Evidence map›Paper›PMID 39407234›Full record

ArticleOrphanet journal of rare diseases2024

A series of cases of transthyretin amyloid cardiomyopathy with negative bone scintigraphy but a confirmed positive endomyocardial biopsy.

Antoine Fraix, Emmanuel Itti, Amira Zaroui, Mounira Kharoubi, Elsa Poullot, Lionel Lerman, Soulef Guendouz, Olivier Huttin, Thibaud Damy, Arnault Galat

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Present and future of endomyocardial biopsy in cardiac amyloidosis.European heart journal supplements : journal of the European Society of Cardiology · 2025
    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

10 authors.

Antoine FraixCardiology Department, Institut Lorrain du Cœur et des Vaisseaux, Nancy University Medical Center, 54000, Nancy, France. antoine.fraix@gmail.com.ORCID 0000-0002-9932-2274
Emmanuel IttiAP-HP (Assistance Publique-Hôpitaux de Paris), Nuclear Medicine Department, Henri Mondor University Medical Center, 51 Avenue du Maréchal de Lattre de Tassigny, 94010, Créteil, France.
Amira ZarouiAP-HP (Assistance Publique-Hôpitaux de Paris), Cardiology Department, Henri Mondor University Medical Center, 51 Avenue du Maréchal de Lattre de Tassigny, 94010, Créteil, France.
Mounira KharoubiAP-HP (Assistance Publique-Hôpitaux de Paris), Cardiology Department, Henri Mondor University Medical Center, 51 Avenue du Maréchal de Lattre de Tassigny, 94010, Créteil, France.
Elsa PoullotAP-HP (Assistance Publique-Hôpitaux de Paris), French National Reference Center for Cardiac Amyloidosis, Cardiogen Network, Henri Mondor University Medical Center, 51 Avenue du Maréchal de Lattre de Tassigny, 94010, Créteil, France.
Lionel LermanAP-HP (Assistance Publique-Hôpitaux de Paris), Nuclear Medicine Department, Henri Mondor University Medical Center, 51 Avenue du Maréchal de Lattre de Tassigny, 94010, Créteil, France.
Soulef GuendouzAP-HP (Assistance Publique-Hôpitaux de Paris), Cardiology Department, Henri Mondor University Medical Center, 51 Avenue du Maréchal de Lattre de Tassigny, 94010, Créteil, France.
Olivier HuttinCardiology Department, Institut Lorrain du Cœur et des Vaisseaux, Nancy University Medical Center, 54000, Nancy, France.
Thibaud DamyAP-HP (Assistance Publique-Hôpitaux de Paris), Cardiology Department, Henri Mondor University Medical Center, 51 Avenue du Maréchal de Lattre de Tassigny, 94010, Créteil, France.
Arnault GalatAP-HP (Assistance Publique-Hôpitaux de Paris), Cardiology Department, Henri Mondor University Medical Center, 51 Avenue du Maréchal de Lattre de Tassigny, 94010, Créteil, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBone scintigraphy (BS) is established as an accurate, non-invasive method for the diagnosis of transthyretin amyloid cardiomyopathy (ATTR-CM). In a real-life setting, however, some patients with no cardiac uptake on BS turn out to have cardiac-biopsy-confirmed ATTR-CM. We retrospectively included all patients diagnosed at the French Referral Center for ATTR-CM and who had data for BS and a cardiac biopsy.

resultsOf 271 patients with positive cardiac biopsy, 14 (5%) had no cardiac uptake on

conclusionsAn endomyocardial biopsy may be necessary for confirming the diagnosis of ATTR-CM in patients with clinical and imaging signs of cardiac amyloidosis but no cardiac radiotracer uptake in BS.

Indexed as

Amyloid Neuropathies, FamilialCardiomyopathiesRadionuclide ImagingAgedAged, 80 and overBiopsyBone and BonesFemaleHumansMaleMiddle AgedMyocardiumPrealbuminRetrospective StudiesPrealbuminBiopsyCase seriesMutationNegative bone scintigraphyTransthyretin amyloid cardiomyopathy

Identifiers

PMID39407234
PMCPMC11481466

What OpenQuestion holds

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Registered trials

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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.