Association of inflammatory markers and poor outcome in diabetic patients presenting with ST segment elevation myocardial infarction.

OBJECTIVE: Carbohydrate metabolism disorders (CMD) significantly impact the development and progression of all forms of ischemic heart disease, and inflammation is regarded as a general pathogenetic link between CMD and ischemic heart disease.
METHODS: A total of 601 patients with ST segment elevation myocardial infarction (MI) (STEMI), admitted within 24 hours from the onset of symptoms during 1 year, were included in this registry study. The blood levels of inflammation markers were measured at days 10-14 with further follow up at 1 year.
RESULTS: The analysis of acute-phase percutaneous coronary intervention impact on the 1-year outcomes showed that endovascular revascularization significantly improved the 1-year prognosis of STEMI patients both with and without CMD. The analysis of inflammation markers showed significantly higher levels of interleukin (IL)-6 and sCD40L in MI patients with diabetes mellitus, and impaired glucose tolerance. Additionally, the patients with impaired glucose tolerance had significantly higher IL-12 levels. In the diabetic MI patients, the odds ratio of a poor 1-year outcome was high for patients with a high Killip classification of acute heart failure upon admission.
CONCLUSION: Persistent inflammation in STEMI patients with CMD undergoing percutaneous coronary intervention might be responsible for vascular complications within 1 year after MI. Comorbid diabetes mellitus or impaired glucose tolerance can amplify the significance of the inflammatory response for the development of adverse 1-year outcomes.

Background

Carbohydrate metabolism disorders (CMD) are thought, not only to contribute to the development of all forms of ischemic heart disease (IHD) but also, to significantly impact the prognosis.1 According to some authors, hospital and posthospital mortality in myocardial infarction (MI) patients is significantly higher if they have diabetes mellitus (DM),2,3 despite contemporary treatment modalities aimed at coronary flow restoration.

Revascularization procedures in acute MI can help optimize the prognosis in this patient category.4,5 However, a history of DM remains a risk factor for adverse cardiovascular events after primary percutaneous coronary intervention (PCI), despite encouraging results.6 Moreover, data have demonstrated a negative impact from impaired glucose tolerance (IGT) on the prognosis of MI patients, which is comparable with that of DM.7,8

Inflammation is regarded as a general pathogenetic link between CMD and IHD. Indeed, recent data have demonstrated that the increase in the levels of a range of nonspecific markers is associated with a higher risk of IHD and a poor outcome if the disease is already established.9 In an earlier manuscript published by the authors, high levels of some inflammation markers were demonstrated to be characteristic of, not only diabetic MI patients but also, those with IGT. This finding suggests that inflammation might be the leading mechanism responsible for the development of adverse cardiovascular events in both symptomatic and asymptomatic patients with CMD.10 However, the most significant inflammation markers to assess risk in MI patients with CMD undergoing PCI remain disputable. This study aimed to assess the significance of nonspecific inflammation markers to assess the risk for a poor 1-year outcome in patients with ST segment elevation MI (STEMI) and type 2 DM or IGT undergoing PCI.

Methods

The study protocol was approved by the local ethics committee of the Federal State Budgetary Institution Research Institute for Complex Issues of Cardiovascular Diseases, of the Siberian Branch of the Russian Academy of Medical Sciences and was developed according to the World Medical Association Declaration of Helsinki Ethical Principles for Medical Research Involving Human Subjects (2008 edition),11 and the “Good Clinical Practice Principles in the Russian Federation” approved by the Russian Ministry of Health Order. All patients signed an informed consent before taking part in the study.

The inclusion criterion was STEMI within 24 hours from the onset, with no age restrictions. The exclusion criteria were: MI occurring during PCI or coronary artery bypass surgery; end-stage renal failure; known cancer; worsening of any chronic disease; or any other disease that significantly limited the life expectancy.

Patient population

A total of 601 STEMI patients admitted over 1 year, within 24 hours from the onset of symptoms, were included into this registry study. The mean age was 62.90 (32.0–94.0) years. The medical history and clinical data as well as the main characteristics of the MI index and hospital treatment are summarized in Table 1.

