Coronary Artery Disease, Oxidative Stress, Type 2 Diabetes
Conditions
Keywords
drug effects, Type II Diabetes, Angioplasty, Transluminal, Percutaneous Coronary, Drug Therapy, Heart, physiology, function
Brief summary
The purpose of this study is to determine the effects of pioglitazone, once daily (QD), on heart functioning before, during and after stent implantation.
Detailed description
Type 2 diabetes increases the risk of coronary heart disease at least by two to three fold compared with non-diabetic subjects. Moreover, prospective studies have shown a significant correlation between several glycemic confounders and morbidity from coronary heart disease even in patients without diabetes mellitus. In patients with previously diagnosed coronary heart disease, impaired glucose tolerance was found in 30 to 67 %. The cardiovascular risk of patients with insulin resistance, with or without glucose intolerance has become more and more apparent within recent years and quantitative coronary angiographic studies have revealed a correlation between the severity of coronary heart disease and impaired glucose tolerance. A new pharmaceutical class for the intervention of insulin resistance, the peroxisome proliferator activated receptor (gamma) agonists have been successfully introduced in the treatment of type 2 diabetes. Beyond their metabolic effects on glucose and lipid metabolism, peroxisome proliferator activated receptor (gamma) agonists show to exert a couple of pleiotropic, anti-inflammatory and vasoprotective effects in patients with type 2 diabetes and impaired glucose tolerance. The incidence and severity of peri-procedural myocardial injury during percutaneous coronary interventions with stent implantation in diabetic and in non-diabetic patients is an important prognostic confounder for the patient. Different laboratory biomarkers have been investigated as diagnostic tools for the estimation of the risk of peri-procedural myocardial injury. Recent studies have convincingly demonstrated that the risk of subsequent ischemic heart events is related to the extent of cardiac troponin or CK-MB increase after coronary intervention, and the prognosis for these individuals is usually worse than that for patients who do not develop an increase in these biomarkers. In a recent trial it was shown that pretreatment with atorvastatin could reduce procedural myocardial injury in elective coronary intervention. The incidence of Troponin I increase was 48% in the placebo group compared to 20% in the atorvastatin group. The aim of this study is to investigate the effect of pioglitazone on the incidence of peri-procedural myocardial injury in patients undergoing percutaneous coronary interventions with stent implantation. Total participation time is anticipated to be 3 weeks.
Interventions
DRUGPioglitazone
Pioglitazone 30 mg, tablets, orally, once daily for one week; increased to Pioglitazone 45 mg, tablets, orally, once daily for up to two weeks.
DRUGPlacebo
Pioglitazone placebo-matching tablets, orally, once daily for up to three weeks.
Sponsors
Takeda
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Stable coronary artery disease with planned percutaneous coronary intervention with stent implantation. * Type II-diabetics and/or an IRIS II score greater than or equal to 50 (measure for the identification of patients with insulin resistance and increased vascular risk). * Females of childbearing potential who are sexually active must agree to use adequate contraception, and can neither be pregnant nor lactating from Screening throughout the duration of the study.
Exclusion criteria
* A planned percutaneous coronary intervention with stent implantation less than 15 days after the screening visit. * Planned multi-vessel intervention. * Use of systemic corticosteroids within the last 3 months prior to screening visit. * Anamnestic history of hypersensitivity to the study drugs or to drugs with similar chemical structures. * History of severe or multiple allergies. * Treatment with any other investigational drug within 3 months before trial entry or earlier participation in the present study. * Have had more than one unexplained episode of severe hypoglycemia (defined as requiring assistance of another person due to disabling hypoglycemia) within 6 months prior to screening visit. * Progressive fatal disease. * History of drug or alcohol abuse within the last 10 years. * A history of significant cardiovascular (New York Health Association stage II - IV), respiratory, gastrointestinal, hepatic (alanine aminotransferase greater than 2.5 times the normal reference range), renal (creatinine greater than 1.2 mg/dL in women and greater than 1.5 in men and/or glomerular filtration rate less than 45), neurological, psychiatric and/or hematological disease as judged by the Investigator. * Pre-treatment with peroxisome proliferator-activated receptor (gamma) agonists within the 3 months prior to screening. * If insulin therapy applicable: initiation of insulin therapy within the last 3 months. * If statin therapy applicable: change of medication within the last 4 weeks. * Myocardial infarction within 3 months prior to screening visit. * Blood donation within last 30 days.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of Cardiac Troponin I elevation (greater than 1 upper limit of normal) post-percutaneous coronary intervention with stent implantation. | 24 hours post stent implantation. |
Secondary
| Measure | Time frame |
|---|---|
| Mean peak values of Troponin I and Creatine Kinase (Myocard-type) post-percutaneous coronary intervention with stent implantation. | Hours: 2, 6 and 12 and 24 post stent implantation. |
| Frequency of Doppler-detected microembolism measured by high intensity transient signals during percutaneous coronary intervention with stent implantation (sub-study Jena only). | Duration of stent implantation surgery. |
| Time course of Troponin I Laboratory Procedure. | Visits: 2, 3, 4, 5, 6, 7, and 8 or Final Visit. |
| Time course of high-sensitive-C-Reactive Peptide Laboratory Procedure. | Visits: 2, 3, 4, 5, 6, 7, and 8 or Final Visit. |
| Time course of nitrotyrosine Laboratory Procedure. | Visits: 2, 3, 4, 5, 6, 7, and 8 or Final Visit. |
| Incidence of Creatine Kinase (Myocard-type) post-percutaneous coronary intervention with stent implantation. | 24 hours post stent implantation. |
| Time course of E-selectin Laboratory Procedure. | Visits: 2, 3, 4, 5, 6, 7, and 8 or Final Visit. |
| Time course of Myoglobin Laboratory Procedure. | Visits: 2, 3, 4, 5, 6, 7, and 8 or Final Visit. |
| Time course of Visfatin Laboratory Procedure. | Visits: 2, 3, 4, 5, 6, 7, and 8 or Final Visit. |
| Time course of Proinsulin intact Laboratory Procedure. | Visits: 1 and 7 or Final Visit. |
| Time course of Adiponectin Laboratory Procedure. | Visits: 1 and 7 or Final Visit. |
| Time course of Asymmetric dimethylarginine Laboratory Procedure. | Visits: 2, 3, 4, 5, 6, 7, and 8 or Final Visit. |
Countries
Germany
Outcome results
None listed