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In-depth Characterization of Atriogenic Secondary Tricuspid Regurgitation Due to Atrial Fibrillation

In-depth Characterization of Atriogenic Secondary Tricuspid Regurgitation Due to Atrial Fibrillation. Prevalence, Mechanisms, Advanced Quantification of Regurgitation Severity, and Relative Impact of Sinus Rhythm Restoration on the 3D Remodeling of Right Heart Chambers and Tricuspid Valve Apparatus

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05749107
Acronym
ASTRA
Enrollment
1050
Registered
2023-03-01
Start date
2022-12-02
Completion date
2025-11-02
Last updated
2024-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation, Persistent, Heart Valve Incompetence

Keywords

Functional tricuspid regurgitation, Three-dimensional echocardiography, Doppler echocardiography, Right ventricular function, Atrial fibrillation

Brief summary

1050 patients with persistent/permanent atrial fibrillation (AF) will be studied using conventional and advanced (three-dimensional and deformation imaging) echocardiography. Patients with moderate/severe isolated secondary tricuspid regurgitation (STR) will undergo blood tests to assess their proteomic profile and cardiac CT to measure the tricuspid annulus geometry. The project will aim to 1. assess the prevalence of moderate/severe isolated STR in patients with AF; 2. identify the mechanisms associated with the development of moderate-severe STR in patients with AF; 3. identify the proteomic profile associated with significant growth of tricuspid valve leaflets as a mechanism to protect patients with AF from the development of moderate/severe STR; 4. evaluate the effects of the restoration of sinus rhythm on the severity of STR and the remodeling of the right heart cardiac structures (i.e. right ventricle, right atrium, and tricuspid valve apparatus).

Interventions

DIAGNOSTIC_TESTEchocardiography

Identify AF patients at risk of developing moderate/severe STR and those who will benefit from restoring the normal sinus rhythm

COMBINATION_PRODUCTProteomic analyses

To identify the mechanisms leading to moderate/severe STR during AF.

Sponsors

Ministry of Health, Italy
CollaboratorOTHER_GOV
Istituto Auxologico Italiano
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* age\> 18 years * persistent/permanent atrial fibrillation * good acoustic apical window * left ventricular ejection fraction \> 50% * pulmonary artery systolic pressure\< 50 mm Hg * no more than mild mitral or aortic valve disease * ability to attend clinical and echocardiographic follow-ups * signature of the study informed consent

Exclusion criteria

* pregnancy * implanted pace-maker or ICD * previous heart valve surgery or transcatheter treatment * previous heart transplant * organic tricuspid regurgitation

Design outcomes

Primary

MeasureTime frameDescription
Incidence of either moderate or severe functional tricuspid regurgitation1 yearTo assess the prevalence of moderate or severe atriogenic secondary tricuspid regurgitation (STR) in patients with persistent/permanent atrial fibrillation (AF), and to develop valve-specific metrics and parameters to assess STR severity by echocardiography.
To identify the mechanisms leading to moderate/severe STR during AF.3 yearsSTR severity varies among patients with persistent/permanent AF and comparable RV and RA remodeling. The role of RV and RA size, shape, and function on the extent of tricuspid annulus dilation and dysfunction remains to be clarified. Moreover, it is unknown whether the leaflets of the tricuspid valve can adapt to the stretch exerted on them by the progressive dilation of the tricuspid annulus. The contribution of leaflet adaptation to the pathophysiology of STR and its molecular determinants remains to be clarified
To evaluate the extent of the right heart structure remodeling occurring after the recovery of the sinus rhythm and its effects on STR severity.3 yearsPatients undergoing sustained cardioversion to sinus rhythm (both electrical and pharmacological) and/or ablation of AF, will be followed at 1, 3, and 12 months after the procedure by recording electrocardiogram and complete 2D Doppler and 3DE to assess the extent of the remodeling of the RV, the RA, and the tricuspid valve apparatus. Patients with atriogenic moderate/severe STR without clinical indication to either cardioversion or ablation of the AF, and patients with none/mild atriogenic STR will be followed with clinical assessment, and complete 2D, Doppler and 3DE at 6 months and 1 year. The severity of STR will be quantified by measuring EROA, regurgitant volume, and regurgitant fraction.

Secondary

MeasureTime frameDescription
Development of an interpretable predictive model by using and integrating a variety of statistical and artificial intelligence (AI) techniques.3 yearsClinical, echocardiographic, and biomarker parameters that might predict either the development of moderate/severe STR in patients with AF or the likelihood of reduction of STR severity after cardioversion in sinus rhythm will be identified and integrated in an expert system based on fuzzy reasoning.

Countries

Italy

Contacts

Primary ContactLuigi Badano, MD, Ph.D.
l.badano@auxologico.it+390261911
Backup ContactDenisa Muraru, MD, Ph.D.
luigi.badano@unimib.it+390261911

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026