All participants underwent two CMR scans (visit 1, visit 2) at least 1 year apart. Patients’ follow‐up ended in August 2018. Clinical data were collected at both visits and included demographics, disease subtype and duration, organ involvement, and current and any change in DMARD and/or vasodilator treatment, including calcium channel blockers (CCBs), iloprost, sildenafil, bosentan, and angiotensin‐converting enzyme inhibitor (ACEI) between the two visits. Iloprost infusion was administered as a 3‐day schedule every 3 months at a dosing regimen of 100 μg, as per Leeds Teaching Hospital National Health Service trust protocol. Serum samples were collected for high‐sensitivity troponin I (hs‐TnI) and N‐terminal pro–brain natriuretic peptide (NT‐proBNP) testing at both visits. hs‐TnI was measured on a Siemens Advia XPT system (Advia Chemistry XPT and Advia Centaur XPT Immunoassay) and NT‐proBNP was measured on Cobas 6000 (immunochemistry module Cobas e601) at both visits. Patients had annual pulmonary function tests (PFTs) performed as part of routine clinical assessment. The PFT measures approximating to each CMR visit were recorded.