Cardiovascular Diabetology

, 11:93

2-h postchallenge plasma glucose predicts cardiovascular events in patients with myocardial infarction without known diabetes mellitus

Authors

    • Department of Cardiology KarolinskaUniversity Hospital, Karolinska Institute
  • Stefan Agewall
    • Department of CardiologyOslo University Hospital Ullevål, Oslo University

DOI: 10.1186/1475-2840-11-93

Abstract

Background and purpose

The incidence of cardiovascular events remains high in patients with myocardial infarction (MI) despite advances in current therapies. New and better methods for identifying patients at high risk of recurrent cardiovascular (CV) events are needed. This study aimed to analyze the predictive value of an oral glucose tolerance test (OGTT) in patients with acute myocardial infarction without known diabetes mellitus (DM).

Methods

The prospective cohort study consisted of 123 men and women aged between 31–80 years who had suffered a previous MI 3–12 months before the examinations. The exclusion criteria were known diabetes mellitus. Patients were followed up over 6.03 ± 1.36 years for CV death, recurrent MI, stroke and unstable angina pectoris. A standard OGTT was performed at baseline.

Results

2-h plasma glucose (HR, 1.27, 95% CI, 1.00 to 1.62; P < 0.05) and smoking (HR, 3.56, 95% CI, 1.02 to 12.38; P < 0.05) proved to be independent predictors of CV events in multivariate statistical analysis after adjustments for age, sex, total cholesterol, and other baseline characteristics.

Conclusions

In this study population, with previous MI and without known DM, 2-h PG and smoking were significant predictors of CV death, recurrent MI, stroke and unstable angina pectoris, independent of baseline characteristics and medical treatment.

Abbreviations

OGTT

Oral glucose Tolerance Test

CV

Cardiovascular

MI

Myocardial Infarction

DM

Diabetes Mellitus

FPG

Fasting Plasma Glucose

CAD

Coronary Artery Disease

AGEs

Advanced glycation End products

AMI

Acute Myocardial Infarction

CRF

Case Report Form

IGT

Impaired Glucose Tolerance

NGT

Normal glucose tolerance

BMI

Body Mass Index

ADA

American Diabetes Association

CHD

Coronary Heart Disease

TNF-α

Tumor Necrosis Factor alpha

PAI

Plasminogen Activator Inhibitor.

Introduction

Previous studies have shown that almost two thirds of patients with cardiovascular disease suffer from abnormal glucose metabolism [1, 2]. The majority of these cases are not detected by fasting plasma glucose (FPG) but with 2-h PG after OGTT [1, 3]. There is evidence that postprandial hyperglycemia is an independent risk factor for atherosclerosis and has an even greater effect than fasting plasma glucose [4, 5] on future events.

The pathophysiology behind the association between postprandial hyperglycemia and atherosclerosis is not fully understood. Our research group has previously reported a correlation between 2-h PG and inflammation parameters in patients with coronary artery disease (CAD) [4].

According to current understanding, hyperglycemia induces oxidative stress which, in combination with soluble advanced glycation end products (AGEs) and lipid peroxidation products leads to endothelial dysfunction and expression of inflammatory genes [68].

The purpose of this study was to analyze the predictive value of an OGTT in patients with acute myocardial infarction (AMI) without known DM after several years of follow-up.

Methods

Subjects

123 patients, men and women aged between 31–80 years with a previous acute MI, took part in the study. The inclusion criterion was hospital-diagnosed myocardial infarction that had occurred 3–12 months before the examinations. The patients were recruited from the department of Cardiology at Karolinska University Hospital Huddinge, Sweden. 90% of the participants were examined within three months of the MI. We chose three months to ensure the examination took place when patients were in a clinically stable condition. All patients who were admitted to the cardiac intensive care unit because of acute myocardial infarction were included in the study, consecutively, throughout the period 2002–2003. The exclusion criteria were known diabetes mellitus and chronic inflammatory disease. Blood samples had been taken for the control of inflammatory factors in another study. All subjects gave informed consent after written and oral information.

The Karolinska Institute ethics committee at Karolinska University Hospital Huddinge approved the study. All of the patients except five (who had moved to another city) were followed up at our outpatient clinic every six months and all CV events were recorded in a case report form (CRF). The five patients who had moved were telephoned for a clinical check-up every six months.

Acute MI was defined using the criteria of the European Society of Cardiology and the American College of Cardiology [9].

