Cardiac Rest and Stress Metabolism in Patients With Type 2 Diabetes
CardioMET
1 other identifier
observational
8
1 country
1
Brief Summary
The number of people with diabetes is rising. One of the major causes of premature death in diabetes is heart failure (HF). This is when the heart cannot pump blood effectively, and this may be related to abnormalities in energy production in the heart muscle. In healthy people, the heart muscle cells show flexibility and can use both sugar and fat molecules for energy production. Although burning fat provides more energy, this process requires more oxygen than burning sugars. As a result, fat is a less efficient fuel for the heart compared to sugars, especially in situations where the energy and oxygen needs are higher, such as during exercise. The investigators propose that the heart muscle in patients with type 2 diabetes relies heavily on fat for energy provision, and fails to burn more sugar molecules for energy provision during exercise to more efficiently use oxygen. Fat and sugar uptake by the heart can be detected by the difference between the blood sugar and fat levels delivered to the heart and returning from the heart, both at rest and also when the heart is working faster during Dobutamine infusion. Dobutamine is a drug frequently used to mimic exercise, and get the heart running faster during medical tests. To test the hypothesis, the investigators will assess fat and sugar uptake by the heart at rest and when the heart is running faster, in patients with type 2 diabetes undergoing investigations to rule out coronary disease. Heart function, and blood supply to heart muscle, at rest and during Dobutamine infusion, will also be measured using MRI scanning. The same tests will be performed in people without diabetes for comparison. It will help understand diabetic heart disease and which aspects may be targeted with new treatments.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Mar 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 5, 2018
CompletedFirst Submitted
Initial submission to the registry
July 2, 2019
CompletedFirst Posted
Study publicly available on registry
July 5, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2020
CompletedMay 3, 2021
April 1, 2021
2 years
July 2, 2019
April 29, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
The difference in myocardial FA extraction fraction (%) between T2D patients and non-diabetic controls at rest.
Myocardial extraction fraction
Immediate at rest and stress
Study Arms (2)
Type 2 Diabetes
Non Diabetic
Interventions
Metabolism in T2DM vs non diabetic
Eligibility Criteria
Group 1. Patients with T2D and no significant CAD (\<50% luminal stenosis on coronary angiography) Group 2. Non-diabetic individuals with no significant CAD (\<50% luminal stenosis on coronary angiography)
You may qualify if:
- Group 1: Type 2 diabetes cohort:
- Participant is willing and able to give informed consent for participation in the study.
- Aged 18 years or above.
- Confirmed diagnosis of T2D according to World Health Organisation (WHO) criteria
- Able (in the investigator's opinion) and willing to comply with all study requirements
- Must understand written and verbal English
- Group 2: Non-diabetic Controls
- Participant is willing and able to give informed consent for participation in the study.
- Aged 18 years or above.
- Able (in the investigator's opinion) and willing to comply with all study requirements.
You may not qualify if:
- Group 1
- Type 1 diabetes.
- Significant CAD\> (50% luminal stenosis)
- Significant renal impairment (eGFR\<30ml/min/m2).
- Previous coronary artery bypass grafting surgery or myocardial infarction
- Significant clinical established diagnosis of heart failure and EF \<40%
- Female participants who are pregnant, lactating or planning pregnancy during the course of the study.
- Participants who have participated in another research study involving an investigational product in the past 12 weeks
- Atrial fibrillation.
- Contra-indications to magnetic resonance imaging (pacemaker, cranial aneurysm clips, metallic ocular foreign bodies, severe claustrophobia).
- Known hypersensitivity to dobutamine or gadolinium.
- Participants with a diagnosis of significant (\>moderate,) valve disease.
- \. Patients who are on Insulin therapy, or oral Thiazolidinedione. 2. Involvement in other studies thought to compromise resulting study data or the health of the participant in the opinion of investigator.
- Group 2
- As per group 1 plus
- +1 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Glenfield Hospital, University Hospitals of Leicester NHS Trust
Leicester, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 2, 2019
First Posted
July 5, 2019
Study Start
March 5, 2018
Primary Completion
March 1, 2020
Study Completion
March 1, 2020
Last Updated
May 3, 2021
Record last verified: 2021-04
Data Sharing
- IPD Sharing
- Will not share