Cardiac Transplant Metabolomics

Sponsor
Western University, Canada (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05772442
Collaborator
Canadian Cardiovascular Society (Other), Bayer (Industry), University of Alberta (Other), Queen's University (Other)
100
13

Study Details

Study Description

Brief Summary

Patient who received a heart transplant may develop organ rejection. Currently, an invasive biopsy of the heart needs to be performed to diagnose rejection. The purpose of this research study is to identify novel metabolic biomarkers that can be developed into a blood test that can identify signs of rejection without doing a heart biopsy.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Extra blood samples (5-10 mL) drawn

Detailed Description

Background:

Cardiac transplantation remains the treatment of choice for end-stage heart failure. Rejection is a major risk factor affecting the outcome and survival in transplant recipients. Endomyocardial biopsy is the gold standard for diagnosis of post-transplantation rejection, but it is an invasive procedure with potential serious complications. Moreover, due to limited catheterization lab time and time required to process biopsied tissue, the transplanted organs could potentially receive irreversible damages upon diagnosis of acute rejection. Current available non-invasive test involving detecting donor DNA in recipient's blood is still costly and has many limitations. Hence, a better non-invasive and timely diagnostic approach with high sensitivity and specificity is needed to help improve the diagnosis of acute post-cardiac transplant rejection.

Methods At the London Health Science Centre, patient who had a cardiac transplant will undergo routine weekly blood sample collection and endomyocardial biopsy for the first 4 weeks to screen for acute rejection. After informed consent was obtained for routine endomyocardial biopsy and research study, endomyocardial tissue samples and blood will be collected from the patient. Two to three biopsy samples and the blood were processed according to the protocols provided by the Metabolomic Innovation Centre (Edmonton, Alberta, Canada). The sample will be analyzed using the high-performance chemical isotope labelling liquid chromatography mass spectrometry metabolomics platform.

Expected Results:

Using the non-targeted metabolomics, the primary objective is to identify promising novel candidate biomarkers from the blood samples that can help us identify patients who are in acute rejection post-cardiac transplant. The blood sample biomarkers can be validated with endomyocardial biopsy metabolomics data. In addition, characterizing the metabolic profile of transplanted heart can provide insights for the myocardial energetics in transplanted heart. These data can potentially help physicians predict the likelihood of patients developing rejection.

Conclusion:

Metabolomics is an emerging technology used for absolute quantification of metabolites in tissues, cells, and biological fluids based on mass spectrometry. Investigators are hoping to use this technology to identify novel candidate biomarkers that can be used to accurately predict the presence of acute rejection in post-cardiac transplant patients.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Investigating the Metabolomic Profile of Transplanted Heart With and Without Pathological Signs of Rejection
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Apr 1, 2024

Arms and Interventions

Arm Intervention/Treatment
No pathological signs of rejection

Diagnostic Test: Extra blood samples (5-10 mL) drawn
Extra blood samples will be sent for metabolomics analysis.

With pathological signs of rejection

Diagnostic Test: Extra blood samples (5-10 mL) drawn
Extra blood samples will be sent for metabolomics analysis.

Outcome Measures

Primary Outcome Measures

  1. Metabolomics differences detected in the blood sample of patient with signs of transplant rejection vs. no rejection. [1-2 year to obtain these samples.]

    25 blood samples in the no rejection group and 25 blood samples in the rejection group will be collected.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All patients with heart transplant undergoing routine endomyocardial biopsy and blood work for transplant rejection screening and workup.

  • Patients or substitute decision makers are able to provide informed consent to agree to participate in this study.

Exclusion Criteria:
  • Patients or substitute decision makers declined to participate in this study.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Western University, Canada
  • Canadian Cardiovascular Society
  • Bayer
  • University of Alberta
  • Queen's University

Investigators

  • Principal Investigator: Stuart Smith, MD, Western University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Western University, Canada
ClinicalTrials.gov Identifier:
NCT05772442
Other Study ID Numbers:
  • 122451
First Posted:
Mar 16, 2023
Last Update Posted:
Mar 22, 2023
Last Verified:
Mar 1, 2023
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 Western University, Canada

Study Results

No Results Posted as of Mar 22, 2023