Incremental prognostic utility of congestion markers in cardiac transthyretin amyloidosis.

ATTR amyloidosis Cardiac amyloidosis Congestion Diuretics NT-proBNP Risk stratification Tricuspid regurgitation peak velocity (tr-vmax)

Journal

Clinical research in cardiology : official journal of the German Cardiac Society
ISSN: 1861-0692
Titre abrégé: Clin Res Cardiol
Pays: Germany
ID NLM: 101264123

Informations de publication

Date de publication:
06 Aug 2024
Historique:
received: 05 06 2024
accepted: 29 07 2024
medline: 6 8 2024
pubmed: 6 8 2024
entrez: 6 8 2024
Statut: aheadofprint

Résumé

Congestion is prognostically relevant in cardiac transthyretin amyloidosis (ATTR-CA), but whether congestion has an incremental prognostic value beyond the well-established, congestion-sensitive NT-proBNP is unknown. Therefore, we aimed to comparatively evaluate the prognostic utility of several congestion surrogates over NT-proBNP. We estimated hazard ratios by Cox proportional hazards regressions with time-varying covariates from a panel data set of the local amyloidosis cohort study AmyKoS. Different models were compared by using chi(χ) 131 ATTR-CA patients (wild-type 84.0%, hereditary 6.9%, without genetic testing 9.2%; median age 78.7 (quartiles 73.3, 82.1) years; 85.5% male) with 566 observations across a median follow-up of 38.2 (30.6; 48.2) months were analyzed. 83.2% received disease-modifying treatment; 20.6% participated concurrently in placebo-controlled gene silencer trials. Information on congestion improved biomarker-driven risk stratification and identified patients at the highest risk. Echocardiographic congestion markers performed better than clinical findings and daily diuretic use/dosage. Relevant adjusters were daily diuretic dosage, disease-modifying treatment, eGFR, and right atrial volume. NT-proBNP and the tricuspid regurgitation peak velocity (tr-v

Sections du résumé

BACKGROUND/AIMS OBJECTIVE
Congestion is prognostically relevant in cardiac transthyretin amyloidosis (ATTR-CA), but whether congestion has an incremental prognostic value beyond the well-established, congestion-sensitive NT-proBNP is unknown. Therefore, we aimed to comparatively evaluate the prognostic utility of several congestion surrogates over NT-proBNP.
METHODS METHODS
We estimated hazard ratios by Cox proportional hazards regressions with time-varying covariates from a panel data set of the local amyloidosis cohort study AmyKoS. Different models were compared by using chi(χ)
RESULTS/CONCLUSION CONCLUSIONS
131 ATTR-CA patients (wild-type 84.0%, hereditary 6.9%, without genetic testing 9.2%; median age 78.7 (quartiles 73.3, 82.1) years; 85.5% male) with 566 observations across a median follow-up of 38.2 (30.6; 48.2) months were analyzed. 83.2% received disease-modifying treatment; 20.6% participated concurrently in placebo-controlled gene silencer trials. Information on congestion improved biomarker-driven risk stratification and identified patients at the highest risk. Echocardiographic congestion markers performed better than clinical findings and daily diuretic use/dosage. Relevant adjusters were daily diuretic dosage, disease-modifying treatment, eGFR, and right atrial volume. NT-proBNP and the tricuspid regurgitation peak velocity (tr-v

Identifiants

pubmed: 39105788
doi: 10.1007/s00392-024-02512-4
pii: 10.1007/s00392-024-02512-4
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Interdisziplinäres Zentrum für Klinische Forschung, Universitätsklinikum Würzburg
ID : Z-2_CSP-08

Informations de copyright

© 2024. Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Sandra Michaela Ihne-Schubert (SM)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany. ihne_s@ukw.de.
Department of Internal Medicine II, Hematology, University Hospital of Würzburg, Würzburg, Germany. ihne_s@ukw.de.
Department of Internal Medicine IV, University Hospital Gießen and Marburg, Gießen, Germany. ihne_s@ukw.de.
CIRCLE - Centre for Innovation Research, Lund University, Lund, Sweden. ihne_s@ukw.de.

Caroline Morbach (C)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department Clinical Research & Epidemiology, Comprehensive Heart Failure Center, University and University Hospital of Würzburg, Würzburg, Germany.
Department of Internal Medicine I, Cardiology, University Hospital of Würzburg, Würzburg, Germany.

Vladimir Cejka (V)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department Clinical Research & Epidemiology, Comprehensive Heart Failure Center, University and University Hospital of Würzburg, Würzburg, Germany.
Department of Internal Medicine I, Cardiology, University Hospital of Würzburg, Würzburg, Germany.

Maximilian Johannes Steinhardt (MJ)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department of Internal Medicine II, Hematology, University Hospital of Würzburg, Würzburg, Germany.

Aikaterini Papagianni (A)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department of Neurology, University Hospital of Würzburg, Würzburg, Germany.

Stefan Frantz (S)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department Clinical Research & Epidemiology, Comprehensive Heart Failure Center, University and University Hospital of Würzburg, Würzburg, Germany.
Department of Internal Medicine I, Cardiology, University Hospital of Würzburg, Würzburg, Germany.

Hermann Einsele (H)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department of Internal Medicine II, Hematology, University Hospital of Würzburg, Würzburg, Germany.

Thomas Wehler (T)

Department of Internal Medicine IV, University Hospital Gießen and Marburg, Gießen, Germany.

Klaus Martin Kortüm (KM)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department of Internal Medicine II, Hematology, University Hospital of Würzburg, Würzburg, Germany.

Claudia Sommer (C)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department of Neurology, University Hospital of Würzburg, Würzburg, Germany.

Stefan Störk (S)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department Clinical Research & Epidemiology, Comprehensive Heart Failure Center, University and University Hospital of Würzburg, Würzburg, Germany.
Department of Internal Medicine I, Cardiology, University Hospital of Würzburg, Würzburg, Germany.

Torben Schubert (T)

CIRCLE - Centre for Innovation Research, Lund University, Lund, Sweden.
Fraunhofer Institute for Systems and Innovation Research ISI, Karlsruhe, Germany.
Department of Design Science (LTH), Lund University, Lund, Sweden.

Andreas Geier (A)

Interdisciplinary Amyloidosis Center of Northern Bavaria, University Hospital of Würzburg, Würzburg, Germany.
Department of Internal Medicine II, Hepatology, University Hospital of Würzburg, Würzburg, Germany.

Classifications MeSH