The Role of Mitochondrial Respiration in the Cardioprotective Capacity of IPC in Diabetic and Non-diabetic Patients

Sponsor
University of Aarhus (Other)
Overall Status
Completed
CT.gov ID
NCT02993484
Collaborator
(none)
39
8
26

Study Details

Study Description

Brief Summary

The overall aim of this study is to examine the role of mitochondrial respiration in human diabetic tissue before and after ischemia. Furthermore we will examine the ability of ischemic preconditioning (IPC) to preserve the mitochondrial function and hemodynamic performance of both non-diabetic and diabetic fibers after ischemia. To increase our understanding on the metabolic changes during ischemia in both non-diabetic and diabetic tissue we will use Dimethyl Malonate and examine the impact of this blockade on post-ischemic mitochondrial respiration.

Condition or Disease Intervention/Treatment Phase
  • Drug: Dimethyl Malonate
  • Biological: Ischemic preconditioning
  • Other: Ischemia reperfusion
  • Other: Sham
N/A

Detailed Description

20 diabetic and 20 non-diabetic patients undergoing elective CABG surgery or other heart surgery where extracorporal circulation is used will be included in the study. The patiens will not be given any treatment prior to the operation. During the cardiac surgery a small sample of the heart is routinely removed when the patient is connection to the heart-lung machine. From this tissue sample it is possible to isolate muscle trabeculae which will be used in an atrial strip model and randomized to one of four types of treatment. Simultaneously with the isolation of the trabeculae, a fifth trabecular will be used to assess mitochondrial respiration at baseline. Group 1 will serve as a sham control, group 2 will serve as ischemic control and receive an extended period of hypoxia, Group 3 will be treated with ischemic preconditioning, where short periods of non lethal lack of oxygen will be given directly to the tissue (after removal from the patient) prior to the extended period of hypoxia, Group 4 will receive dimethyl malonate prior to the prolonged hypoxia.

Study Design

Study Type:
Interventional
Actual Enrollment :
39 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Basic Science
Official Title:
The Role of Mitochondrial Respiration in the Cardioprotective Capacity of IPC in Diabetic and Non-diabetic Patients
Study Start Date :
Dec 1, 2016
Actual Primary Completion Date :
Feb 1, 2019
Actual Study Completion Date :
Feb 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: non-diabetic Sham control

Heart tissue obtained from non-diabetic patients undergoing surgery will not receive drugs or ischemia

Other: Sham
Heart tissue will be obtained from patients undergoing heart surgery. The tissue will be used to test the properties of ischemia and different cardioprotective interventions.

Experimental: non-diabetic Ischemia reperfusion

Heart tissue from non-diabetic patients undergoing surgery will not receive drugs but will receive ischemia

Other: Ischemia reperfusion
Heart tissue will be obtained from patients undergoing heart surgery. The tissue will be used to test the properties of ischemia and different cardioprotective interventions.

Experimental: non-diabetic Ischemic preconditioning

Heart tissue from non-diabetic patients undergoing surgery will not receive drugs but will receive short periods of ischemia prior to index ischemia

Biological: Ischemic preconditioning
Heart tissue will be obtained from patients undergoing heart surgery. The tissue will be used to test the properties of ischemia and different cardioprotective interventions.

Experimental: non-diabetic Dimethyl malonate

Heart tissue from non-diabetic patients undergoing surgery will receive a drug (Dimethyl Malonate) prior to index ischemia

Drug: Dimethyl Malonate
Heart tissue will be obtained from patients undergoing heart surgery. The tissue will be used to test the properties of ischemia and different cardioprotective interventions.
Other Names:
  • Dimethyl Malonate; PubChem Substance ID 24848281
  • Experimental: Diabetic Sham control

    Heart tissue obtained from diabetic patients undergoing surgery will not receive drugs or ischemia

    Other: Sham
    Heart tissue will be obtained from patients undergoing heart surgery. The tissue will be used to test the properties of ischemia and different cardioprotective interventions.

    Experimental: Diabetic Ischemia reperfusion

    Heart tissue from diabetic patients undergoing surgery will not receive drugs but will receive ischemia

    Other: Ischemia reperfusion
    Heart tissue will be obtained from patients undergoing heart surgery. The tissue will be used to test the properties of ischemia and different cardioprotective interventions.

    Experimental: Diabetic Ischemic preconditioning

    Heart tissue from diabetic patients undergoing surgery will not receive drugs but will receive short periods of ischemia prior to index ischemia

    Biological: Ischemic preconditioning
    Heart tissue will be obtained from patients undergoing heart surgery. The tissue will be used to test the properties of ischemia and different cardioprotective interventions.

    Experimental: Diabetic Dimethyl malonate

    Heart tissue from diabetic patients undergoing surgery will receive a drug (Dimethyl Malonate) prior to index ischemia

    Drug: Dimethyl Malonate
    Heart tissue will be obtained from patients undergoing heart surgery. The tissue will be used to test the properties of ischemia and different cardioprotective interventions.
    Other Names:
  • Dimethyl Malonate; PubChem Substance ID 24848281
  • Outcome Measures

    Primary Outcome Measures

    1. Mitochondrial respiration of individual complexes [Outcome will be assessed within a year when the inclusion of patients is complete]

      Mitochondrial respiration of individual complexes will serve as primary outcome and will be examined by oxygraph technique.

    Secondary Outcome Measures

    1. Hemodynamic performance [Outcome will be assessed within a year when the inclusion of patients is complete]

      Hemodynamic performance will be measured as contractile force of heart fibers before during and after ischemia.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients undergoing CABG or other surgery where extracorporal circulation will be used.
    Exclusion Criteria:
    • raise in ischemic markers within 4 weeks

    • ejection fraction <30

    • Atrial fibrilation

    • Oral opioid treatment

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Aarhus

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Aarhus
    ClinicalTrials.gov Identifier:
    NCT02993484
    Other Study ID Numbers:
    • Human A-strips Mitochondria
    First Posted:
    Dec 15, 2016
    Last Update Posted:
    Jun 7, 2019
    Last Verified:
    Oct 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 7, 2019