Table 1

Clinical and medical history data of the STEMI patients (n=601)

Parameters
Female sex, n (%)	226 (37.61)
Age, years	62.90 (61.99; 63.81)
Smoking, n (%)	241 (40.09)
Arterial hypertension, n (%)	537 (89.35)
Diabetes mellitus, n (%)	140 (23.29)
Impaired glucose tolerance, n (%)	32 (5.32)
History of myocardial infarction, n (%)	166 (27.62)
History of angina pectoris, n (%)	354 (58.90)
History of stroke, n (%)	64 (10.64)
Obesity (BMI >25 kg/m2), n (%)	427 (71.04)
Left ventricular ejection fraction, %	48.97 (48.11; 49.84)
LV dysfunction (LVEF <46%), n (%)	161 (26.78)
Killip class upon admission (II–IV), n (%)	123 (20.46)
Mean TIMI score	3.94 (3.71; 4.16)
Coronary angiography, n (%)	436 (72.54)
Reperfusion, n (%)
Stenting	301 (50.08)
Balloon angioplasty	75 (12.47)
Intracoronary TLT	14 (2.32)
Hospital medications, n (%)
Antiplatelets	567 (94.34)
β-blockers	509 (84.69)
ACE inhibitors	510 (84.85)
Diuretics	240 (39.93)
Statins	152 (25.29)
Calcium channel blockers	395 (65.72)

Notes: The values given in the brackets are the median (Q1;Q3).

Abbreviations: ACE, angiotensin-converting-enzyme inhibitor; BMI, body mass index; LV, left ventricular; LVEF, left ventricular ejection fraction; STEMI, ST segment elevationmyocardialinfarction; TIMI, Thrombolysis in Myocardial Infarction; TLT, thrombolytic therapy.

Glucose tolerance test

All patients had their blood glucose levels assessed upon admission. At days 8–14, the patients with no known CMD and fasting or postprandial glucose levels of <11.1 mmol/L were subjected to an oral glucose tolerance test (OGTT) (the World Health Organization recommendation12 is for a 75 g of glucose oral dose in all adults. The dose should be drunk within 5 minutes).

A diagnosis of DM was documented if it was present in the patients’ medical records.12 New-onset type 2 DM was diagnosed during the hospital stay, based on the repeat glucose test results and OGTT findings; IGT was diagnosed during the hospital stay, based on the OGTT results.8

The diagnosis of diabetes was based on two or more independent determinations (on different days) of the glucose level that were ≥7.0 mmol/L (126 mg/dL). In doubtful cases, such as the presentation of characteristic clinical picture of diabetes with fasting plasma glucose within 6.6–7.7 mmol/L, OGTT was performed; patients with OGTT ≥11.1 mmol/L were diagnosed with type 2 DM. In addition, type 2 DM was raised when glycated hemoglobin (HbA1c) ≥6.5% (according to the recommendations of American Diabetes Association).12

Therapy

In the hospital, the patients received the therapy recommended by the 2007 National Society of Cardiology (VNOK) guidelines13 on STEMI diagnosis and treatment. The reperfusion strategy was determined as soon as possible for all patients, including: balloon angioplasty; stenting of the infarct-related artery; or intracoronary thrombolytic therapy (TLT). Systemic TLT was performed if emergency coronary angiography was contraindicated. The main contraindication for TLT was late admission (more than 12 hours from the disease onset), and PCI was contraindicated if diffuse coronary lesions were present and the infarct-related artery could not be determined.

The total extent of coronary artery disease was assessed by the Syntax score14 while considering the lesion location and a range of morphologic characteristics (occlusion, bifurcation, ostial stenosis, prolonged lesion, calcinosis, intracoronary thrombosis, etc)15 using the online calculator.16

In this study, coronary angiography was performed in 436 (72.55%) STEMI patients. Based on the obtained data, 373 (62.06%) patients underwent primary PCI for the index MI (Table 1), and a noninvasive treatment strategy was chosen for 228 (37.94%) patients. Out of 373 patients that underwent successful PCI, stents were implanted in 301 (80.70%) patients; 14 (3.75%) and 75 (20.10%) patients had intracoronary thrombolysis and balloon angioplasty (percutaneous transluminal coronary angioplasty) performed, respectively.

A total of 59 (9.81%) patients died during the hospital stay; all deaths were due to MI complications (heart ruptures, cardiogenic shock, or lung edema). In all, 15 (25.42%) deceased patients were diabetic, and two (3.38%) individuals had IGT.

