Myocarditis in anti-synthetase syndrome: clinical features and diagnostic modalities

Author:

De Luca Giacomo12ORCID,Campochiaro Corrado12ORCID,Palmisano Anna23ORCID,Bruno Elisa23,Vignale Davide23ORCID,Peretto Giovanni4,Sala Simone4ORCID,Ferlito Arianna12,Cilona Maria Bernardette12,Esposito Antonio23,Matucci-Cerinic Marco15,Dagna Lorenzo12

Affiliation:

1. Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Hospital , Milan, Italy

2. School of Medicine, Vita-Salute San Raffaele University , Milan, Italy

3. Clinical and Experimental Radiology Unit, Experimental Imaging Center, IRCCS San Raffaele Hospital , Milan, Italy

4. Department of Cardiac Electrophysiology and Arrhythmology, IRCCS San Raffaele Hospital and University , Milan, Italy

5. Department of Experimental and Clinical Medicine, University of Florence, and Division of Rheumatology AOUC , Florence, Italy

Abstract

Abstract Objectives Myocarditis is an overlooked manifestation of anti-synthetase syndrome (ASS). Our study describes the clinical and instrumental features of ASS myocarditis and evaluates the performance of cardiac MRI (CMRI) with mapping techniques in assisting diagnosis of ASS myocarditis. Methods Data from patients with ASS were retrospectively analysed. CMRI data for patients diagnosed with myocarditis, including late gadolinium enhancement (LGE), T2 ratio, T1 mapping, extracellular volume (ECV) and T2 mapping, were reviewed. Myocarditis was defined by the presence of symptoms and/or signs suggestive for heart involvement, including increased high-sensitive troponin T (hs-TnT) and/or N-terminal pro-brain natriuretic peptide (NT-proBNP), and at least an instrumental abnormality. The clinical features of patients with ASS with and without myocarditis were compared. A P-value of <0.05 was considered statistically significant. Results Among a cohort of 43 patients with ASS [median age 58 (48.0–66.0) years; females 74.4%; anti-Jo1 53.5%], 13 (30%) were diagnosed with myocarditis. In 54% of those 13 patients, myocarditis was diagnosed at clinical onset. All patients with ASS with myocarditis had at least one CMRI abnormality: increased ECV in all cases, presence of LGE in 91%, and increased T1 and T2 mapping in 91%. The 2009 Lake Louise criteria (LLC) were satisfied by 6 patients, and the 2018 LLC by 10 patients. With the updated LLC, the sensitivity for myocarditis improved from 54.6% to 91.0%. Patients with ASS with myocarditis were more frequently males (53% vs 13%; P = 0.009) with fever (69% vs 17%; P = 0.001), and had higher hs-TnT [88.0 (23.55–311.5) vs 9.80 (5.0–23.0) ng/l; P < 0.001], NT-proBNP [525.5 (243.5–1575.25) vs 59.0 (32.0–165.5; P = 0.013) pg/ml; P = 0.013] and CRP [7.0 (1.7–15.75) vs 1.85 (0.5–2.86) mg/l; P = 0.011] compared with those without myocarditis. Conclusion In ASS, myocarditis is frequent, even at clinical onset. Patients with ASS with myocarditis frequently presented with fever and increased CRP, suggesting the existence of an inflammatory phenotype. The use of novel CMRI mapping techniques may increase diagnostic sensitivity for myocarditis in ASS.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Reference35 articles.

1. The diagnosis and treatment of antisynthetase syndrome;Witt;Clin Pulm Med,2016

2. Myocarditis in patients with antisynthetase syndrome: prevalence, presentation, and outcomes;Dieval;Medicine (United States),2015

3. Fatal cardiac involvement complicating antisynthetase syndrome;Brady;BMJ Case Rep,2014

4. Brief report: antisynthetase syndrome-associated myocarditis;Sharma;J Card Fail,2014

5. Impact of systemic immune-mediated diseases on clinical features and prognosis of patients with biopsy-proved myocarditis;Peretto;Int J Cardiol,2019

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