Follow-up and cardiovascular events

All patients were followed up over 6.03 ± 1.36 years. The primary end point was defined as any of the following: death from any cause, nonfatal reinfarction or stroke, unstable angina pectoris, congestive heart failure requiring hospitalization, and coronary revascularization procedure (percutaneous coronary angioplasty or coronary artery bypass grafting). Time to first event was used as the endpoint. When revascularization procedures occurred during AMI or unstable angina, it was recorded as a single event (e.g. AMI treated with primary percutaneous angioplasty was recorded as AMI. A peripheral vascular event was defined as any increase in peripheral ischemic symptoms resulting in any peripheral revascularization procedure (percutaneous transluminal angioplasty or operation). The absence of any of these features was considered as event-free survival.

Measurements

Venous blood was drawn after an overnight fast and five min of supine rest, to determine the plasma glucose and plasma levels of cholesterol and triglycerides using established methods. Plasma glucose concentrations at 0 and 120 min following ingestion of 75 g glucose were analyzed, using glucose oxidase technique on a Hitachi 917 system. DM and impaired glucose tolerance (IGT) were defined based on American Diabetes Association (ADA) definitions [10]. On the basis of 2-h PG alone, individuals were classified into categories of newly diagnosed diabetes, IGT and normal glucose tolerance (NGT) if their 2-h PG concentrations were ≥ 11.1, 7.8–11.0 and < 7.8 mmol/l, respectively.

Resting blood pressure was measured in the right arm after about 10 min of supine rest. Body mass index (BMI) was measured according to recommended principles. Smoking was assessed by a questionnaire.

Echocardiography

All patients underwent a standard echocardiographic evaluation, using a 2.5 MHz transducer (System Five, GE Vingmed, Horten, Norway). The echocardiographic studies were performed with the subject in supine left lateral decubitus, after 30 minutes of rest. One physician recorded all the echocardiograms. Two-dimensional imaging of the longitudinal parasternal view was checked in order to avoid angulation of the ultrasonic beam, and consequent changes in the left ventricular shape. Left ventricular internal dimension, left ventricular posterior wall and interventricular septum thickness were measured, according to the recommendations of the American Society of Echocardiography [11]. The ejection fraction was calculated according to Simpson’s formula.

Statistical analysis

Results are presented as means and standard deviations of the mean. All data analyses were done using Statistica for Windows software version 10.0. Mann–Whitney U test and X² test were performed. The Cox regression model was used to identify the predictive factors.

Results

Table 1 shows the baseline characteristics of the study patients. There were no significant differences between the patients with CV events compared with those without CV events regarding known risk factors such as hypertension, smoking habits, cholesterol value, LVEF and current medication. During the follow-up at 6.03 ± 1.36 years, CV events had occurred in 30 patients. Figure 1 shows the distribution of the various CV events in the patients.
Table 1

Baseline characteristics

 

Subjects with CV event n = 30

Subjects without CV event n = 93

Age (years)

62 ± 12

61 ± 10

Gender

23 (77)

71 (76)

- Male, n (%)

7 (23)

22 (24)

- Female, n (%)

  

Smoking habits

6 (20)

14 (15)

- Yes, n (%)

4 (14)

24 (26)

- Never, n (%)

19 (63)

52 (56)

- Prior smoker, n (%)

1 (3)

3 (3)

- Moist snuff, n (%)

  

BMI (kg/m2)

27 ± 4

27 ± 4

Systolic blood pressure (mmHg)

135 ± 21

138 ± 20

Diastolic blood pressure (mmHg)

77 ± 9

80 ± 9

Triglycerides, mmol/l (mean±SD)

1.7 ± 1.0

1.6 ± 1.0

Total cholesterol, mmol/l (mean±SD)

4.2 ± 0.7

4.1 ± 0.7

Heart rate, beats/min (mean±SD)

61 ± 11

58 ± 9

Fasting plasma glucose (mmol/l)

5.5 ± 1.7

5.4 ± 1.1

2-h plasma glucose (mmol/l)

8.1 ± 3.3⪵

7.5 ± 3.0

Ejection fraction (%)

49 ± 11

54 ± 7.0

*P<0.05 Mann Whitney test.

https://static-content.springer.com/image/art%3A10.1186%2F1475-2840-11-93/MediaObjects/12933_2012_Article_530_Fig1_HTML.jpg
Figure 1

Distribution of the various CV events in the patients with CV events. AP= angina pectoris, CV= cardiovascular event, MI= myocardial infarction. PCI= percutaneous coronary intervention, CABG= coronary artery bypass grafting.

