Evidence map›Paper›PMID 41337714›Full record

ReviewArchivos de cardiologia de Mexico2025

[Terapias dirigidas en amiloidosis cardíaca por transtiretina: una revisión del contexto clínico contemporáneo].

Juan P Costabel, Lucas L Suárez, M Cecilia Escalante-Seyffert, Juan D López-Ponce de León, Fabio Fernándes, Enrique A Berrios-Bárcenas

Abstract readReviewEnglish Abstract
In one paragraph

Review in Archivos de cardiologia de Mexico, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Juan P CostabelDepartamento de Cardiología, Instituto Cardiovascular de Buenos Aires, Buenos Aires, Argentina.
Lucas L SuárezDepartamento de Cardiología, Instituto Cardiovascular de Buenos Aires, Buenos Aires, Argentina.
M Cecilia Escalante-SeyffertClínica de Miocardiopatías, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
Juan D López-Ponce de LeónFundación Valle del Lili, Centro de Investigaciones Clínicas, Cali, Colombia.
Fabio FernándesUnidade Clínica de Cardiopatias Familiares, Instituto do Coração (InCor), Hospital das Clínicas, São Paulo, Brasil.
Enrique A Berrios-BárcenasClínica de Miocardiopatías, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transthyretin cardiac amyloidosis is a recently recognized disease, still significantly underdiagnosed. It is characterized by infiltration of amyloid proteins resulting from the destabilization of the transthyretin protein produced in the liver. There are two predominant presentations, the hereditary form and the wild-type form, both with cardiac involvement leading to heart failure and reducing life expectancy. In recent years, multiple treatment options targeting the cause of the disease, known as disease-modifying therapies, have emerged, and the use of traditional heart failure treatments has become necessary. This review addresses traditional and disease-modifying therapies for this disease, addressing their mechanisms of action, efficacy, safety, and real-world implementation.

Indexed as

Amyloid Neuropathies, FamilialCardiomyopathiesMolecular Targeted TherapyHumansCardiomyopathiesHereditary transthyretin-related amyloidosisTime to treatmentTransthyretin amyloidosisTreatment

Identifiers

PMID41337714
PMCPMC13035430

What OpenQuestion holds

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Registered trials

None linked

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.