Distinct cardiovascular phenotypes are associated with prognosis in systemic sclerosis: a cardiovascular magnetic resonance study

Author:

Knight Daniel S1234ORCID,Karia Nina124ORCID,Cole Alice R5,Maclean Rory H5,Brown James T124,Masi Ambra23,Patel Rishi K26ORCID,Razvi Yousuf26ORCID,Chacko Liza26,Venneri Lucia2,Kotecha Tushar1234ORCID,Martinez-Naharro Ana236,Kellman Peter7ORCID,Scott-Russell Ann M8,Schreiber Benjamin E1,Ong Voon H5,Denton Christopher P5ORCID,Fontana Marianna26ORCID,Coghlan J Gerry13,Muthurangu Vivek4

Affiliation:

1. National Pulmonary Hypertension Service, Royal Free London NHS Foundation Trust , Pond Street, London, NW3 2QG , UK

2. UCL Department of Cardiac MRI, University College London (Royal Free Campus) , Rowland Hill Street, London, NW3 2PF , UK

3. Department of Cardiology, Royal Free London NHS Foundation Trust , Pond Street, London, NW3 2QG , UK

4. UCL Institute of Cardiovascular Science, University College London , Gower Street, London, WC1E 6BT , UK

5. Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School (Royal Free Campus), Rowland Hill Street , London, NW3 2PF , UK

6. National Amyloidosis Centre, Division of Medicine, University College London , Rowland Hill Street, London, NW3 2PF , UK

7. National Heart, Lung, and Blood Institute, National Institute of Health , 31 Center Dr, Bethesda, MD 20892 , USA

8. Department of Rheumatology, Queen Alexandra Hospital , Cosham, Portsmouth, PO6 3LY , UK

Abstract

Abstract Aims Cardiovascular involvement in systemic sclerosis (SSc) is heterogeneous and ill-defined. This study aimed to: (i) discover cardiac phenotypes in SSc by cardiovascular magnetic resonance (CMR); (ii) provide a CMR-based algorithm for phenotypic classification; and (iii) examine for associations between phenotypes and mortality. Methods and results A retrospective, single-centre, observational study of 260 SSc patients who underwent clinically indicated CMR including native myocardial T1 and T2 mapping from 2016 to 2019 was performed. Agglomerative hierarchical clustering using only CMR variables revealed five clusters of SSc patients with shared CMR characteristics: dilated right hearts with right ventricular failure (RVF); biventricular failure dilatation and dysfunction (BVF); and normal function with average cavity (NF-AC), normal function with small cavity (NF-SC), and normal function with large cavity (NF-LC) sizes. Phenotypes did not co-segregate with clinical or antibody classifications. A CMR-based decision tree for phenotype classification was created. Sixty-three (24%) patients died during a median follow-up period of 3.4 years. After adjustment for age and presence of pulmonary hypertension (PH), independent CMR predictors of all-cause mortality were native T1 (P < 0.001) and right ventricular ejection fraction (RVEF) (P = 0.0032). NF-SC and NF-AC groups had more favourable prognoses (P≤0.036) than the other three groups which had no differences in prognoses between them (P > 0.14). Hazard ratios (HR) were statistically significant for RVF (HR = 8.9, P < 0.001), BVF (HR = 5.2, P = 0.006), and NF-LC (HR = 4.9, P = 0.002) groups. The NF-LC group remained significantly predictive of mortality after adjusting for RVEF, native T1, and PH diagnosis (P = 0.0046). Conclusion We identified five CMR-defined cardiac SSc phenotypes that did not co-segregate with clinical data and had distinct outcomes, offering opportunities for a more precision-medicine based management approach.

Funder

British Heart Foundation

Clinical Research Leave Fellowship

National Institute for Health Research

University College London Hospitals

Biomedical Research Centre

BHF Intermediate Fellowship

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine

Reference32 articles.

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3. Subclinical myocardial inflammation and diffuse fibrosis are common in systemic sclerosis–a clinical study using myocardial T1-mapping and extracellular volume quantification;Ntusi;J Cardiovasc Magn Reson,2014

4. T1 mapping cardiac magnetic resonance imaging frequently detects subclinical diffuse myocardial fibrosis in systemic sclerosis patients;Poindron;Semin Arthritis Rheum,2020

5. Quantification of myocardial extracellular volume fraction with cardiac MR imaging for early detection of left ventricle involvement in systemic sclerosis;Thuny;Radiology,2014

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