Evidence map›Paper›PMID 41220156›Full record

Observational studyJournal of the American Heart Association2025

Cardiac Resynchronization Therapy, Remodeling, and Outcome in Patients With Amyloid Transthyretin Cardiomyopathy.

Alberto Aimo, Martina Nesti, Giuseppe Vergaro, Ammar M Killu, Dimitrios Bampatsias, Daniela Tomasoni, Cinzia Forleo, Francesco Musca, Matteo Serenelli, Julie Rosenthal and 27 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

37 authors.

Alberto AimoScuola Superiore Sant'Anna Pisa Italy.ORCID 0000-0001-9129-9519
Martina NestiFondazione Toscana Gabriele Monasterio Pisa Italy.ORCID 0000-0001-8995-3884
Giuseppe VergaroScuola Superiore Sant'Anna Pisa Italy.ORCID 0000-0002-7066-6006
Ammar M KilluMayo Clinic Rochester MN USA.ORCID 0000-0002-5525-1806
Dimitrios BampatsiasColumbia University New York City NY USA.
Daniela TomasoniASST Spedali Civili di Brescia and University of Brescia Italy.ORCID 0000-0002-7584-2857
Cinzia ForleoUniversity Hospital of Bari Italy.ORCID 0000-0002-9452-4037
Francesco MuscaNiguarda Hospital Milan Italy.ORCID 0000-0002-3968-4759
Matteo SerenelliUniversity of Ferrara Italy.
Julie RosenthalMayo Clinic Hospital Phoenix AZ USA.ORCID 0000-0001-7002-9595
Sergio L TeruyaColumbia University New York City NY USA.ORCID 0000-0002-4653-9330
Nader J Al-ShakarchiMayo Clinic Rochester MN USA.ORCID 0000-0003-1496-8103
Mariel S TamezeFondazione Toscana Gabriele Monasterio Pisa Italy.
Vincenzo CastiglioneScuola Superiore Sant'Anna Pisa Italy.ORCID 0000-0002-9285-2328
Alessio NicolaiASST Spedali Civili di Brescia and University of Brescia Italy.
Giorgia PanichellaTuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy.
Riccardo SaroEuropean Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart Amsterdam the Netherlands.
Aldostefano PorcariEuropean Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart Amsterdam the Netherlands.ORCID 0000-0003-3307-0825
Giulio SinigianiUniversity of Padua Italy.
Vera FicoTuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy.ORCID 0009-0006-6149-7278
Elisa FrauTuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy.
Reem MatarMayo Clinic Rochester MN USA.
Andrea I GuaricciUniversity Hospital of Bari Italy.ORCID 0000-0001-7133-4401
Giacomo TiniDepartment of Clinical and Molecular Medicine Sapienza University of Rome Italy.ORCID 0000-0001-8520-152X
Alberto CiprianiUniversity of Padua Italy.ORCID 0000-0001-7842-6202
Maria B MusumeciDepartment of Clinical and Molecular Medicine Sapienza University of Rome Italy.
Simone LonghiSt. Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna Italy.ORCID 0000-0002-7512-1179
Cristina ChimentiUmberto I Hospital Rome Italy.ORCID 0000-0001-5954-3796
Marco MetraASST Spedali Civili di Brescia and University of Brescia Italy.ORCID 0000-0001-6691-8568
Martha GroganMayo Clinic Rochester MN USA.ORCID 0000-0002-2541-4440
Federico PerfettoTuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy.ORCID 0000-0003-0276-8331
Francesco CappelliTuscan Regional Amyloidosis Centre Careggi University Hospital Florence Italy.ORCID 0000-0002-1622-0732
Marco MerloEuropean Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart Amsterdam the Netherlands.ORCID 0000-0002-1022-3131
Gianfranco SinagraEuropean Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart Amsterdam the Netherlands.ORCID 0000-0003-2700-8478
Mathew S MaurerColumbia University New York City NY USA.ORCID 0000-0001-5400-5008
Ahmad MasriOregon Health and Science University Medical Group Portland OR USA.ORCID 0000-0002-6390-6526
Michele EmdinScuola Superiore Sant'Anna Pisa Italy.ORCID 0000-0002-8541-1962

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransthyretin amyloid cardiomyopathy (ATTR-CM) has a specific pathophysiology, with myocardial stiffening and systolic dysfunction only in advanced stages. We aimed to investigate the response to cardiac resynchronization therapy (CRT) in ATTR-CM compared with heart failure.

methodsIn this multicenter, observational study, patients with ATTR-CM receiving CRT (n=101) were matched to patients without amyloid cardiomyopathy by sex, age, and implantation type (CRT with versus without defibrillator versus conduction system pacing, upgrade versus first implant). We evaluated changes in QRS duration and echocardiographic parameters following CRT implantation and at the most recent available assessments. The study end points were all-cause death alone or combined with heart failure hospitalization.

resultsPatients with ATTR-CM (median age, 76 [interquartile range, 72-83] years, 98% men, left ventricular (LV) ejection fraction 30% [26-33]) showed greater QRS shortening after CRT implantation (

conclusionsFollowing CRT implantation, patients with ATTR-CM show QRS narrowing and improvement in LV ejection fraction, not different from patients without amyloid cardiomyopathy. Early favorable LV remodeling seems to be associated with a lower risk of all-cause death.

Indexed as

Amyloid Neuropathies, FamilialCardiac Resynchronization TherapyCardiomyopathiesHeart FailureVentricular Function, LeftVentricular RemodelingAgedAged, 80 and overEchocardiographyElectrocardiographyFemaleHumansMaleStroke VolumeTime FactorsTreatment Outcomecardiac amyloidosiscardiac resynchronization therapyconduction system pacingCRToutcomeremodelingtransthyretin

Identifiers

PMID41220156
PMCPMC12887198

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.