Trajectories of Cardiac Allograft Vasculopathy After Heart Transplantation
NCT ID: NCT04117152
Last Updated: 2020-09-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1300 participants
OBSERVATIONAL
2004-01-01
2020-06-30
Brief Summary
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Detailed Description
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Cardiac Allograft Vasculopathy (CAV) is the third cause of late mortality and the leading cause of late allograft dysfunction. The field of heart transplantation currently lacks longitudinal description of CAV profiles. Identifying relevant CAV trajectories, or evolution profiles, and their respective determinants is an unmet clinical need. CAV trajectories requires an additional level of understanding and characterization over the current paradigm. Understanding the mechanisms and clinical factors involved in the development of CAV will be useful to provide a more nuanced picture of disease progression, which may ultimately contribute to risk stratification and ultimately guiding the care of HTx patients.
Main Outcome(s) and Measure(s):
* Identification of CAV trajectories after transplantation using an unsupervised latent class mixed modeling. CAV angiograms were recorded per center protocol for all patients after transplantation. CAV was graded according to the current ISHLT classification as CAV 0 (not significant), 1 (mild), 2 (moderate) and 3 (severe).
* Determination of clinical, functional, structural, immunological factors associated with the trajectories. In the derivation cohort, the associations between CAV trajectories and clinical, histological, functional, and immunological parameters at the time of transplantation, during the first year and at one-year post-transplant were assessed using multinomial logistic regression.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Latent class mixed modeling
To identify CAV trajectories after heart transplantation using a contemporary unsupervised trajectory-based approach known as latent class mixed modeling
Eligibility Criteria
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Inclusion Criteria
* Heart recipient over 18 years of age.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Groupe Hospitalier Pitie-Salpetriere
OTHER
European Georges Pompidou Hospital
OTHER
Universitaire Ziekenhuizen KU Leuven
OTHER
Cedars-Sinai Medical Center
OTHER
Paris Translational Research Center for Organ Transplantation
OTHER
Responsible Party
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Principal Investigators
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Alexandre Loupy, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Paris Transplant Group
Locations
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Jon Kobashigawa
Los Angeles, California, United States
Maarten Naesens
Leuven, , Belgium
Paris Transplant Group
Paris, , France
Countries
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References
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Loupy A, Coutance G, Bonnet G, Van Keer J, Raynaud M, Aubert O, Bories MC, Racape M, Yoo D, Duong Van Huyen JP, Bruneval P, Taupin JL, Lefaucheur C, Varnous S, Leprince P, Guillemain R, Empana JP, Levine R, Naesens M, Patel JK, Jouven X, Kobashigawa J. Identification and Characterization of Trajectories of Cardiac Allograft Vasculopathy After Heart Transplantation: A Population-Based Study. Circulation. 2020 Jun 16;141(24):1954-1967. doi: 10.1161/CIRCULATIONAHA.119.044924. Epub 2020 May 4.
Other Identifiers
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ParisTRCOT_CAV
Identifier Type: -
Identifier Source: org_study_id
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