that suppression of ghrelin secretion may be provoked by higher insulin resistance and may be associated with visceral fat accumulation and elevated levels of PAI-1 [27]. In the current study, ghrelin was characterized by a high predictive value in relation to the development of diabetes on days 1 and 12 of MI. Ghrelin improves insulin sensitivity by activating AMP-kinase and neutralizing FFA cytotoxic effects and their metabolic intermediates.

In conclusion, adiponectin, RBP, ghrelin, TNF-α and PAI-1 appear to be the most informative biochemical parameters associated with the development of diabetes 1 year after MI. Accumulation of prothrombogenic and proinflammatory proteins, adipokines, in the peripheral circulation affects tissue sensitivity to insulin, contributing to malfunctioning of cardiomyocytes and worsened myocardial contractile function and triggering the clinical manifestations of insulin resistance in diabetes.

Acknowledgments

The authors wish to thank Olga Akbasheva for assistance in writing this article.

Conflict of interest

The authors declare no conflict of interest.

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