During the hospital stay, all patients were administered combined coronaroactive and antithrombotic therapy (anticoagulants, antiplatelet agents, beta-blockers, angiotensin-converting-enzyme inhibitor (ACE) inhibitors, statins, and calcium channel blockers) according to individual indications. All patients with documented CMD received medical counseling about lifestyle modifications, including sufficient physical exercise (depending on the time from MI onset), diet, and body weight reduction; if indicated, glucose-lowering medications (biguanides) were recommended, and the insulin dose was adjusted, if necessary.

The 1-year outcome was assessed in 470 (86.72%) patients; a total 72 (13.28%) patients were lost to follow up. In all, 155 (32.98%) end points, including 59 (12.55%) deaths, 86 (18.30%) recurrent MIs, 52 (11.06%) cases of unstable angina, 18 (3.83%) strokes, 20 (4.26%) hospital admissions for heart failure, and 40 (8.51%) emergency PCIs were registered during the study. The causes of deaths during hospital stay were early complications of MI - cardiorrhexis, pulmonary edema, and cardiogenic shock. During the year, the fatality in 56 (94.92%) cases had cardiovascular causes - development of reinfarction, augmentation of chronic heart failure (pulmonary edema), stoke development, and ventricular arrhythmias. In other cases, fatality occurred in two (3.39%) patients with oncopathology and in one (1.69%) patient, as a result of a road traffic accident.

Assays

Blood serum and plasma were tested. The serum was separated from venous blood by centrifugation at 3,000× g for 20 minutes and stored at −70°C. The blood levels of inflammation markers (fibrinogen, interleukin [IL]-6, IL-8, IL-12, tumor necrosis factor [TNF]-α, high-sensitivity C-reactive protein [hsCRP], and sCD40L) were measured at days 10–14, with further follow up at year 1, to determine the clinical significance of inflammation markers in predicting cardiovascular events after PCI. Cytokine Quantikine® (R&D Systems, Inc., Minneapolis, MN, USA) tests were used for: human IL-6 (sensitivity =0.16 ng/mL; intra- and interassay precision, coefficients of variation [CV] =5.7 and 8.2%), human IL-8 (sensitivity =0.011 ng/mL, intra- and interassay precision; CV =4.4 and 7.3%), human IL-12 (sensitivity =0.011 ng/mL, intra- and interassay precision; CV =4.4 and 7.3%), human TNF-α (sensitivity =9.0 pg/mL, intra- and interassay precision; CV =4.5 and 7.0%), and sCD40L (sensitivity =0.12 ng/mL, intra- and interassay precision; CV =6.4 and 11.4%). hsCRP was analyzed by means of solid-phase enzyme immunoassay (EIA), using a BioMedica kit (Waterloo, NSW, Australia) (sensitivity =0.12 ng/mL, intra- and interassay precision; CV =6.1 and 9.4%). The risk of death or myocardial infarction in patients assessed by TIMI Risk Score.17

Statistical analysis

The data were statistically processed using SPSS Statistics for Windows, Version 21.0 (IBM Corp, Armonk, NY, USA) software. The Shapiro-Wilk test was used to assess the normality of continuous data. Most of the data had statistically significant deviations from the normal distribution; therefore, Me (Q1;Q3) was used where Me was the median, and 25%–75% was the interquartile range that comprised 50% of the data on both sides of the median. The nonparametric Mann–Whitney U-test was used to test the hypothesized differences between the samples. The differences between the categorical variables in the mismatched samples were analyzed using χ2 test, with Yates’ correction for continuity. The frequency of the properties in the groups was analyzed by means of the odds ratio calculation. P<0.05 was considered statistically significant.

Results

With regard to the presence of CMD, STEMI patients were divided into three groups: normal blood glucose (n=429 [71.38%]); IGT (n=32 [5.33%]); and DM (n=140 [23.29%]), of which 16 (11.42%) had new-onset DM.

The analysis of medical history and clinical characteristics of STEMI patients with regard to CMD showed that the “most severe” group included diabetic patients, while the “least severe” group included those with normal blood glucose levels, and IGT patients comprised a “borderline” group (Table 2). Diabetic patients more often had arterial hypertension, a history of MI, angina pectoris, and congestive heart failure (CHF); these patients also more often had high Thrombolysis in Myocardial Infarction (TIMI) scores, were admitted to the hospital for CHF, had Killip III or IV scores,18 and had higher rates of rethrombosis during their hospital stay. The IGT group, compared with the diabetic patients and those with normal blood glucose levels, more often included obese patients and those with a history of CHF and stroke. Additionally, the groups of STEMI patients with DM and IGT included more women than did the group comprised of patients with normal blood glucose levels.

