Design and initiation of the Croatian Transthyretin Cardiac Amyloidosis Registry

    Authors

    Keywords

    registry, transthyretin amyloidosis, cardiomyopathy, outcomes

    DOI

    https://doi.org/10.15836/ccar2022.274

    Full Text

    Introduction: Transthyretin amyloidosis (ATTR) is a rare disease with heterogeneous symptoms and unfavorable outcomes unless diagnosed and treated in the early stage. Phenotypes and clinical presentations relate to underlying genetic variants (where genotype heterogeneity is well-known and related to endemic geographic regions) or the acquired form (wild type) ( 1 , 2 ). The Croatian Transthyretin Cardiac Amyloidosis (CroATTR) Registry is designed as a national, longitudinal, non-interventional, and both retrospective and prospective ATTR registry. Methods: We aim to include patients with clinically proven hATTR-CM or wtATTR-CM according to the current guidelines, or family members with confirmed mutation of the TTR gene (regardless of the presence of cardiomyopathy). The registry will acquire basic demographic characteristics and results of genetic testing (for hATTR), followed by clinical work-up capturing patient demographics, quality of life questionnaires, medical and family history, data from 12-lead electrocardiogram (ECG), echocardiography, cardiac magnetic resonance imaging (cMRI) (with an emphasis on typical ATTR red flags), 99mTc- pyrophosphate scintigraphy, electromyoneurography, and myocardial biopsy, as available. The registry will follow disease-specific outcomes: 1. overall survival, 2. cardiovascular mortality, 3. heart failure hospitalizations/unscheduled physician visits, 4. patient reported outcomes in the area of quality-of-life changes. The registry will also collect data on disease- specific treatments in our population: the proportion of patients treated with of guideline directed medical therapies (GDMT) for amyloidosis and heart and/or liver transplantation. The data will be captured at the time of inclusion of the patient in the registry (including retrospective data focusing on the time the diagnosis was first made) and will include prospective recurring visits. Data will be collected and managed using REDCap electronic data capture tools (the design of the database is shown on Figure 1 ). Croatian Transthyretin Cardiac Amyloidosis Registry Electronic Case Report Form. Conclusion: The CroATTR Registry will aggregate ATTR patients and allow further insights into the occurrence and natural course of disease. A particular emphasis will be made on the rare genetic mutation prevalent in our population, the utilization of guideline directed medical therapies and transplantation procedures.

    Cardiologia Croatica
    Back to search

    Design and initiation of the Croatian Transthyretin Cardiac Amyloidosis Registry

    Extended Abstract
    Issue9-10
    Published
    Pages274
    PDF via DOIhttps://doi.org/10.15836/ccar2022.274
    registry
    transthyretin amyloidosis
    cardiomyopathy
    outcomes

    Authors

    Ivo Planinc*ORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Dubravka ŠipušORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Filip LončarićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Nina JakušORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Dora FabijanovićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Marijan PašalićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Hrvoje JurinORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Jure SamardžićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Boško SkorićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Fran BorovečkiORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Davor MiličićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Maja ČikešORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia

    Full Text

    Introduction: Transthyretin amyloidosis (ATTR) is a rare disease with heterogeneous symptoms and unfavorable outcomes unless diagnosed and treated in the early stage. Phenotypes and clinical presentations relate to underlying genetic variants (where genotype heterogeneity is well-known and related to endemic geographic regions) or the acquired form (wild type) ( 1 , 2 ). The Croatian Transthyretin Cardiac Amyloidosis (CroATTR) Registry is designed as a national, longitudinal, non-interventional, and both retrospective and prospective ATTR registry. Methods: We aim to include patients with clinically proven hATTR-CM or wtATTR-CM according to the current guidelines, or family members with confirmed mutation of the TTR gene (regardless of the presence of cardiomyopathy). The registry will acquire basic demographic characteristics and results of genetic testing (for hATTR), followed by clinical work-up capturing patient demographics, quality of life questionnaires, medical and family history, data from 12-lead electrocardiogram (ECG), echocardiography, cardiac magnetic resonance imaging (cMRI) (with an emphasis on typical ATTR red flags), 99mTc- pyrophosphate scintigraphy, electromyoneurography, and myocardial biopsy, as available. The registry will follow disease-specific outcomes: 1. overall survival, 2. cardiovascular mortality, 3. heart failure hospitalizations/unscheduled physician visits, 4. patient reported outcomes in the area of quality-of-life changes. The registry will also collect data on disease- specific treatments in our population: the proportion of patients treated with of guideline directed medical therapies (GDMT) for amyloidosis and heart and/or liver transplantation. The data will be captured at the time of inclusion of the patient in the registry (including retrospective data focusing on the time the diagnosis was first made) and will include prospective recurring visits. Data will be collected and managed using REDCap electronic data capture tools (the design of the database is shown on Figure 1 ). Croatian Transthyretin Cardiac Amyloidosis Registry Electronic Case Report Form. Conclusion: The CroATTR Registry will aggregate ATTR patients and allow further insights into the occurrence and natural course of disease. A particular emphasis will be made on the rare genetic mutation prevalent in our population, the utilization of guideline directed medical therapies and transplantation procedures.