Morpho-functional Cardiac Modifications in Treated Mutated Transthyretin Cardiac Amyloidosis

Sponsor
University of Messina (Other)
Overall Status
Unknown status
CT.gov ID
NCT04387344
Collaborator
Campisi Mariapaola (Other)
25
2
7.4
12.5
1.7

Study Details

Study Description

Brief Summary

Cardiac Amyloidosis (CA) is characterized by a long subclinical phase characterized by deposition of amyloid fibrils in atria, valves and walls of ventricles. Longitudinal dysfunction of the left ventricle (LV) with preserved ejection fraction (EF) is the early phase of CA.

Longitudinal dysfunction mainly involves the LV basal and middle segments with less involvement of the distal segments (apical sparing).

Strain echocardiography (STE) measures myocardial deformation. The technique has been shown to be sensitive for early detection of impaired systolic function and for the study of CA. Additionally, cardiac efficiency (myocardial work) can be derived from myocardial strain data analysis.

In the year 2018, "RNA interferences" (patisiran and inotersen) were included in the list of compassionate therapeutic use programs for exclusive use for the treatment of adult patients with hereditary amyloidosis neuropathy. The aim of our study is to evaluate the morpho-functional modifications with RNA interferences.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Transthoracic echocardiographic images are recorded in the available ultrasound units (Vivid 7 and Vivid 9, GE Ultrasound, Horten, Norways and MyLab - Esaote, Genoa, Italy). The diameters and the wall thicknesses are measured according to the insurance of the American Society of Echocardiography. The images obtained with apical view and in format 4 bedrooms with frame rates (70-80 frames / s) - stored for three cardiac cycles in cine-loop format - will be used for evaluate off-line to evaluate left ventricle deformation in the longitudinal and radial direction, basalelateral, and top segments (post processing) through software already in use and available (Suitestenza, Esaote, Florence, Italy and GE Ultrasound, Horten, Norway).

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    25 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Retrospective
    Official Title:
    Cardiac Modifications in Transthyretin Cardiac Amyloidosis
    Anticipated Study Start Date :
    May 20, 2020
    Anticipated Primary Completion Date :
    Jun 30, 2020
    Anticipated Study Completion Date :
    Dec 30, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Change of Atrial and Ventricular Walls Dimensions [Change from Baseline Wall Thickness to 18 months]

      Measurements (mm) of Interatrial Septum, Ventricular Walls, Coumadin Ridge, Mitro-aortic Lamina, Valves

    2. Change of Atrial and Ventricular Strain [Change from Baseline Atrial and Ventricular Strain to 18 months]

      Mean paired change in myocardial strain (percent) by echocardiographic strain-rate imaging (unitless)

    Secondary Outcome Measures

    1. Change of Myocardial Work index of Left Ventricle [Change from Baseline Myocardial work to 18 months]

      Evaluation of the Global work index (GWI): total work within the area of the LV pressure-strain loops calculated from mitral valve closure to mitral valve opening.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • presence of data obtained from historical records of patients who retrospectively met the prescriptive (neurological) criteria and received the prescription of the drugs in question (RNA interferences) having

    • Cardiological evaluation (examination ECG, echocardiography) at the time of prescription

    • Cardiological evaluation (examination ECG, echocardiography) evaluated six months after therapy,

    • Cardiological evaluation (examination ECG, echocardiography) evaluated 12-18 months after therapy,

    Exclusion Criteria:
    • it wasn't possible to putatively confirm the reasonable shipment of the innovative therapy prescribed

    • it wasn't possible to putatively confirm the reasonable shipment of conventional therapy prescribed (background therapy)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Careggi Hospital Firenze Italy
    2 Fondazione Policlinico Universitario A. Gemelli IRCCS. Roma Italy

    Sponsors and Collaborators

    • University of Messina
    • Campisi Mariapaola

    Investigators

    • Principal Investigator: Gianluca Di Bella, MD, University of Messina, Italy

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gianluca Di Bella, Associate Professor Cardiovascular Diseases, University of Messina
    ClinicalTrials.gov Identifier:
    NCT04387344
    Other Study ID Numbers:
    • UNIME_CARD_2
    First Posted:
    May 13, 2020
    Last Update Posted:
    May 13, 2020
    Last Verified:
    May 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 13, 2020