Allograft Dysfunction in Heart Transplant

Sponsor
Paul Kim (Other)
Overall Status
Recruiting
CT.gov ID
NCT03102125
Collaborator
(none)
376
1
4
54
7

Study Details

Study Description

Brief Summary

The investigators will evaluate for early evidence of cardiac allograft dysfunction by cardiac MRI and single cell sequencing to determine underlying molecular and macroscopic causes.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Adult heart-transplant patients, excluding those with a GFR less than 30 mL/min/1.73m2, contraindications to MRI and allergies to either regadenoson or gadolinium contrast, will be enrolled over 60 months. Patients will be recruited from UCSD. The investigators will specifically enroll all eligible heart-transplant patients.

Brief protocol:

Cardiac MRI is performed. Cine images in standard views are obtained. T1 and T2 mapping sequences are performed on short axis images pre- and post-gadolinium contrast. For stress imaging, intravenous regadenoson is given as a 0.4 mg bolus followed by a 5 mL saline flush. After 30 seconds, short-axis images are acquired for 30 consecutive heartbeats with administration of gadolinium. Rest imaging is performed 30 minutes after stress imaging. Lastly, late gadolinium enhancement images are obtained in standard views. Images are analyzed offline by a blinded independent reader. Patients will be followed for at least 1 year after enrollment for MACE.

Peripheral blood and endomyocardial biopsies will also be collected, timing as per usual clinical care as well as for-cause, for single cell RNAseq analyses.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
376 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Diagnostic
Official Title:
Defining Mechanisms for Cardiac Allograft Dysfunction to Improve Allograft Longevity and Survival in Heart-Transplant Patients
Actual Study Start Date :
Oct 1, 2019
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
Apr 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Nonspecific allograft dysfunction

Patients with nonspecific allograft dysfunction will undergo stress cardiac MRI with regadenoson in addition to performing late gadolinium enhancement and obtaining mean segmental T1 values of the heart. Peripheral blood and endomycardial biopsies will also be obtained for single cell RNAseq analyses.

Drug: Regadenoson
For use in stress myocardial perfusion imaging.
Other Names:
  • Lexiscan
  • Experimental: Normal graft function

    Patients with normal graft function will undergo stress cardiac MRI with regadenoson in addition to performing late gadolinium enhancement and obtaining mean segmental T1 values of the heart. Peripheral blood and endomycardial biopsies will also be obtained for single cell RNAseq analyses.

    Drug: Regadenoson
    For use in stress myocardial perfusion imaging.
    Other Names:
  • Lexiscan
  • Experimental: Cardiac allograft vasculopathy

    Patients with allograft dysfunction from known cardiac allograft dysfunction will undergo stress cardiac MRI with regadenoson in addition to performing late gadolinium enhancement and obtaining mean segmental T1 values of the heart. Peripheral blood and endomycardial biopsies will also be obtained for single cell RNAseq analyses.

    Drug: Regadenoson
    For use in stress myocardial perfusion imaging.
    Other Names:
  • Lexiscan
  • Experimental: ACR/AMR

    Patients with allograft dysfunction from prior episodes of acute cellular or antibody mediated rejection will undergo stress cardiac MRI with regadenoson in addition to performing late gadolinium enhancement and obtaining mean segmental T1 values of the heart. Peripheral blood and endomycardial biopsies will also be obtained for single cell RNAseq analyses.

    Drug: Regadenoson
    For use in stress myocardial perfusion imaging.
    Other Names:
  • Lexiscan
  • Outcome Measures

    Primary Outcome Measures

    1. Myocardial Perfusion Reserve [60 months]

    Secondary Outcome Measures

    1. Rest and stress myocardial blood flow [60 months]

    2. LGE % [60 months]

    3. LVEF [60 months]

    4. LV end-diastolic volume index [60 months]

    5. LV mass index [60 months]

    6. native T1 and T2 myocardial values [60 months]

    7. extracellular volumes [60 months]

    8. myocardial strain rate [60 months]

    Other Outcome Measures

    1. Major adverse cardiovascular events [60 months]

      death, re-transplantation, percutaneous coronary intervention and HF hospitalization

    2. Percentage of different T-cell subsets by single cell RNAseq [60 months]

    3. Number of stenotic microvasculopathy by histopathologic review of endomyocardial biopsy samples [60 months]

      Each endomyocardial biopsy slide will be reviewed for stenotic microvasculopathy as per Hiemann et al 2007, Circulation. 1 stenotic blood vessel per view on X200 zoom is diagnostic of stenotic microvasculopathy.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age greater than or equal to 18 years old.

    • At least three months status post heart transplantation.

    Exclusion Criteria:
    • Biopsy proven acute rejection episode in the past 3 months.

    • Patients with symptoms or signs of acute myocardial ischemia or recent acute coronary syndrome in the past 3 months.

    • Uncontrolled obstructive ventilatory disease including asthma and COPD.

    • History of generalized tonic-clonic seizures.

    • Second or third degree AV nodal block.

    • Sinus node dysfunction.

    • Contraindications to MRI including cardiovascular implantable electronic devices.

    • Renal dysfunction with an estimated GFR less than 30 mL/min/1.73m2.

    • Prior adverse reaction to either regadenoson or gadolinium contrast. Prior adverse reaction to adenosine or dipyridamole will be assessed on a case-by-case basis.

    • Systolic blood pressure greater than 180 or less than 85 mmHg.

    • Diastolic blood pressure greater than 120 or less than 40 mmHg.

    • Resting heart rate greater than 120 or less than 45 beats per minute. - Severe claustrophobia.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UC San Diego La Jolla California United States 92037

    Sponsors and Collaborators

    • Paul Kim

    Investigators

    • Principal Investigator: Paul Kim, MD, UC San Diego

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Paul Kim, Assistant Professor, University of California, San Diego
    ClinicalTrials.gov Identifier:
    NCT03102125
    Other Study ID Numbers:
    • 160808
    First Posted:
    Apr 5, 2017
    Last Update Posted:
    Nov 4, 2021
    Last Verified:
    Nov 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Paul Kim, Assistant Professor, University of California, San Diego
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 4, 2021