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The purpose of this study was to investigate the influence of micro- and macrovascular changes on the cardiac function in relation to left ventricular function and coronary arteries during one year in patients with type 2 diabetes.
The most frequent heart disease in patients with Type 2 Diabetes Mellitus (T2DM) is the premature development of coronary atherosclerosis, which often leads to overt ischemic heart disease (IHD). T2DM can lead to both cardiac dysfunction due to IHD or to diabetic cardiomyopathy. Diabetic cardiomyopathy is defined as an impairment of left ventricular (LV) function without overt obstructive coronary vessel disease. Diabetic cardiomyopathy has been associated with microvascular dysfunction, which leads to the inability of the heart to circulate blood effectively. The microvascular atherosclerotic changes are well known in patients with diabetes, such as impaired vision, kidney function and sensibility. The macrovascular atherosclerotic changes such as plaques in the coronary arteries are strongly associated with reduced left ventricular function.
However, the relationship between micro- and macrovascular atherosclerotic changes and the impact on cardiac function is less certain.
Estimation of cardiac function includes: Left Atrial (LA) Strain, LA Strain Rate (SR), LA Emptying Function (LAEF), LV Ejection Fraction (EF), Fractional Shortening (FS), Global Longitudinal Strain (GLS), Circumferential Strain (CS) and Radial Strain (RS), Strain Rate (SR), Peak Systolic Strain, Post Systolic Strain, Early mitral filling velocity (E), late mitral filling velocity (A), E/A ratio, Deceleration Time (DCT) of early mitral filling velocity, medial and lateral mitral velocities using tissue doppler (e' , a' and s'), E/e' ratio, Isovolumetric Relaxation Time (IVRT), Isovolumetric Closing Time (IVCT), Ejection Time (ET), Myocardial Performance Index (MPI) and Myocardial Work Index (MWI).
In this study, participants will be consisting of non-diabetic subjects and patients with diabetes type 1 + 2. All of the participants have no history of myocardial infarction, heart failure and current symptoms of cardiac disease.
The study population will undergo following examinations:
The examinations will be repeated at follow-up (however non-diabetic subjects will only have 1 CCTA performed at baseline).
The non-invasive FFR-CT will only be performed once in a subgroup of diabetic patients and non-diabetic subjects from November 2016 until May 2017.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| T2 | Patients with type 2 diabetes without myocardial infarction, heart failure and symptoms of cardiac disease at inclusion, were invited from the Outpatient Clinic of Endocrinology or The Eye Photo Clinic at Odense University Hospital (OUH) Svendborg. Diagnosis of diabetes was classified by trained endocrinologists according to international standards with relevant biochemistry. Historical data on urine- and blood samples as well as micro- and macrovascular diabetic complications have been registered consecutively in patients followed at the outpatient clinic in the regional Funen Diabetes Database (FDDB). Data on historical invasive procedures due to cardiac disease were registered in Western Denmark Heart Registry (WDHR). | ||
| T1 | Patients with type 1 diabetes without myocardial infarction, heart failure and symptoms of cardiac disease at inclusion, were invited from the Outpatient Clinic of Endocrinology or The Eye Photo Clinic at OUH Svendborg. Diagnosis of diabetes was classified by trained endocrinologists according to international standards with relevant biochemistry. Historical data on urine- and blood samples as well as micro- and macrovascular diabetic complications have been registered consecutively in patients followed at the outpatient clinic in the regional FDDB. Data on historical invasive procedures due to cardiac disease were registered in WDHR. | ||
| Non-diabetic subjects | Non-diabetic subjects without myocardial infarction, heart failure and symptoms of cardiac disease at inclusion, were included from The Danish Cardiovascular Screening trial (DANCAVAS). A randomized controlled trial with the primary aim to evaluate the health benefits and costeffectiveness of using non-contrast full truncus computer tomography (CT) scans (to measure coronary artery calcification (CAC) and identify aortic/iliac aneurysms) and measurements of the ankle brachial blood pressure index (ABI) as part of a multifocal screening and intervention program for cardiovascular disease in men aged 65-74. |
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| Measure | Description | Time Frame |
|---|---|---|
| Changes in Global Longitudinal Strain (GLS) stratified by Coronary Artery Calcium Score (CAC) in patients with diabetes during one year of follow-up | To evaluate the changes in GLS stratified by CAC during one year of follow-up in patients with diabetes compared to non-diabetic subjects | baseline, 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in GLS stratified by Coronary Flow Velocity Reserve (CFVR) in patients with diabetes during one year of follow-up | To evaluate the changes in GLS stratified by CFVR during one year of follow-up in patients with diabetes compared to non-diabetic subjects | baseline, 12 months |
| Correlation between biomarkers and GLS stratified by CFVR |
| Measure | Description | Time Frame |
|---|---|---|
| Relationship between strain values and framerate | To evaluate the changes in strain values dependant of framerate | baseline, 12 months |
| Relationship between strain values and omitted myocardial segments |
Inclusion criteria:
Exclusion criteria:
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Patients with diabetes type 1+2 and non-diabetic subjects from the DANCAVAS trial (NCT00662480)
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| Name | Affiliation | Role |
|---|---|---|
| Kenneth Egstrup, DMSci | Odense University Hospital (OUH) Svendborg Hospital | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cardiovascular Research Unit, OUH Svendborg Hospital | Svendborg | 5700 | Denmark |
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| ID | Term |
|---|---|
| D018487 | Ventricular Dysfunction, Left |
| D003922 | Diabetes Mellitus, Type 1 |
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D018754 | Ventricular Dysfunction |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D003920 | Diabetes Mellitus |
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Storage in biobank (-80° C):
5 x 2 ml (serum).
