Evidence map›Paper›PMID 41680282›Full record

ArticleScientific reports2026

Prognostic value of right ventricular-pulmonary artery coupling in patients with muscular dystrophies.

Abdallah Fayssoil, Nicolas Mansencal, Cendrine Chaffaut, Karim Wahbi, Frederic Lofaso, Helene Prigent, David Orlikowski, Bernard Clair, Pascal Laforet, Guillaume Bassez and 8 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

18 authors.

Abdallah FayssoilDepartment of Cardiology, Centre de référence des cardiomyopathies et des troubles du rythme cardiaque héréditaires ou rares, Ambroise Paré Hospital, Assistance Publique- Hôpitaux de Paris (AP-HP), Université de Versailles-Saint Quentin (UVSQ), Boulogne-Billancourt, France. abdallah.fayssoil@aphp.fr.
Nicolas MansencalDepartment of Cardiology, Centre de référence des cardiomyopathies et des troubles du rythme cardiaque héréditaires ou rares, Ambroise Paré Hospital, Assistance Publique- Hôpitaux de Paris (AP-HP), Université de Versailles-Saint Quentin (UVSQ), Boulogne-Billancourt, France.
Cendrine ChaffautSBIM, Saint Louis Hospital, Paris, France.
Karim WahbiDepartment of Cardiology, Cochin Hospital, APHP, Paris, France.
Frederic LofasoDepartment of Physiology, Raymond Poincaré Hospital, APHP, Garches, France.
Helene PrigentDepartment of Physiology, Raymond Poincaré Hospital, APHP, Garches, France.
David OrlikowskiIntensive Care Unit, Raymond Poincaré Hospital, APHP, Garches, France.
Bernard ClairIntensive Care Unit, Raymond Poincaré Hospital, APHP, Garches, France.
Pascal LaforetDepartment of Neurology, Raymond Poincaré Hospital, APHP, Garches, France.
Guillaume BassezMyology Institute, Pitié Salpetrière Hospital, Paris, France.
Anthony BehinMyology Institute, Pitié Salpetrière Hospital, Paris, France.
Bertrand FontaineMyology Institute, Pitié Salpetrière Hospital, Paris, France.
Henri -Marc BecaneMyology Institute, Pitié Salpetrière Hospital, Paris, France.
Denis DubocDepartment of Cardiology, Cochin Hospital, APHP, Paris, France.
Olivier DubourgDepartment of Cardiology, Centre de référence des cardiomyopathies et des troubles du rythme cardiaque héréditaires ou rares, Ambroise Paré Hospital, Assistance Publique- Hôpitaux de Paris (AP-HP), Université de Versailles-Saint Quentin (UVSQ), Boulogne-Billancourt, France.
Sylvie ChevretSBIM, Saint Louis Hospital, Paris, France.
Djillali AnnaneIntensive Care Unit, Raymond Poincaré Hospital, APHP, Garches, France.
Tanya StojkovicMyology Institute, Pitié Salpetrière Hospital, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Muscular dystrophies can affect the heart and the respiratory system. Right ventricular‒pulmonary artery (RV‒PA) coupling may reflect right ventricular adaptation to respiratory status. Since RV function is very sensitive to afterload, evaluating RV function coupled with pulmonary circulation is more relevant for assessing clinical issues in patients. The aim of this study was to assess the prognostic value of the tricuspid annular plane systolic excursion/systolic pulmonary artery pressure (TAPSE/sPAP), an index of RV–PA coupling, in patients with Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD) and sarcoglycanopathies. The study included retrospectively, from 2015 to 2023, patients with DMD, BMD and sarcoglycanopathies, who were followed in Pitié-Salpêtrière Hospital and Raymond-Poincaré Hospital (France) and who benefited from echocardiography that included a measurement of TAPSE/sPAP. The primary goal was to assess the prognostic value of the TAPSE/sPAP in terms of predicting cardiac events. The study included 113 patients (median age 28 years): DMD (n = 60, 53%), BMD (n = 33, 29%) and sarcoglycanopathies (n = 20, 18%). Home mechanical ventilation was present in 51 patients (46%), and 69% of the patients were wheelchair bound. Left ventricular systolic dysfunction (LVEF < 50%) was present in 37% of the patients. The median sPAP was 22 mmHg [19–27], whereas the median TAPSE was 16 mm [13–18]. Using a Cox model, we found that the TAPSE/sPAP*10 was significantly associated with cardiac events; the higher the TAPSE/sPAP, the better was the outcome (HR 0.33, 95% CI [0.16–0.69], p 0.003). According to the Youden criterion, the cutoff TAPSE/sPAP*10 was 5.3 mm/mmHg. RV–PA coupling, defined by the TAPSE/sPAP, may be a prognostic biomarker in patients with muscular dystrophies.

Indexed as

Heart VentriclesMuscular DystrophiesPulmonary ArteryVentricular Function, RightAdolescentAdultEchocardiographyFemaleHumansMaleMuscular Dystrophy, DuchennePrognosisRetrospective StudiesYoung AdultBecker muscular dystrophyDuchenne muscular dystrophyEchocardiographyPrognosisRight ventriculopulmonary artery couplingSarcoglycanopathy

Identifiers

PMID41680282
PMCPMC12976063

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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.