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  3. Impact of tafamidis on myocardial function and CMR tissue characteristics in transthyretin amyloid cardiomyopathy.
 

Impact of tafamidis on myocardial function and CMR tissue characteristics in transthyretin amyloid cardiomyopathy.

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BORIS DOI
10.48350/196715
Date of Publication
October 2024
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Author
Dobner, Stephan
Universitätsklinik für Kardiologie
Bernhard, Benedikt
Universitätsklinik für Kardiologie
Ninck, Lorenz
Wieser, Monika
Universitätsklinik für Kardiologie
Bakula, Adam
Universitätsklinik für Kardiologie
Wahl, Andreas
Universitätsklinik für Kardiologie
Köchli, Valentin
Universitätsklinik für Kardiologie
Spano, Giancarlo
Universitätsklinik für Kardiologie
Boscolo Berto, Martina
Universitätsklinik für Kardiologie
Elchinova, Elena Georgieva
Universitätsklinik für Kardiologie
Safarkhanlo, Yasamanorcid-logo
Universitätsklinik für Kardiologie
Stortecky, Stefan
Universitätsklinik für Kardiologie
Schütze, Jonathan
Universitätsklinik für Kardiologie
Shiri Lord, Isaac
Universitätsklinik für Kardiologie
Hunziker Munsch, Lukas Christoph
Universitätsklinik für Kardiologie
Gräni, Christoph
Universitätsklinik für Kardiologie
Subject(s)

600 - Technology::610...

Series
ESC Heart Failure
ISSN or ISBN (if monograph)
2055-5822
Publisher
Wiley
Language
English
Publisher DOI
10.1002/ehf2.14815
PubMed ID
38736040
Uncontrolled Keywords

Cardiac amyloidosis C...

Description
AIMS

Tafamidis improves clinical outcomes in transthyretin amyloid cardiomyopathy (ATTR-CM), yet how tafamidis affects cardiac structure and function remains poorly described. This study prospectively analysed the effect of tafamidis on 12-month longitudinal changes in cardiac structure and function by cardiac magnetic resonance (CMR) compared with the natural course of disease in an untreated historic control cohort.

METHODS AND RESULTS

ATTR-CM patients underwent CMR at tafamidis initiation and at 12 months. Untreated patients with serial CMRs served as reference to compare biventricular function, global longitudinal strain (GLS), LV mass and extracellular volume fraction (ECV). Thirty-six tafamidis-treated (n = 35; 97.1% male) and 15 untreated patients (n = 14; 93.3% male) with a mean age of 78.3 ± 6.5 and 76.9 ± 6.5, respectively, and comparable baseline characteristics were included. Tafamidis was associated with preserving biventricular function (LVEF (%): 50.5 ± 12 to 50.7 ± 11.5, P = 0.87; RVEF (%): 48.2 ± 10.4 to 48.2 ± 9.4, P = 0.99) and LV-GLS (-9.6 ± 3.2 to -9.9 ± 2.4%; P = 0.595) at 12 months, while a significantly reduced RV-function (50.8 ± 7.3 to 44.2 ± 11.6%, P = 0.028; P (change over time between groups) = 0.032) and numerically worsening LVGLS (-10.9 ± 3.3 to -9.1 ± 2.9%, P = 0.097; P (change over time between groups) = 0.048) was observed without treatment. LV mass significantly declined with tafamidis (184.7 ± 47.7 to 176.5 ± 44.3 g; P = 0.011), yet remained unchanged in untreated patients (163.8 ± 47.5 to 171.2 ± 39.7 g P = 0.356, P (change over time between groups) = 0.027). Irrespective of tafamidis, ECV and native T1-mapping did not change significantly from baseline to 12-month follow-up (P > 0.05).

CONCLUSIONS

Compared with untreated ATTR-CM patients, initiation of tafamidis preserved CMR-measured biventricular function and reduced LV mass at 12 months. ECV and native T1-mapping did not change significantly comparable to baseline in both groups.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/177358
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ESC_Heart_Failure_-_2024_-_Dobner_-_Impact_of_tafamidis_on_myocardial_function_and_CMR_tissue_characteristics_in.pdftextAdobe PDF3.26 MBAttribution-NonCommercial (CC BY-NC 4.0)publishedOpen
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