4 x 2 ml (ethylenediaminetetraacetic acid).
2 x 2 ml (sodium citrate)
1 x 2 ml (erythrocyte sedimentation rate)
To evaluate the correlation between biomarkers (C-Reactive Protein, Troponin T, NT-proBNP and Uric Acid) and GLS stratified by CFVR in diabetic patients compared to non-diabetic subjects |
| 12 months |
| Correlation between biomarkers and GLS stratified by CAC | To evaluate the correlation between biomarkers (C-Reactive Protein, Troponin T, NT-proBNP and Uric Acid) and GLS stratified by CAC in diabetic patients compared to non-diabetic subjects | 12 months |
| Changes in LV function stratified by CAC | To evaluate LV systolic and diastolic function stratified by CAC in patients with diabetes compared to non-diabetic subjects. | baseline, 12 months |
| Changes in LV function stratified by CFVR | To evaluate LV systolic and diastolic function stratified by CFVR in patients with diabetes compared to non-diabetic subjects. | baseline, 12 months |
| Changes in LV function stratified by micro- and macrovascular diabetic status | To evaluate changes in LV systolic and diastolic function in relation to albuminuria, retinopathy, neuropathy, diabetes duration and CAC. | baseline, 12 months |
| Correlation between CFVR and Free Fractional Reserve -Computed Tomography (FFR-CT) | To evaluate the correlation between CFVR and FFR-CT in a subgroup consisting of diabetic patients and non-diabetic subjects. | baseline |
| Correlation between GLS and FFR-CT | To evaluate the correlation between GLS and non-invasive FFR-CT in a subgroup consisting of diabetic patients and non-diabetic subjects. | baseline |
| Changes in GLS in patients with long-term diabetes and no macrovascular disease | To evaluate the impact of historical varying levels of HbA1c and cholesterols on GLS at baseline in patients with diabetes and no macrovascular disease. | baseline |
To evaluate the changes in strain values dependant of number of myocardial segments omitted
| baseline, 12 months |
| Correlation between dysglycaemia and Left Ventricle Mass (LVM) | To evaluate the impact of dysglycaemia on LVM in non-diabetic subjects compared to diabetic patients. | Baseline |
| Left Ventricle (LV) and Left Atrial (LA) function stratified by New York Heart Association (NYHA) functional class | To evaluate LV and LA systolic and diastolic function in relation to NYHA classification | baseline |
| Changes in cardiac systolic and diastolic function stratified by CAC during five years of follow-up in patients with diabetes | To evaluate the changes in cardiac systolic and diastolic function stratified by CAC during five years of follow-up in patients with diabetes compared to non-diabetic subjects. | baseline, 60months |
| Changes in cardiac systolic and diastolic function stratified by CFVR during five years of follow-up in patients with diabetes | To evaluate the changes in cardiac systolic and diastolic function stratified by CFVR during five years of follow-up in patients with diabetes compared to non-diabetic subjects. | baseline, 60months |
| Changes in cardiac systolic and diastolic function stratified by plaque morphology during five years of follow-up in patients with diabetes | To evaluate the changes in cardiac systolic and diastolic function stratified by plaque morphology during five years of follow-up in patients with diabetes compared to non-diabetic subjects. | baseline, 60months |
| LA function stratified by CFVR | To evaluate atrial function stratified by CFVR in patients with diabetes compared to non-diabetic subjects. | baseline |
| LA function stratified by micro- and macrovascular status | To evaluate atrial function in relation to albuminuria, retinopathy, neuropathy, diabetes duration and CAC. | baseline |
| D044882 |
| Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |