Medicine

DeAnna Baker Frost, R. Tedford, Richard M. Silver

2026.3.1BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY

DOI: 10.1016/j.berh.2026.102134

Abstract

Systemic sclerosis (SSc) is an autoimmune disease characterized by chronic inflammation leading to fibrosis in the skin and organs, including the heart. It is classified as SSc-primary heart involvement (pHI), defined as heart dysfunction primarily caused by SSc, excluding other causes. Several disease manifestations, including conduction abnormalities, cardiac arrythmias, myocarditis/pericardial involvement, heart failure (systolic and diastolic) and valvular dysfunction, are categorized within SSc-pHI. SSc-pHI has a high prevalence, high mortality, and increased risk for sudden cardiac death. Serum biomarkers, high sensitivity troponin and NT-proBNP, may help in screening, with electrocardiography, echocardiography, and Holter monitoring. Cardiac magnetic resonance imaging (cMRI) can confirm SSc-pHI and is considered gold standard for diagnosis, with limited use due to cost and availability. Treatment approaches are multifaceted depending on the manifestation of SSc-pHI but often require immunosuppression at a minimum. A multidisciplinary team including rheumatologists and cardiologists offers the best approach for diagnosis, management, and monitoring.

Citation format

FROST, DeAnna Baker; TEDFORD, R.; SILVER, Richard M. Definition, diagnosis, treatment for scleroderma primary heart involvement. BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2026: 102134.