Table 2

Clinical and medical history data of the STEMI patients with regard to carbohydrate metabolism disorders

Parameters	Normal glucosea (n=429)	DMb (n=140)	IGTc (n=32)	P-value
Mean age, years	61.0 (53.0; 72.0)	66.0 (58.0; 71.0)	59.5 (54.0; 69.0)	P=0.106a,bP=0.304a,cP=0.027b,c
Female sex, n (%)	123 (28.67)	86 (61.42)	17 (53.12)	P≤0.001a,bP=0.007a,cP=0.506b,c
Arterial hypertension, n (%)	375 (87.41)	133 (95.0)	29 (90.62)	P=0.018a,bP=0.592a,cP=0.799b,c
Obesity, n (%)	282 (65.73)	116 (87.22)	29 (90.62)	P≤0.001a,bP=0.027a,cP=0.819b,c
History of MI, n (%)	104 (24.24)	52 (37.14)	10 (31.25)	P=0.004a,bP=0.500a,cP=0.6732,3
History of angina pectoris, n (%)	229 (53.37)	103 (73.57)	22 (68.75)	P≤0.001a,bP=0.134a,cP=0.740b,c
History of CHF, n (%)	27 (6.29%)	14 (10.0%)	3 (9.37%)	P=0.027a,bP=0.673a,cP=0.506b,c
History of stroke, n (%)	36 (8.39)	21 (15.0)	7 (21.87)	P=0.036a,bP=0.027a,cP=0.493b,c
Smoking, n (%)	188 (43.82)	31 (22.14)	22 (68.75)	P≤0.001a,bP=0.011a,cP≤0.001b,c
LVEF, %	50.0 (43.0–56.0)	49.0 (44.0–55.0)	48.50 (40.0–55.50)	P=0.535a,bP=0.734a,cP=0.983b,c
LV dysfunction (LVEF <46%), n (%)	136 (31.70)	41 (29.29)	10 (31.25)	P=0.666a,bP=0.960a,cP=0.996b,c
MI localization, n (%)
Anterior MI	205 (47.79)	70 (50.0)	19 (59.38)	P=0.006a,b
Posterior MI	200 (46.62)	55 (39.29)	13 (40.62)	P=0.416a,c
Posterior MI with the right	10 (2.33)	1 (0.71)	0 (0)	P=0.274b,c
ventricle affected
Circular MI	14 (3.26)	414 (10.0)	0 (0)
Killip class upon admission, n (%)
I	331 (77.16)	90 (64.29)	20 (62.50)	P≤0.001a,b
II	70 (16.32)	22 (15.71)	10 (31.25)	P=0.109a,c
III	16 (3.73)	21 (15.0)	2 (6.25)	P=0.090b,c
IV	12 (2.79)	7 (5.0)	0 (0)
Mean TIMI score	3.0 (2.0; 6.0)	4.0 (2.0; 6.0)	3.5 (2.0; 6.0)	P=0.184a,bP=0.934a,cP=0.857b,c
SYNTAX	17.65 (15.34; 20.05)	21.04 (17.56; 23.78)	18.22 (15.82; 22.15)	P=0.262a,bP=0.653a,cP=0.506b,c

Notes:

group with normal glucose.

group with diabetes mellitus.

group with impaired glucose tolerance.

Abbreviations: CHF, congestive heart failure; DM, diabetes mellitus; IGT, impaired glucose tolerance; LV, left ventricular; LVEF, left ventricular ejection fraction; MI, myocardial infarction; STEMI, ST segment elevation myocardial infarction; TIMI, Thrombolysis in Myocardial Infarction.

MI patients with DM and IGT had a more extensive coronary artery disease (Syntax score) compared with the patients with normal blood glucose, who also had severe coronary lesions; however, these differences were not statistically significant (Table 2).

Coronary angiography only or PCI did not result in statistically significant differences (Table 3).

