Analysis of Calcium Score of Severe Aortic Stenosis in Patients With and Without Cardiac Amyloidosis (CAUSATIVE Study)

Sponsor
University Hospital of Ferrara (Other)
Overall Status
Recruiting
CT.gov ID
NCT06066632
Collaborator
(none)
480
1
12
39.9

Study Details

Study Description

Brief Summary

The concomitant presence of cardiac amyloidosis (CA) in patients with aortic stenosis (AS) may challenge the estimation of stenosis degree. In patients with dual pathology (AS + CA) the most frequent AS hemodynamic profile is paradoxical low-flow, low-gradient AS.

In this setting, estimating stenosis degree with cardiac ultrasound may be challenging and aortic valve calcium score estimation by cardiac CT is a valuable exam.

Preliminary findings from small case series showed that patients with severe AS and CA presented less valvular calcium deposition compared to patients with severe AS alone. On this basis, confirmation of these findings would have a huge clinical impact on diagnosis, choice of treatment strategy and understanding of the pathophysiology of these patients.

The aim of the study is to study the correlation between valvular calcium score (assessed by EKG-gated CT) and effective orifice area (assessed through echocardiogram) according to cardiac amyloidosis presence (in the overall population and among hemodynamic phenotypes of cardiac amyloidosis).

As secondary endpoints the study will sought to assess TAVI/SAVR efficacy, procedural complications, in-hospital mortality, all-cause death and heart failure hospitalization at 1 year, according to absence or presence of CA.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Aortic stenosis (AS) is the most common valvular pathology in the elderly population, and there is an anticipated increase in prevalence and associated costs for treating this condition in the future. In a non-negligible percentage of cases (approximately 15%), another pathology is associated, namely cardiac amyloidosis, especially in the wild-type ATTR form. Patients with both pathologies (AS+ATTR) have a worse prognosis compared to those with AS alone. Based on the available data up to now, ATTR-associated amyloidotic cardiomyopathy does not appear to significantly influence the immediate outcome of TAVI or short-term outcomes. However, among patients with amyloidosis, there is an increased frequency of heart failure in subsequent follow-ups. The mechanism behind this dual pathology remains unclear. Epidemiological similarities (advanced age) alone do not explain the association. It is possible that there is a direct causal link between amyloidosis and aortic stenosis (amyloidosis as a co-cause or contributing factor to valvular stenosis), or that the elevated intramyocardial strain due to degenerative valvular stenosis promotes amyloidogenesis and myocardial infiltration. Understanding the extent of valvular calcifications in individual cases would provide better insights into the pathogenesis of this dual pathology. There are also diagnostic implications. Amyloidosis could potentially complicate the accurate classification of the severity of aortic pathology. For example, patients with AS+ATTR often exhibit a "low-flow low-gradient" paradoxical hemodynamic profile. In these cases, estimating the valve area with an echocardiogram is challenging, and evaluating the valvular calcium score through CT assumes an important diagnostic role. Preliminary studies suggest that, for the same degree of stenosis severity, there may be a lower quantity of calcium in the valves of patients with AS+ATTR compared to those with AS alone. Preliminary studies suggest that, for the same degree of stenosis severity, there may be a lower quantity of calcium in the valves of patients with AS+ATTR compared to those with AS alone. In a 1:1 propensity matching of over 300 patients (mostly without aortic stenosis), those with amyloidosis had lower aortic valvular calcium scores (p<0.01). In a small series of 13 cases with AS+ATTR, 12 had aortic valvular calcium scores below the severity cut-offs recommended by the guidelines. If confirmed, traditionally used calcium score cut-offs may be inadequate, with significant implications for treatment selection and therefore prognosis.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    480 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Other
    Official Title:
    Analysis of Calcium Score Values of Severe Aortic Stenosis in Patients With and Without Cardiac Amyloidosis (CAUSATIVE Study)
    Actual Study Start Date :
    Jun 1, 2023
    Anticipated Primary Completion Date :
    May 1, 2024
    Anticipated Study Completion Date :
    Jun 1, 2024

    Arms and Interventions

    Arm Intervention/Treatment
    Group 1 - "Dual Pathology"

    Age >65 years Severe aortic stenosis at echocardiographic examination TAVI o SAVR planned or already undergone TAVI/SAVR ECG-gated cardiac CT and echocardiographic examinations available before TAVI/SAVR Cardiac uptake at bone tracer scintigraphy with a Perugini score of 2 or 3.

    Group 2- "Control Group"

    Age >65 years Severe aortic stenosis at echocardiographic examination TAVI o SAVR planned or already undergone TAVI/SAVR ECG-gated cardiac CT and echocardiographic examinations available before TAVI/SAVR Patients with no cardiac uptake at scintigraphy with bone tracer.

    Outcome Measures

    Primary Outcome Measures

    1. Correlation between valvular calcium score and effective orifice area. [Up to 12 months]

      Correlation between valvular calcium score (assessed by EKG-gated CT) and effective orifice area (assessed through echocardiogram) according to cardiac amyloidosis presence (in the overall population and among hemodynamic phenotypes of cardiac amyloidosis).

    Secondary Outcome Measures

    1. TAVI/SAVR efficacy [At time of post-procedural echocardiographic assessment (through study completion, an average of 1 month)]

      Echocardiographic mean and maximal aortic gradient (mmHg) will be assessed.

    2. TAVI/SAVR efficacy [At time of post-procedural echocardiographic assessment (through study completion, an average of 1 month)]

      Echocardiographic effective orifice valvular area (EROA) will be assessed and reported in cm2.

    3. Procedural Complications [At an average of 12 months]

      Procedural complications will be assessed as per VARC definitions

    4. In-hospital Mortality [At an average of 12 months]

      In-hospital Mortality will be assessed from hospital records

    5. All-cause Mortality and Heart Failure Hospitalization [At an average of 12 months]

      The composite of all-cause Mortality and Heart Failure Hospitalization will be assessed through clinical follow-up, hospital records, and telephone follow-up.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • signed informed consent

    • age ≥65 years old

    • severe AS

    • planned or performed TAVI/SAVR

    • at least one red-flag suggestive of CA

    • availability of EKG-gated CT

    • availability of echocardiogram performed before TAVI/SAVR

    • availability of bone scintigraphy performed within 1 year from CT

    Exclusion Criteria:

    • suboptimal acoustic window that may undermine the assessment of AS severity and phenotype profiling

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital of Ferrara Ferrara Italy 44124

    Sponsors and Collaborators

    • University Hospital of Ferrara

    Investigators

    • Principal Investigator: Matteo Serenelli, Doctor, Azienda Ospedaliero Universitaria di Ferrara

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Matteo Serenelli, Doctor, University Hospital of Ferrara
    ClinicalTrials.gov Identifier:
    NCT06066632
    Other Study ID Numbers:
    • 72/2022/Oss/AOUFe
    First Posted:
    Oct 4, 2023
    Last Update Posted:
    Oct 4, 2023
    Last Verified:
    Sep 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 Matteo Serenelli, Doctor, University Hospital of Ferrara
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 4, 2023