Evidence map›Paper›PMID 38759116›Full record

Observational studyRheumatology (Oxford, England)2024

Native myocardial T1 and right ventricular size by CMR predict outcome in systemic sclerosis-associated pulmonary hypertension.

Daniel S Knight, Ruta Virsinskaite, Nina Karia, Alice R Cole, Rory H Maclean, James T Brown, Rishi K Patel, Yousuf Razvi, Lucia Venneri, Tushar Kotecha and 9 more

Abstract readObservational Study
In one paragraph

Observational study in Rheumatology (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

19 authors.

Daniel S KnightNational Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust, London, UK.ORCID 0000-0002-0512-3961
Ruta VirsinskaiteNational Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust, London, UK.
Nina KariaNational Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust, London, UK.
Alice R ColeCentre for Rheumatology and Connective Tissue Diseases, UCL Medical School (Royal Free Campus), London, UK.
Rory H MacleanCentre for Rheumatology and Connective Tissue Diseases, UCL Medical School (Royal Free Campus), London, UK.
James T BrownNational Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust, London, UK.
Rishi K PatelDepartment of Cardiac MRI, Royal Free London NHS Foundation Trust, London, UK.ORCID 0000-0002-3177-5680
Yousuf RazviDepartment of Cardiac MRI, Royal Free London NHS Foundation Trust, London, UK.ORCID 0000-0003-4766-3293
Lucia VenneriDepartment of Cardiac MRI, Royal Free London NHS Foundation Trust, London, UK.
Tushar KotechaNational Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust, London, UK.ORCID 0000-0003-0059-4817
Ana Martinez-NaharroDepartment of Cardiac MRI, Royal Free London NHS Foundation Trust, London, UK.
Peter KellmanNational Heart, Lung, and Blood Institute, National Institute of Health, Bethesda, MD, USA.ORCID 0000-0002-9875-6070
Ann M Scott-RussellDepartment of Rheumatology, Queen Alexandra Hospital, Portsmouth, UK.
Benjamin E SchreiberNational Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust, London, UK.
Voon H OngCentre for Rheumatology and Connective Tissue Diseases, UCL Medical School (Royal Free Campus), London, UK.
Christopher P DentonCentre for Rheumatology and Connective Tissue Diseases, UCL Medical School (Royal Free Campus), London, UK.ORCID 0000-0003-3975-8938
Marianna FontanaDepartment of Cardiac MRI, Royal Free London NHS Foundation Trust, London, UK.ORCID 0000-0002-9233-9831
J Gerry CoghlanNational Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust, London, UK.
Vivek MuthuranguInstitute of Cardiovascular Science, University College London, London, UK.

Funding

Gadgetron Global Network and Intelligence Computing: Clinical Imaging Application Development and Software InfrastructureZIAHL006214 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI KELLMAN, PETER · 2016 to 2025
$7.3M
British Heart Foundation FS/CRLF/20/23004
6 · The paper itself

Abstract

objectivesMeasures of right heart size and function are prognostic in systemic sclerosis-associated pulmonary hypertension (SSc-PH), but the importance of myocardial tissue characterisation remains unclear. We aimed to investigate the predictive potential and interaction of cardiovascular magnetic resonance (CMR) myocardial tissue characterisation and right heart size and function in SSc-PH.

methodsA retrospective, single-centre, observational study of 148 SSc-PH patients confirmed by right heart catheterization who underwent clinically indicated CMR including native myocardial T1 and T2 mapping from 2016 to 2023 was performed.

resultsSixty-six (45%) patients died during follow-up (median 3.5 years, range 0.1-7.3). Patients who died were older (65 vs 60 years, P = 0.035) with more dilated (P < 0.001), hypertrophied (P = 0.013) and impaired (P < 0.001) right ventricles, more dilated right atria (P = 0.043) and higher native myocardial T1 (P < 0.001).After adjustment for age, indexed right ventricular end-systolic volume (RVESVi, P = 0.0023) and native T1 (P = 0.0024) were independent predictors of all-cause mortality. Both RVESVi and native T1 remained independently predictive after adjusting for age and PH subtype (RVESVi P < 0.001, T1 P = 0.0056). Optimal prognostic thresholds for RVESVi and native T1 were ≤38 mL/m2 and ≤1119 ms, respectively (P < 0.001). Patients with RVESVi ≤ 38 mL/m2 and native T1 ≤ 1119 ms had significantly better outcomes than all other combinations (P < 0.001). Furthermore, patients with RVESVi > 38mL/m2 and native T1 ≤ 1119 ms had significantly better survival than patients with RVESVi > 38mL/m2 and native T1 > 1119ms (P = 0.017).

conclusionWe identified prognostically relevant CMR metrics and thresholds for patients with SSc-PH. Assessing myocardial tissue characterisation alongside right ventricular function confers added value in SSc-PH and may represent an additional treatment target.

Indexed as

Heart VentriclesHypertension, PulmonaryScleroderma, SystemicAgedFemaleHumansMagnetic Resonance ImagingMagnetic Resonance Imaging, CineMaleMiddle AgedMyocardiumPredictive Value of TestsPrognosisRetrospective StudiesVentricular Function, RightCMRprognosispulmonary hypertensionright ventriclesystemic sclerosisT1 mapping

Identifiers

PMID38759116
PMCPMC11443025

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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.