Table 3

Main characteristics of hospital coronary interventions for the STEMI patients with regard to carbohydrate metabolism disorders

Parameters	Normal glucosea (n=429)	DMb (n=140)	IGTc (n=32)	P-value
Coronary angiography, n (%)	309 (72.03)	104 (74.29)	23 (71.87)	P=0.681a,bP=0.960a,cP=0.955b,c
PCI, n (%)	274 (63.87)	79 (56.43)	20 (62.50)	P=0.140a,bP=0.960a,cP=0.668b,c
Stenting, n (%)	219 (51.05)	66 (47.14)	16 (50.0)	P=0.481a,bP=0.960a,cP=0.924b,c
Balloon angioplasty, n (%)	58 (13.52)	12 (8.57)	5 (15.62)	P=0.162a,bP=0.946a,cP=0.380b,c
TLT, n (%)
Systemic	35 (8.16)	11 (7.86)	3 (9.38)	P=0.729a,b
Intracoronary	11 (2.56)	2 (1.43)	1 (3.12)	P=0.951a,cP=0.766b,c

Notes:

group with normal glucose.

group with diabetes mellitus.

group with impaired glucose tolerance.

Abbreviations: DM, diabetes mellitus; IGT, impaired glucose tolerance; PCI, percutaneous coronary intervention; STEMI, ST segment elevation myocardial infarction; TLT, thrombolytic therapy.

During the hospital stay, the diabetic STEMI patients more often developed early postinfarction angina, rethrombosis, and recurrent MI compared with the patients with normal blood glucose (Table 4). Similar to the diabetic patients, IGT patients also had higher rates of early postinfarction angina and recurrent MI compared with those who had normal blood glucose.

Table 4

Hospital outcome of the STEMI patients with regard to carbohydrate metabolism disorders

Parameters	Normal glucosea (n=429)	DMb (n=140)	IGTc (n=32)	P-value
Composite hospital end points, n (%)	81 (18.88)	36 (25.71)	7 (21.87)	P=0.106a,bP=0.855a,cP=0.821b,c
Hospital death, n (%)	42 (9.79)	15 (10.71)	2 (6.25)	P=0.878a,bP=0.730a,cP=0.663b,c
Restenosis/rethrombosis, n (%)	15 (3.50)	16 (11.43)	2 (6.25)	P=0.001a,bP=0.756a,cP=0.587b,c
Early postinfarction angina, n (%)	23 (5.36)	15 (10.71)	3 (9.37)	P=0.045a,bP=0.581 a,cP=0.960b,c
Recurrent in-hospital MI, n (%)	26 (6.06)	19 (13.57)	4 (12.50)	P=0.007a,bP=0.292a,cP=0.960b,c
Stroke, n (%)	1 (0.23)	0 (0)	0 (0)	P=0.960a,bP=0.960a,cP=0.960b,c

Notes:

group with normal glucose.

group with diabetes mellitus.

group with impaired glucose tolerance.

Abbreviations: DM, diabetes mellitus; IGT, impaired glucose tolerance; MI, myocardial infarction; STEMI, ST segment elevation myocardial infarction.

The analysis of 1-year outcomes showed that the diabetic patients had 1.5-fold more end points (P=0.005) than did patients with normal blood glucose and 1.3-fold more end points than did the IGT patients (Table 5). Despite the lack of differences in the rate of end points between the MI patients with IGT and those with normal blood glucose, the IGT group had the highest admission rates for unstable angina and more often underwent emergency revascularization within 1 year. Thus, the presence of DM and IGT in MI patients determines a more complicated course of index MI.

Table 5

End points within 1 year after STEMI with regard to carbohydrate metabolism disorders (n=470)

End points	Normal glucosea (n=429)	DMb (n=140)	IGTc (n=32)	P-value
Composite end point, n (%)	92 (28.84)	52 (43.70)	11 (36.67)	P=0.005a,bP=0.491a,cP=0.624b,c
Death, n (%)	39 (12.22)	18 (15.12)	2 (6.67)	P=0.520a,bP=0.544a,cP=0.360b,c
MI, n (%)	49 (15.36)	31 (26.05)	6 (20.0)	P=0.015a,bP=0.686a,cP=0.653b,c
Stroke, n (%)	8 (2.50)	9 (7.56)	1 (3.33)	P=0.031a,bP=0.960a,cP=0.675b,c
Unstable angina, n (%)	29 (9.09)	18 (15.13)	5 (16.67)	P=0.101a,bP=0.310a,cP=0.960b,c
CHF worsening, n (%)	10 (3.14)	9 (7.56)	1 (3.33)	P=0.078a,bP=0.960a,cP=0.675b,c
Emergency PCI, n (%)	18 (5.64)	16 (13.45)	6 (20.0)	P=0.012a,bP=0.009a,cP=0.538b,c

Notes:

group with normal glucose.

group with diabetes mellitus.

group with impaired glucose tolerance.

