Evidence map›Paper›PMID 40613025›Full record

ArticleCureus2025

A Challenging Case of Wild-Type Transthyretin Amyloidosis (ATTR) Amyloidosis Treated With Cardiac Resynchronization Therapy.

Hiroki Bansho, Daisuke Tomioka, Toru Geshi, Hiroshi Sakai, Yoshihisa Nakagawa

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

5 authors.

Hiroki BanshoCardiology, Shiga University of Medical Science, Otsu, JPN.
Daisuke TomiokaCardiology, Shiga University of Medical Science, Otsu, JPN.
Toru GeshiCardiology, Hikone Municipal Hospital, Hikone, JPN.
Hiroshi SakaiCardiology, Shiga University of Medical Science, Otsu, JPN.
Yoshihisa NakagawaCardiology, Shiga University of Medical Science, Otsu, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wild-type transthyretin amyloidosis (ATTRwt) is an age-associated systemic disorder characterized by extracellular deposition of misfolded transthyretin amyloid fibrils, leading to progressive organ dysfunction. Cardiac involvement is common and may result in restrictive cardiomyopathy, arrhythmias, and conduction disturbances, including left bundle branch block (LBBB). Although pharmacological therapy with transthyretin stabilizers, such as tafamidis, has been shown to reduce mortality in patients with ATTRwt cardiac amyloidosis (ATTRwt-CA), the role of device-based therapies, such as cardiac resynchronization therapy (CRT), remains controversial, particularly in patients with coexisting conduction abnormalities. We report the case of an 81-year-old woman diagnosed with ATTRwt-CA who presented with symptomatic heart failure and LBBB. Tafamidis therapy was initiated to improve her exercise tolerance and to reduce her risk of mortality. Owing to the presence of LBBB and evidence of mechanical dyssynchrony, CRT was also introduced in an effort to prevent the deterioration of her heart failure with reduced ejection fraction. Device optimization was guided by gated myocardial perfusion imaging, performed using single photon emission computed tomography (SPECT), which enabled a detailed assessment of her left ventricular synchrony and informed CRT programming. Following CRT implantation and optimization, the patient exhibited marked symptomatic improvement, including resolution of her exertional dyspnea and fatigue. Objective assessments demonstrated improved left ventricular contractility and reverse remodeling, suggesting a favorable response to CRT. This case underscores the potential value of CRT in selected patients with ATTRwt-CA and conduction system disease, particularly when mechanical dyssynchrony is evident. Furthermore, it highlights the utility of nuclear imaging modalities such as SPECT in guiding CRT optimization in this unique patient population. Prospective studies are warranted to better define the indications, predictors of response, and long-term outcomes of CRT in patients with ATTRwt-CA.

Indexed as

cardiac resynchronization therapyheart failureleft bundle branch blockreduced ejection fractionwild-type attr amyloidosis

Identifiers

PMID40613025
PMCPMC12223460

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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.