Links Between Inflammation and Cardiometabolic Diseases

Sponsor
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
Overall Status
Recruiting
CT.gov ID
NCT01934660
Collaborator
(none)
480
1
187.4
2.6

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase

    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).

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    480 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Inflammatory Characterization of Known or Possible Cardiovascular Diseases
    Actual Study Start Date :
    Dec 2, 2013
    Anticipated Primary Completion Date :
    Jul 15, 2029
    Anticipated Study Completion Date :
    Jul 15, 2029

    Arms and Interventions

    Arm Intervention/Treatment
    Group 1

    Healthy volunteers

    Group 2

    Subjects diagnosed with diabetes

    Group 3

    Subjects diagnosed cardiovascular disease

    Outcome Measures

    Primary Outcome Measures

    1. 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

    1. 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)

    2. 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

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    • Cardiovascular Disease Eligibility Criteria
    INCLUSION CRITERIA:
    • Females and males 18 years of age or older

    • Diagnosis of clinical CAD (including abnormal EKG with a prior infarction pattern, abnormal echo consistent with a wall motion abnormality or a referral note from cardiologist with diagnosis of CAD)

    • CAD that is currently stable (defined by no change in medications for blood pressure, angina or diuretic therapy or in no new CV symptoms over the past month in a patient who has had a primary cardiac event or an abnormal EKG with confirmed wall motion abnormality)

    • CAD which may be associated with chronic stable angina (defined by a clinical syndrome characterized by discomfort in the chest, jaw, shoulder, back, or arm by a physician).

    • CAD that is found on CCTA which may be subclinical

    EXCLUSION CRITERIA:
    • Pregnant women or lactating women.

    • For optional adipose biopsy, any subject with known bleeding disorder, current fever or on anti-coagulation.

    • For optional MRI, inability to participate due to metal within body, claustrophobia, or anything else that prohibits undergoing a MRI scan

    • Any solid organ or liquid tumor within the past five years, with the exception of nonmelanomatous skin cancer,

    • Active infectious diseases within 3 months requiring antibiotics, collagen vascular diseases such as RA, psoriasis and mixed connective tissue diseases and immune-mediated lung diseases (e.g. IPF, BOOP)

    • A BMI >40 kg/m(2) due to PET MRI restrictions

    • Subjects with severe renal excretory dysfunction, estimated glomerular filtration rate < 30 mL/min/1.73m(2) body surface area according to the Modification of Diet in Renal Disease criteria, will not receive the cardiac CT angiography, or gadolinium contrast agent during the PET/MRI.

    Diabetes Mellitus Eligibility Criteria

    INCLUSION CRITERIA:
    • Females and males 18 years of age or older

    • Diagnosis of type 2 diabetes mellitus (DM), currently stable as defined by no change in antidiabetic medications over the past month and fasting glucose <200

    EXCLUSION CRITERIA:
    • Pregnant women and or lactating women.

    • For optional adipose biopsy, any subject with known bleeding disorder, current fever or on anti-coagulation.

    • For optional MRI, inability to participate due to metal within body, claustrophobia, or anything else that prohibits undergoing a MRI scan

    • Any solid organ or liquid tumor within the past five years, with the exception of nonmelanomatous skin cancer,

    • Active infectious diseases within 3 months requiring antibiotics, collagen vascular diseases such as RA, psoriasis and mixed connective tissue diseases and immune-mediated lung diseases (e.g. IPF, BOOP)

    • A BMI >40 kg/m(2) due to PET MRI restrictions

    • Subjects with severe renal excretory dysfunction, estimated glomerular filtration rate < 30 mL/min/1.73m(2) body surface area according to the Modification of Diet in Renal Disease criteria, will not receive the cardiac CT angiography, or gadolinium contrast agent during the PET/MRI.

    • Subjects with second -or third-degree AV block or sinus node dysfunction will not receive the 13N-ammonia PET/CT imaging unless these patients have a functioning artificial pacemaker.

    • Subjects with any signs or symptoms of acute coronary syndrome, including vasoreactive hypertension with blood pressure exceeding 180/100, any concerning ST segment changes on ECG, or acute chest pain, will not receive the 13N-ammonia PET/CT imaging.

    Healthy Volunteers:
    INCLUSION CRITERIA:

    -Females and males 18 years of age or older without any clinical diagnosis of a chronic health condition that is knownto accelerate vascular disease beyond traditional risk factors including lung disease or active infection

    EXCLUSION CRITERIA:
    • For imaging studies, pregnant women

    • For imaging studies, lactating women

    • For optional MRI, inability to participate due to in optional MRI metal within body, claustrophobia, or anything else that prohibits undergoing a MRI scan

    • Any solid organ or liquid tumor within the past five years, with the exception of non melanomatous skin cancer,

    • Active infectious diseases within 3 months requiring antibiotics, collagen vascular diseases such as RA, psoriasis and mixed connective tissue diseases and immune-mediated lung diseases (e.g. IPF, BOOP)

    • Clinical diagnosis of diabetes or cardiovascular disease

    • Fasting glucose >125,

    • LDL>200,

    • LFT s 3 times normal limit,

    • eGFR<60,

    • Subjects with severe renal excretory dysfunction will not receive the cardiac CT angiography, or gadolinium contrast agent during the PET/MRI.

    • A BMI >40 kg/m(2) due to PET MRI restrictions.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Institutes of Health Clinical Center Bethesda Maryland United States 20892

    Sponsors and Collaborators

    • National Heart, Lung, and Blood Institute (NHLBI)

    Investigators

    • Principal Investigator: Michael N Sack, M.D., National Heart, Lung, and Blood Institute (NHLBI)

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    National Heart, Lung, and Blood Institute (NHLBI)
    ClinicalTrials.gov Identifier:
    NCT01934660
    Other Study ID Numbers:
    • 130194
    • 13-H-0194
    First Posted:
    Sep 4, 2013
    Last Update Posted:
    Aug 5, 2022
    Last Verified:
    Aug 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by National Heart, Lung, and Blood Institute (NHLBI)
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 5, 2022