Abbreviations: CHF, congestive heart failure; DM, diabetes mellitus; IGT, impaired glucose tolerance; MI, myocardial infarction; PCI, percutaneous coronary intervention; STEMI, ST segment elevation myocardial infarction.

The analysis of the impact of acute-phase PCI on 1-year outcomes showed that endovascular revascularization significantly improved the 1-year prognosis of STEMI patients, both with and without CMD (Table 6). The benefits of a restored coronary flow were especially evident in STEMI patients with DM or IGT. CMD patients had significantly less adverse events within a year after the index MI compared with those with normal blood glucose. In this regard, the progression of the IGT postinfarction was similar to that of the diabetic patients.

Table 6

One-year outcome in the groups with regard to PCI and IGT

1-year outcomes	No PCI		PCI		P-value
	Carbohydrate metabolism disorders	Normal blood glucose	Carbohydrate metabolism disorders	Normal blood glucose
Good outcome, %	51.56	54.26	63.22	78.22	≤0.001*≤0.001**
Poor outcome, %	48.44	45.74	36.78	21.28	≥0.05

Notes:

significant differences between normal blood glucose (PCI) and carbohydrate metabolism disorders (PCI).

Significant differences between normal blood glucose (no PCI) and normal blood glucose (PCI).

Abbreviations: IGT, impaired glucose tolerance; PCI, percutaneous coronary intervention.

Thus, the study results demonstrate that both DM and IGT in MI patients equally determine, not only a more complicated course of the disease but also, a poor 1-year outcome. Moreover, PCI in STEMI patients with DM or IGT represents a significant prognostic benefit in terms of the reduction of adverse events within 1 year.

The analysis of inflammation markers showed significantly higher levels of IL-6 and sCD40L in the MI patients with DM and IGT. Additionally, the IGT patients had significantly higher IL-12 levels compared with the patients with normal blood glucose (Table 7).

Table 7

Inflammation markers in STEMI patients with regard to carbohydrate metabolism disorders

Inflammation markers	Normal glucosea (n=429)	DMb (n=140)	IGTc (n=32)	P-value
Fibrinogen, g/L	3.2 (2.58; 4.2)	3.75 (2.84; 6.05)	3.5 (2.34; 5.08)	P=0.005a,bP=0.493a,cP=0.308b,c
TNF-α, pg/mL	9.61 (7.24; 11.99)	9.32 (6.16; 13.68)	9.75 (7.05; 12.79)	P=0.871a,bP=0.534a,cP=0.727b,c
IL-10, pg/mL	1.78 (1.06; 2.72)	2.13 (1.22; 3.31)	1.98 (1.15; 3.05)	P=0.528a,bP=0.204a,cP=0.215b,c
IL-8, pg/mL	3.35 (1.65; 5.73)	3.24 (1.88; 5.84)	3.53 (1.74; 5.96)	P=0.810a,bP=0.450a,cP=0.376b,c
IL-6, pg/mL	2.05 (0.44; 5.68)	4.75 (0.79; 7.46)	3.97 (0.56; 6.49)	P=0.023a,bP=0.039a,cP=0.278b,c
IL-12, pg/mL	99.0 (64.07; 120.3)	109.50 (95.63; 128.0)	122.5 (107.30; 133.50)	P=0.152a,bP=0.017a,cP=0.032b,c
CRP, mg/L	11.95 (6.57; 19.75)	13.10 (5.52; 18.0)	12.03 (5.47; 17.56)	P=0.687a,bP=0.785a,cP=0.432b,c
sCD40l, ng/mL	4.85 (2.16; 8.42)	8.30 (5.77; 10.44)	7.87 (3.55; 9.79)	P=0.031a,bP=0.045a,cP=0.308b,c

Notes: Values are presented as median (Q1:Q3).

group with normal glucose.

group with diabetes mellitus.

group with impaired glucose tolerance.

Abbreviations: CRP, c-reactive protein; DM, diabetes mellitus; IGT, impaired glucose tolerance; IL, interleukin; sCD40L, CD40 ligand; STEMI, ST segment elevation myocardial infarction; TNF, tumor necrosis factor; Q, interquartile range.

