Links Between Inflammation and Cardiometabolic Diseases
- Conditions
- Healthy VolunteerInflammationDiabetes MellitusCardiovascular Disease
- Interventions
- Drug: 13N-amonia
- Registration Number
- NCT01934660
- Brief Summary
Background:
- Cardiometabolic diseases are a combination of medical disorders that, when they occur together, increase the risk of heart disease and diabetes. Researchers want to learn if there is a relationship between these diseases and inflammation (redness, swelling, and pain). Inflammation affects the entire body. Researchers will study this relationship in people with heart disease and diabetes, and compare it to healthy people.
Objectives:
- To learn if there are links between inflammation and cardiometabolic diseases.
Eligibility:
* Adults 18 years of age or older with heart disease or diabetes.
* Healthy volunteers 18 years of age or older.
Design:
* Participants will have up to six study visits. There will be first visit, then an optional visit 12 months after the first visit.
* At the study visits they will have:
* Blood taken with a needle in their arm.
* An electrocardiogram. Small patches are stuck to the chest and limbs. A machine measures electrical signals of the heart.
* Completed a number of questionnaires.
* A body scan called an FDG PET/CT. A substance will be injected through a tube in their arm. They will lie on a special bed that will move in and out of the PET/CT scanner. The PET/CT scanner will take pictures of the body. The scan will last up to 30 minutes.
* Some participants will have other body scans ( FDG PET/MRI). The procedures are similar to the FDG PET/CT scan. These other scans will last about 30 minutes total.
* Some participants will also have a CT scan of their heart. A substance will be injected through a tube in their arm. They will lie on a table in a large, donut-shaped machine. An X-ray tube will move around their body, taking many pictures. This procedure can last up to 2 hours.
* Some participants will have tests that measures blood pressure and how the blood moves through the body.
* Some participants will have small samples of skin and fat tissue taken.
- Detailed Description
Over the past two decades, the number of subjects with cardiometabolic diseases (CMD) such as atherosclerotic cardiovascular disease (CVD), dyslipidemia, insulin resistance and diabetes have been rising. Characterizing these disease states reveals that inflammation is a common feature of CMD; however, mechanistic links between inflammation and these disease states in humans remain poorly understood. In this protocol, we aim to characterize inflammation within the blood vessels, blood, fat and skin in diabetes and coronary artery disease compared to those without disease. We hypothesize that diabetes and coronary disease will be systemic inflammatory states and will provide an important frame of reference for parameters found on novel imaging techniques in another ongoing protocol trying to understand how skin inflammation affects risk for CMD and CVD (13-H-0065).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 150
Not provided
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Group 1 Fludeoxyglucose F18 Healthy volunteers Group 1 13N-amonia Healthy volunteers Group 2 Fludeoxyglucose F18 Subjects diagnosed with diabetes Group 2 13N-amonia Subjects diagnosed with diabetes Group 3 Fludeoxyglucose F18 Subjects diagnosed cardiovascular disease Group 3 13N-amonia Subjects diagnosed cardiovascular disease
- Primary Outcome Measures
Name Time Method Our primary outcome of interest is vascular inflammation measured by standard uptake values from PET/CT and PET/MRI imaging with FDG 1 day to 10 years vascular inflammation measured by standard uptake values from PET/CT and PET/MRI imaging with FDG
- Secondary Outcome Measures
Name Time Method Our secondary outcomes are mean aortic wall thickness at the most diseased segment on FDG PET/CT and vessel wall area on MRI at the most diseased segment, and we will perform analyses using a model including the same variables as above. 1 day to 10 years Mean Aortic Wall Thickness at the most diseased segment (measured by MRI at FDG PET MRI) --Vessel Wall Area at the most diseased segment (measured by MRI at FDG PET MRI)
As a tertiary analysis, we will add novel biomarkers to the above models including HDL efflux, HOMA-IR and inflammatory mediators to understand the association of each biomarker on vascular disease markers 1 day to 10 years to understand the association of each biomarker on vascular disease markers
Trial Locations
- Locations (1)
National Institutes of Health Clinical Center
🇺🇸Bethesda, Maryland, United States