Table 2 shows previous interventions and medical treatment in the study population. Coronary angiography was performed in 92 patients. That showed one vessel disease in 37 patients, two vessel diseases in 15 patients and 3 vessel diseases in 22 patients. In 16 cases no significant coronary artery stenosis was identified.
Table 2

Interventions and treatment in the study group (n=123)

Interventions

All subjects (n=123)

Subjects with CV events (n=30)

Subjects without CV events (n=93)

Previous PCI, n (%)

58 (47)

13 (43)

45 (48)

Previous CABG, n (%)

20 (16)

6 (20)

14 (15)

Thrombolysis, n (%)

18 (15)

3 (10)

15 (16)

Drugtreatment

   

Aspirin, n (%)

122 (99)

30 (100)

92 (99)

Betablocker, n (%)

111 (90)

25 (83)

86 (92)

ACE inhibitor, n (%)

31 (25)

10 (33)

21 (23)

Statin, n (%)

111 (90)

28 (93)

83 (94)

PCI= percutaneus coronary intervention. CABG= Coronary artery by-pass grafting.

ACE= angiotensin-converting enzyme. CV= Cardiovascular event.

Table 3 shows baseline characteristics of the subjects with DM, IGT and NGT. We found no statistically significant difference between the three groups with DM, IGT and NGT for the occurrence of CV events.
Table 3

Characteristics of the subjects with DM, IGT and NGT

 

DM (n = 13)

IGT (n = 29)

NGT (n = 68)

Famle

3 (23%)

6 (21%)

18 (26%)

Age (year)

61 ± 11

65 ± 8*

60 ± 12

BMI (kg/m2)

29 ± 3

27 ± 4

26 ± 3

Triglycerides (mmol/l)

2.7 ± 1.1†,§

1.8 ± 1.3

1.4 ± 0.7

Cholestrol (mmol/l)

4.9 ± 1.1

4.6 ± 0.8

4.6 ± 1.1

FPG (mmol/l)

7.7 ± 2.6†,§

5.4 ± 0.6*

4.9 ± 0.5

2-h PG (mmol/l)

14.4 ± 3.4†,§

9.2 ± 0.90*

5.8 ± 1.0

Systolic blood pressure (mmHg)

146 ± 25

146 ± 20*

133 ± 19

Diastolic blood pressure (mmHg)

79 ± 11

82 ± 10*

78 ± 9

Cardiovascular events, n(%)

3 (23)

8 (27)

19 (28)

DM, diabetes mellitus; IGT, impaired glucose tolerance; NGT, normal glucose tolerance.

† DM vs. NGT; P < 0.05.

* IGT vs. NGT; P < 0.05.

§ DM vs. IGT; p<0.05.

Table 4 shows the Cox proportional-hazards regression model with the primary end point as outcome for some important baseline variables. In this study we have only analyzed triglycerides and total cholesterol. Both these and BMI were entered in Cox proportional-hazards regression model, but they showed no significant predictive value.
Table 4

Cox proportional-hazards regressions model with primary end point as outcome, including all important baseline variables

 

Age-and gender adjusted Cox regressions

Univariate logistic regression

 

B (SE)

HR (95% CI)

P value

B (SE)

OR (95% CI)

P value

Age (years)

0.03 (0.03)

1.03 (0.96-1.10)

0.38

0.01 (0.03)

1.01 (0.96-1.07)

0.66

Systolic BP mmHg

0.02 (0.65)

1.02 (0.29-3.63)

0.98

-0.25 (0.65)

0.78 (0.22-2.78)

0.70

Fasting PG mmol/l

−0.81 (0.47)

0.44 (0.18–1.11)

0.08

-0.27 (0.37)

1.31 (0.37-1.59)

0.47

2h PG mmol/l

0.25 (0.12)

1.27 (1.00-1.62)

0.04

0.08 (0.09)

1.08 (0.91-1.29)

0.38

Smoking

1.27 (0.64)

3.56 (1.02-12.38)

0.04

1.34 (0.62)

3.83 (1.14-12.85)

0.03

Sex

0.12 (0.33)

1.27 (0.35-4.66)

0.72

0.03 (0.70)

1.03 (0.26-4.09)

0.96

BP= blood pressure, PG= plasma glucose, HR= hazard ratio, OR= odds ratio.

In multivariate statistical analysis and after adjustment for age, sex, total cholesterol, and other baseline characteristics, 2-h plasma glucose (HR, 1.27, 95% CI, 1.00 to 1.62; P < 0.05) and smoking (HR, 3.56, 95% CI, 1.02 to 12.38; P < 0.05) remained as independent predictors of CV events.

