Evidence map›Paper›PMID 41116186›Full record

ArticleOrphanet journal of rare diseases2025

Progression of QRS duration - a potential surrogate marker of survival in ATTRwt amyloidosis patients.

Selina Hein, Fabian Aus dem Siepen, Sonja M Zierleyn, Maximilian Knoll, Hugo A Katus, Norbert Frey, Arnt V Kristen

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Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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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

7 authors.

Selina HeinDepartment of Cardiology, Angiology and Pulmonology, University Hospital Heidelberg, Heidelberg, Germany. selina.hein@web.de.ORCID 0000-0003-0139-4200
Fabian Aus dem SiepenDepartment of Cardiology, Angiology and Pulmonology, University Hospital Heidelberg, Heidelberg, Germany.
Sonja M ZierleynDepartment of Cardiology, Angiology and Pulmonology, University Hospital Heidelberg, Heidelberg, Germany.
Maximilian KnollDepartment of Radiation Oncology, Heidelberg Ion-Beam Therapy Center (HIT), Heidelberg University Hospital (UKHD), German Cancer Research Center, Heidelberg, Germany.
Hugo A KatusDepartment of Cardiology, Angiology and Pulmonology, University Hospital Heidelberg, Heidelberg, Germany.
Norbert FreyDepartment of Cardiology, Angiology and Pulmonology, University Hospital Heidelberg, Heidelberg, Germany.
Arnt V KristenDepartment of Cardiology, Angiology and Pulmonology, University Hospital Heidelberg, Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIn wild-type transthyretin amyloidosis (ATTRwt), the deposition of transthyretin in the myocardium leads to progressive heart failure. However, little is known about the short-term natural progression of this disease and potential predictors of outcome. OBJECTIVES &

methodsTherefore, this study longitudinally analyzed the clinical findings (ECG, echocardiography, and laboratory tests) of 65 patients suffering from ATTRwt at baseline and at follow-up visits after 12 months.

resultsIn total, 44 patients (67.7%) presented with abnormal ECGs, prolonged PR and QRS durations and low-voltage patterns. Pacemaker placement was performed in eleven patients (16.9%). At the one-year follow-up visit, we detected significant increases in the QRS duration (from 119.7 ± 4.0 to 125.9 ± 4.3 ms; p < 0.05), intraventricular septum thickness (from 18.9 ± 0.5 mm to 19.9 ± 0.5 mm; p < 0.05) and ejection fraction (EF) (from 45.4 ± 2.1% to 38.9 ± 2.6%; p < 0.05) compared with those at the baseline visit. During follow-up, 16 patients (24.6%) died. Predictors of worse outcomes were progression in QRS duration, low EF, reduced renal function, impaired right ventricular function and the need for pacemaker implantation.

conclusionsIn ATTRwt, precise evaluation via routine cardiac diagnosis helps to identify patients with an elevated risk of mortality. Patients with prolonged QRS duration, progressive myocardial hypertrophy, right ventricular failure, reduced renal function and the need for cardiac pacemakers are at increased risk for one-year mortality.

Indexed as

Amyloid Neuropathies, FamilialAgedDisease ProgressionEchocardiographyElectrocardiographyFemaleHumansMaleMiddle AgedRoutine careSurvivalTransthyretinWild-type ATTR amyloidosis

Identifiers

PMID41116186
PMCPMC12539068

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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.