ATOMIC: "Atriogenic Tricuspid Selected, Omics Profile, Multimodality Imaging and Clinical Outcomes"

Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05724225
Collaborator
(none)
60
1
26.7
2.2

Study Details

Study Description

Brief Summary

The aim of our study is to investigate the molecular mechanisms underlying remodeling of the tricuspid valve apparatus in patients with ITF and isolated AF, in comparison with patients with ITF from right ventricular remodeling, patients with atriogenic MI and left ventricular remodeling. To achieve these aims, markers obtained from cardiovascular imaging methods, such as 3D echocardiogram, and biomarkers isolated from the peripheral blood of the study participants will be considered.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Advances in echocardiography and, in particular, the development of three-dimensional echocardiography have allowed a more accurate analysis of the morphology of the tricuspid valve and a detailed understanding of the mechanisms underlying its insufficiency. From a clinical point of view, ITF is divided into a primary form, less frequent (8-10%), caused by primary alterations of the tricuspid valve apparatus, acquired or congenital, and in a "functional" form, the most frequent, conventionally associated in most cases with coexisting pathologies of the left heart or primitive pathologies of the right heart. More recently, long-lasting persistent atrial fibrillation (AF) has been associated with the development of ITF in the presence of structurally normal valve leaflets, preserved right ventricular size and function, and right atrial dilatation. This form of ITF, defined as "atrial functional", could benefit from a different therapeutic management compared to the classic form, more commonly caused by right ventricular dilatation and dysfunction ("ventricular functional" IT). However, not all patients with AF and tricuspid annulus dilatation develop valvular insufficiency and, on the other hand, with the same valvular annulus dilatation and right atrial size, the prevalence of severe IT forms is extremely variable.

    This could depend on different adaptive mechanisms implemented by the valve leaflet tissue that lead to their growth or not in response to atrial remodeling and valve annulus dilatation, representing a key factor in the development and progression of the disease. Atriogenic ITF. If confirmed, these observations could lead to a better prognostic classification and different therapeutic perspectives for patients with AF at risk of developing forms of severe ITF and congestive heart failure.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    60 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Atriogenic Tricuspid Regurgitation, Selected Omics Profile, Multimodality Imaging and Clinical Outcomes (the ATOMIC Study)
    Actual Study Start Date :
    Oct 6, 2021
    Actual Primary Completion Date :
    Nov 7, 2022
    Anticipated Study Completion Date :
    Dec 29, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    First group with atrial fibrillation disease

    10 Atrial fibrillation(AF), predominant right atrial dilatation with at least moderate IT

    Second group with atrial fibrillation disease and tricuspid insufficiency

    10 AF, predominantly right atrial dilatation without TI (or TI no more than mild)

    Third group with AF and mitral insufficiency

    10 AF, predominantly left atrial dilatation with at least moderate MI

    Fourth group with atrial fibrillation and IM

    10 AF, predominantly left atrial dilatation without MI (or no more than mild MI)

    Fifth group with tricuspid insufficiency

    10 IT at least moderate to right ventricular remodeling in patients with pulmonary hypertension

    Sixth group with mitral insufficiency

    10 MI at least average from left ventricular remodeling from left ventricular dysfunction

    Outcome Measures

    Primary Outcome Measures

    1. Protein expression [1 years]

      Evaluation of the protein expression of the altered biomarkers in the 6 study groups

    Secondary Outcome Measures

    1. Correlation between circulating protein biomarkers and diagnostic parameters [6 months]

      Analysis of the correlation between circulating protein biomarkers and echocardiographic parameters of mitral and tricuspid valve leaflet remodeling

    2. Correlation between clinical data and diagnostic imaging markers [6 months]

      Evaluation of the correlation between clinical data (gender, age, AF duration) and echocardiographic imaging markers

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Admitted to the Department of cardiological, neurological and metabolic sciences of the San Luca hospital with a diagnosis of persistent atrial fibrillation
    Exclusion Criteria:
    • Patient aged <18 years;

    • Pregnancy;

    • Chronic inflammatory diseases;

    • Autoimmune diseases;

    • Tumor diseases;

    • Chronic renal failure with eGFR < 30 mL/min;

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Istituto Auxologico Italiano IRCSS Ospedale San Luca Milano Italy 20149

    Sponsors and Collaborators

    • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Pedicino Daniela, Principal Investigator, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
    ClinicalTrials.gov Identifier:
    NCT05724225
    Other Study ID Numbers:
    • 4424
    First Posted:
    Feb 13, 2023
    Last Update Posted:
    Feb 15, 2023
    Last Verified:
    Feb 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Pedicino Daniela, Principal Investigator, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 15, 2023