The odds ratios (OR) were calculated to determine the factors that implicate a poor 1-year failure, including, left ventricular (LV) dysfunction, high levels of inflammation markers (TNF-α, IL-12, and IL-6) at days 10–14 from MI onset, admission glucose levels of >7.8 mmol/L, and recurrent in-hospital MI.

In the diabetic MI patients, the OR of a poor 1-year outcome was high for patients with a high Killip class of acute heart failure upon admission, a history of chronic heart failure, LV dysfunction, and high IL-12 levels. In the IGT group, the factors associated with adverse outcomes were a history of angina pectoris, admission glucose levels of >7.8 mmol/L, and high IL-12 levels (Table 8). Prognostically unfavorable levels of inflammation markers and glucose were calculated, along with the most optimal sensitivity and specificity.

Table 8

Factors associated with poor 1-year outcome

Parameters	Odds ratio	95% CI	P-value
Normal glucose
Female-to-male ratio	1.97	1.17–3.31	0.008
Ratio of the patients older and younger than 70 years	3.77	2.24–6.35	<0.0001
History of MI	1.86	1.08–3.22	0.020
History of angina pectoris	2.02	1.23–3.32	0.007
History of stroke	2.67	1.11–6.39	0.009
LVEF <46%	3.81	2.26–6.45	<0.0001
Ratio of Killip II–IV and I	3.21	1.81–5.71	<0.0001
Admission glucose of >7.8 mmol/L	3.51	2.11–5.83	<0.0001
PCI	0.33	0.20–0.55	<0.0001
Recurrent in-hospital MI	3.20	0.84–7.21	0.029
TNF-α >14.12 pg/mL	4.73	1.93–11.58	0.0001
IL-6 >8.05 pg/mL	3.14	1.29–7.67	0.007
IL-12 >110.01 pg/mL	5.18	1.54–7.37	0.009
Diabetes mellitus
History of chronic heart failure	3.71	0.67–8.40	0.039
LVEF <46%	4.01	1.35–8.37	0.034
Ratio of Killip II–IV and I	3.51	1.31–7.05	0.041
PCI	0.23	0.15–0.69	0.039
IL-12 >110.01 pg/mL	5.57	1.01–9.34	0.033
Impaired glucose tolerance
History of angina pectoris	1.37	0.61–3.09	0.044
PCI	0.20	0.10–0.63	0.022
Admission glucose of >7.8 mmol/L	1.93	0.43–8.61	0.038
IL-12 >110.01 pg/mL	4.74	1.12–6.17	0.024

Abbreviations: CI, confidence interval; IL, interleukin; LVEF, left ventricular ejection fraction; MI, myocardial infarction; PCI, percutaneous coronary intervention; TNF, tumor necrosis factor.

For all STEMI patients, the OR of a poor 1-year outcome was significant if PCI was not performed. The OR method was also used to compare the efficacy of endovascular revascularization in the study groups. To this end, the STEMI patients that underwent PCI were considered to be the exposed subgroup, and the controlled event – the incidence of which depended on the exposing factor – was the occurrence of end points within the 1-year follow-up period. The data presented in this study showed that revascularization procedures in the acute MI phase helped to optimize the 1-year outcome in all of the three patient groups (OR =0.33, P<0.0001 [normal blood glucose group]; OR =0.23, P=0.039 [DM group]; and OR =0.20, P=0.022 [IGT group]). However, the efficacy of PCI was much higher in both the ITG and in the DM groups than in the normal blood glucose patients.

Discussion

First, DM MI patients were more effectively treated than were those with normal blood glucose. This effect was likely due to the higher absolute risk for cardiovascular events in DM MI patients, which results in a higher therapeutic benefit.19

However, the negative impact of DM on the outcomes of MI patients should also be considered when PCI is performed, which has also been demonstrated in this manuscript.5 Indeed, despite encouraging results, a history of DM remains a risk factor for early and late events after primary PCI.6 DM patients have been proven to have a high risk of restenosis and repeat revascularization.20 DM patients have higher rates of atherosclerosis progression both in revascularized and nonrevascularized areas.21

In a previous study, we obtained data that confirmed a negative impact of IGT on MI prognosis similar to that of DM.7 Diabetic patients with chronic hyperglycemia and dyslipidemia typically have signs of active intravascular inflammation is a prerequisite for higher rates of atherosclerosis progression in addition to increased platelet activity, which is also typical of diabetic patients.22 These relationships should be considered when discussing the mechanisms of a favorable prognosis in patients with IGT.