Discussion

During the six-year follow-up, the incidence of cardiovascular events after myocardial infarction was 24%. Smoking and 2-h PG were two independent predictors of CV in patients with myocardial infarction. Our research group has previously reported that the prevalence of IGT and unknown DM is high in patients with ischemic heart disease [1]. This study confirms the results from previous studies [12, 13] and highlights the clinical relevance of hyperglycemia 2-h post glucose challenge as independent risk factors for CV events in patients with ischemic heart disease. Several epidemiological studies have indicated that patients with pre-diabetic conditions, below the threshold for diabetes, are at higher risk for cardiovascular disease [14, 15]. Thus, previous studies have shown that IGT and newly detected diabetes were risk factors for increased CV events after AMI [16, 17]. However, it's still unclear whether patients with 2-h postchallenge glucose below the threshold for DM after MI are at a higher risk of CV events. This study also suggests, in line with previous reports [18, 19] that 2-h PG is a better risk predictor of CV events than FPG.

Concurring with our study, Schinner et al. [20] found a high prevalence of impaired glucose metabolism in patients with coronary heart disease (CHD) assessed by coronary angiography. They found a continuous increased risk of CHD with blood glucose levels even in the subdiabetic range. However, as in our study, they found that post-prandial hyperglycaemia contributed more to CHD than fasting hyperglycemia.

The pathophysiological mechanism behind the relationship between 2-h plasma glucose and CV events is not fully understood. Previous studies have shown that there is a correlation between 2-h plasma glucose with higher levels of plasminogen activator inhibitor (PAI) [21] and high sensitive C-reactive protein as a marker for low grade inflammation [4]. In line with our study, Chu et al. [22] showed that postchallenge hyperglycemia, increased levels of pro-inflammatory markers such as tumor necrosis factor alpha (TNF-α) and nitrotyrosone time-dependently, and that these levels were associated with coronary artery disease (CAD) in patients without previous recognized diabetes.

Disturbed glucose metabolism is associated with left ventricular dysfunction and increased intima media thickness of the carotid artery [23]. Patients with IGT often develop metabolic syndrome with increased obesity. Thus the pathophysiological relationship between 2-h plasma glucose and CV events may be explained by different mechanisms.

Other investigators have suggested age, left ventricular ejection fraction, use of beta-blockers, aspirin and statins as potential predictors for long-term CV inpatients with AMI [2427] But even after adjustment for pharmacological therapy, age and other proposed predictors, we found that 2-h post load PG and smoking were independent predictors of CV events following AMI. The observation that smoking predicts CV disease is in line with previous studies [28, 29].

Smoking is an independent risk factor for all-cause mortality and cardiovascular death and is also associated with impaired glucose tolerance and increased risk of type 2 diabetes [30, 31]. The pathophysiological mechanism by which smoking effects glucose intolerance and worsens clinical outcomes in diabetic patients is not fully understood. According to previous studies, smoking leads to increased insulin resistance, beta cell dysfunction, endothelial dysfunction and low-grade chronic inflammation [32].

Systolic blood pressure was also associated with the CV events; however, the relationship was significant only in univariate analysis. Previous studies have shown a correlation between high blood pressure and metabolic changes, such as impaired glucose tolerance and postchallenge hyperglycemia. The exact mechanism of this correlation remains somewhat unclear. It has been demonstrated that postprandial hyperglycemia is associated with increased oxidative stress [33, 34] and endothelial dysfunction [35, 36] and this would promote the development of atherosclerosis [36] and hypertension [36, 37]. Furthermore, hyperglycemia is related to decreased blood flow to skeletal muscle, resulting in decreased glucose utilization [38].

Study limitations

This study consisted of a small number of patients in a single center. Thus, despite a seemingly convincing message, our results may not reflect the real world population.

In conclusion, we show that in this study population with previous MI without known DM, 2-h plasma glucose and smoking were significant predictors of CV death, recurrent MI, stroke and unstable angina pectoris, independent of baseline characteristics and medical treatment.

Clinical implication

Our results suggest that 2-h PG and smoking could be linked to an increased risk of CV events in patients with previous MI. An OGTTcould be added to the standard risk evaluation procedures in a hospital settings, as a potential method for preventing CV events it could be the focus of future clinical investigations.

Acknowledgements

We wish to thank Magnus Backheden, Department of Learning, Informatics, Management and Ethics (LIME) for excellent support with statistic and data analysing, Margareta Berglund RN, Department of Cardiology and Karolinska University Hospital Huddinge, Karolinska Institute, Stockholm, Sweden for excellent support with recruitment of patients an data collection.

Supplementary material

12933_2012_530_MOESM1_ESM.pdf (69 kb)
Authors’ original file for figure 1

Copyright information

© Henareh and Agewall; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.