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

Author:

Knight Daniel S123ORCID,Virsinskaite Ruta123,Karia Nina13,Cole Alice R4,Maclean Rory H4,Brown James T123,Patel Rishi K25ORCID,Razvi Yousuf25ORCID,Venneri Lucia2,Kotecha Tushar123ORCID,Martinez-Naharro Ana2,Kellman Peter6ORCID,Scott-Russell Ann M7,Schreiber Benjamin E1,Ong Voon H4,Denton Christopher P4ORCID,Fontana Marianna25ORCID,Coghlan J Gerry1,Muthurangu Vivek3

Affiliation:

1. National Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust , London, UK

2. Department of Cardiac MRI, Royal Free London NHS Foundation Trust , London, UK

3. Institute of Cardiovascular Science, University College London , London, UK

4. Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School (Royal Free Campus) , London, UK

5. Division of Medicine, University College London , London, UK

6. National Heart, Lung, and Blood Institute, National Institute of Health , Bethesda, MD, USA

7. Department of Rheumatology, Queen Alexandra Hospital , Portsmouth, UK

Abstract

Abstract Objectives Measures 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. Methods A 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. Results Sixty-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). Conclusion We 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.

Funder

British Heart Foundation

Publisher

Oxford University Press (OUP)

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