In a previous work, the authors demonstrated that both MI patients with DM and those with IGT have a high proinflammatory potential, which is manifested in the increased levels of CRP, IL-12, and sCD40L. Therefore, inflammation can be regarded as the leading mechanism of the manifestation of adverse vascular events in patients with both symptomatic and subclinical IGT.10

In the current study IL-12 played an important role in the risk assessment of adverse events in both CMD and normal glucose patients. The function of IL-12 as an inflammation marker in atherosclerosis is unclear, and most relevant studies have been experimental. IL-12 and IL-18 have been established as powerful inducers of interferon gamma (IFN-γ) production,23 a proinflammatory cytokine that accelerates atherosclerosis progression.24 This cytokine produced by macrophages was found to cause undifferentiated CD4+ cells to differentiate into T helper (Th) 1 cells, which help define the cells responsible for specific immune system response by means of IL-2, IFN-γ, TNF-α, and the CD 40 ligand.25

A previous immunohistochemical study showed increased IL-12 levels in human atherosclerotic plaques compared with normal arteries.26 Another study demonstrated the role of IL-12 in murine atherosclerosis development and progression.27 In an earlier study the authors found that IL-12 also played a very important role in predicting vascular events in STEMI patients within the 1-year follow-up period.28 This marker remained important to predict the outcomes after MI, both in the patients with and without a history of CMD in this study. Thus, IL-12 might be an independent marker of atherosclerosis progression.

Another cytokine examined in this study, IL-6, could discriminate patients at a high risk for new vascular accidents within 1 year after MI treated with an invasive approach. The prognostic value of IL-6 has been demonstrated in population epidemiology studies.29,30 In one study, increased IL-1 and IL-6 were confirmed to be associated with recurrent coronary events in IHD patients.31 Martins et al showed significant increases in IL-2, IL-4, IL-6, IL-12, and IL-18 in IHD patients compared with healthy subjects, and the levels of IL-6 were much higher in MI patients.32 Kubensky et al33 assessed the concentrations of inflammation markers in patients with Q-wave MI, at days 2–10: higher IL-6 and TNF-α levels were observed if the MI course was complicated. Kopitsa34 showed that IL-6 >180 pg/mL at days 4–6 from the acute MI onset was a highly sensitive but less specific marker for recurrent coronary events and sudden coronary death in this category of patients. Meanwhile, Orlova35 demonstrated that only extremely low admission IL-6 levels were predictors of hospital mortality in patients with acute Q-wave MI compared with the other inflammation markers under study (CRP, IL-6, IL-8, IL-12, and IL-10).

Previously published data support the association between the increase in TNF-α and recurrent coronary events in IHD patients.36 The Cholesterol and Recurrent Events (CARE) study demonstrated that increased expression of TNF-α 9 months after MI was a predictor of high risk of coronary events within a 5-year follow-up period.37 The results of this study showed the role of this marker in the prediction of adverse outcomes in MI patients who underwent PCI. The latest studies have found that TNF-α and IL-6 produced in the adipose tissue could influence the peripheral tissue sensitivity to insulin.38,39

Studying the role of proinflammatory cytokines (TNF-α, IL-6, and CRP) and their impact on the vascular complications of DM has suggested that inflammation plays a specific role in the development of insulin resistance. Chronic subclinical inflammation is thought to be a part of insulin resistance syndrome, and the aforementioned cytokines are predictors of vascular DM complications.38,39 Hyperglycemia was confirmed to be one of the main stimuli for the expression of inflammation markers by endothelial cells.40 Convincing experimental and clinical study has confirmed the role of hyperglycemia in the increase in CRP, IL-6, and TNF-α levels.40 Additionally, hyperglycemia enhances the release of reactive oxygen, which can cause a more severe oxidative stress than chronic hyperglycemia, if glucose levels change dramatically.41

The results of this study showed the role of inflammation as a general pathogenetic link in atherogenesis, atherothrombosis (MI), and CMD development, which confirmed the association between these conditions and the need for proinflammatory status assessment to stratify the risk of MI patients. Thus, persistent inflammation in STEMI patients with CMD undergoing PCI might be responsible for vascular accidents within 1 year after MI. Comorbid DM or IGT can amplify the significance of the inflammatory response for the development of adverse 1-year outcomes.