Evidence map›Paper›PMID 41906617›Full record

ArticleJACC. Advances2026

Diagnostic, Therapeutic, and Prognostic Implications of Carpal Tunnel Syndrome and Spinal Stenosis in Wild-type ATTR-Cardiomyopathy.

Philippe Debonnaire, Karl Dujardin, Erwan Donal, Nicolas Verheyen, Matthias Dupont, Delphine Vervloet, Philippe Timmermans, Anne-Catherine Pouleur, Steven Droogmans, Victor Sarli Issa and 20 more

Abstract read
In one paragraph

Article in JACC. Advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

30 authors.

Philippe DebonnaireCardiology Department, AZ Sint-Jan Brugge, Bruges, Belgium. Electronic address: philippe.debonnaire@azsintjan.be.
Karl DujardinCardiology Department, AZ Delta, Roeselare, Belgium.
Erwan DonalCardiology Department, CHU Rennes, Rennes, France.
Nicolas VerheyenCardiology Department, Medical University Graz, Graz, Austria.
Matthias DupontCardiology Department, Ziekenhuis Oost-Limburg, Genk, Belgium.
Delphine VervloetCardiology Department, Ziekenhuis Maria Middelares, Gent, Belgium.
Philippe TimmermansCardiology Department, Jessa Ziekenhuis, Hasselt, Belgium.
Anne-Catherine PouleurCardiology Department, Cliniques Universitaires St. Luc, Brussels, Belgium.
Steven DroogmansUniversitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Centrum voor Hart- en Vaatziekten, Jette, Belgium.
Victor Sarli IssaCardiology Department, Universitair Ziekenhuis Antwerpen, Edegem, Belgium.
Raluca DulgheruCardiology Department, CHU Sart-Tilman, Liège, Belgium.
Ruxandra JurcutEmergency Institute for Cardiovascular Diseases "Prof. Dr. C.C. Iliescu", Expert Center for Genetic Cardiovascular Diseases, Univeristy of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.
Madelien RegeerDepartment of Cardiology, Leiden University Medical Centre, Leiden, The Netherlands.
Antoine BondueDepartment of Cardiology, Hopital Erasme and IRIBHM, Université Libre de Bruxelles, Brussels, Belgium.
Emma ChristiaenCardiology Department, AZ Sint-Jan Brugge, Bruges, Belgium.
Wouter L'HoyesCardiology Department, AZ Sint-Jan Brugge, Bruges, Belgium.
Nicolas WyseureCardiology Department, AZ Delta, Roeselare, Belgium.
Mélanie BezardCardiology Department, CHU Rennes, Rennes, France.
David ZachCardiology Department, Medical University Graz, Graz, Austria.
Nora SchwegelCardiology Department, Medical University Graz, Graz, Austria.
Robbe KnapenCardiology Department, Jessa Ziekenhuis, Hasselt, Belgium.
Lars BuytaertUniversitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Centrum voor Hart- en Vaatziekten, Jette, Belgium.
Nils de MarneffeCardiology Department, CHU Sart-Tilman, Liège, Belgium.
Robert AdamEmergency Institute for Cardiovascular Diseases "Prof. Dr. C.C. Iliescu", Expert Center for Genetic Cardiovascular Diseases, Univeristy of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.
Nina Ajmone MarsanDepartment of Cardiology, Leiden University Medical Centre, Leiden, The Netherlands.
Francis BonteOrthopaedic Surgery Department, AZ Sint-Jan Brugge, Bruges, Belgium.
Nikolaas VantommeNeurosurgery Department, AZ Sint-Jan Brugge, Bruges, Belgium.
Ian BuysschaertCardiology Department, AZ Sint-Jan Brugge, Bruges, Belgium.
René TavernierCardiology Department, AZ Sint-Jan Brugge, Bruges, Belgium.
Sander TrensonCardiology Department, AZ Sint-Jan Brugge, Bruges, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn wild-type transthyretin cardiac amyloidosis (ATTRwt-CM), the prognostic role of carpal tunnel syndrome (CTS) is unclear and that of lumbar spinal stenosis (SS) remains unexplored.

objectivesThe aim was to examine the diagnostic, therapeutic, and prognostic relevance of bilateral CTS and SS in ATTRwt-CM, in relation to the tafamidis treatment.

methodsClinical characteristics of 1,449 patients with ATTRwt-CM were evaluated in a multicenter cohort. The primary endpoint was all-cause mortality. Cox multivariable regression was used to assess mortality in patients with and without CTS and SS.

resultsPreceding an ATTRwt-CM diagnosis, CTS and SS were present in 29% and 22% of patients, respectively, without sex-difference. CTS (P < 0.001), but not SS, was more prevalent among younger patients. Tenosynovial red flags and ATTRwt-CM diagnosis occurred approximately 4 years later in females vs males, with similar preceding time, suggesting later female ATTRwt-CM disease onset. Patients with vs without CTS and SS had lower National Amyloidosis Centre disease stage (P ≤ 0.001), despite similar symptomatic status. During a mean follow-up of 2.3 ± 1.8 years, 73% (1,052/1,449) of patients were initiated on tafamidis and 28% (406) died. Tafamidis was initiated more in CTS positive vs negative patients (78% vs 71%; P = 0.008), on average 2.3 years earlier (P < 0.001). More SS positive than negative patients received tafamidis (78% vs 71%; P = 0.018), but at similar age (P = 0.394). CTS (HR: 0.70; 95% CI: 0.52-0.95) and SS (HR: 0.68; 95% CI: 0.48-0.97) predicted lower mortality.

conclusionsBoth CTS and SS not only enable early ATTRwt-CM diagnosis and treatment initiation, but independently relate to improved survival, potentiating a role for opportunistic screening.

Indexed as

cardiac amyloidosiscarpal tunnel syndromemortalityspinal stenosistafamidistransthyretin

Identifiers

PMID41906617
PMCPMC13352003

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