Evidence map›Paper›PMID 37600055›Full record

ArticleFrontiers in cardiovascular medicine2023

Prognostic value of soluble ST2 in AL and TTR cardiac amyloidosis: a multicenter study.

Martin Nicol, Giuseppe Vergaro, Thibaud Damy, Mounira Kharoubi, Mathilde Baudet, Elena Sofia Canuti, Alberto Aimo, Vincenzo Castiglione, Michele Emdin, Bruno Royer and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 41% of its field
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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Article
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

14 authors at 7 institutions in 2 countries.

Martin NicolCardiology Department Lariboisière Saint Louis Hospital, University of Paris, Paris, France.
Giuseppe VergaroCardiology Department, Scuola Superiore Sant'Anna and Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Thibaud DamyReferral Cardiac Amyloidosis Center and Cardiology Department, Mondor Hospital, IMRB U955 and Université Paris Est Créteil all at 94000 Créteil, France.
Mounira KharoubiReferral Cardiac Amyloidosis Center and Cardiology Department, Mondor Hospital, IMRB U955 and Université Paris Est Créteil all at 94000 Créteil, France.
Mathilde BaudetCardiology Department Lariboisière Saint Louis Hospital, University of Paris, Paris, France.
Elena Sofia CanutiSapienza Universita di Roma, Universita di Bologna, Roma, Italy.
Alberto AimoCardiology Department, Scuola Superiore Sant'Anna and Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Vincenzo CastiglioneCardiology Department, Scuola Superiore Sant'Anna and Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Michele EmdinCardiology Department, Scuola Superiore Sant'Anna and Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Bruno RoyerImmuno-Hematology Department, Saint Louis Hospital, University of Paris, Paris, France.
Stephanie HarelImmuno-Hematology Department, Saint Louis Hospital, University of Paris, Paris, France.
Alain Cohen-SolalCardiology Department Lariboisière Saint Louis Hospital, University of Paris, Paris, France.
Bertrand ArnulfImmuno-Hematology Department, Saint Louis Hospital, University of Paris, Paris, France.
Damien LogeartCardiology Department Lariboisière Saint Louis Hospital, University of Paris, Paris, France.
Université Paris Cité · FRScuola Superiore Sant'Anna · ITHôpital Saint-Louis · FRUniversité Paris-Est Créteil · FRFondazione Toscana Gabriele Monasterio · ITHôpital Lariboisière · FRSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Both light-chain (AL) amyloidosis and transthyretin (ATTR) amyloidosis are types of cardiac amyloidosis (CA) that require accurate prognostic stratification to plan therapeutic strategies and follow-ups. Cardiac biomarkers, e.g., N-terminal pro-B-type natriuretic peptide (NT-proBNP) and high-sensitivity cardiac troponin T (Hs-cTnT), remain the cornerstone of the prognostic assessment. An increased level of soluble suppression of tumorigenesis-2 (sST2) is predictive of adverse events [all-cause death and heart failure (HF) hospitalizations] in patients with HF. This study aimed to evaluate the prognostic value of circulating sST2 levels in AL-CA and ATTR-CA. Methods: We carried out a multicenter study including 133 patients with AL-CA and 152 patients with ATTR-CA. During an elective outpatient visit for the diagnosis of CA, Mayo Clinic staging [NT-proBNP, Hs-cTnT, differential of free light chains (DFLCs)] and sST2 were assessed for all AL patients. Gillmore staging [including estimated glomerular filtration rate (eGFR), NT-proBNP] and Grogan staging (including NT-proBNP and Hs-cTnT) were assessed for TTR-CA patients. Results: The median age was 73 years [interquartile range (IQR) 61-81], and 53% were men. The endpoint was the composite of all-cause death or first HF-related hospitalization. The median follow-up was 20 months (IQR 3-34) in AL amyloidosis and 33 months (6-45) in TTR amyloidosis. The primary outcome occurred in 70 (53%) and 99 (65%) of AL and TTR patients, respectively. sST2 levels were higher in patients with AL-CA than in patients with ATTR-CA: 39 ng/L (26-80) vs. 32 ng/L (21-46), Conclusion: sST2 level is a relevant predictor of death and HF hospitalization in AL cardiac amyloidosis and adds prognostic stratification on top of NT-proBNP, Hs cTnT, and DFLC.

Indexed as

ALbiomarkercardiac amyloidosisprognosissST2TTR

Identifiers

PMID37600055
PMCPMC10433216
OpenAlexW4385493653

What Socratic holds

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LicenceCC BY
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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 Socratic graph.