Cardiac Sarcoidosis: When and How to Treat Inflammation

Author:

Giblin Gerard T1ORCID,Murphy Laura2ORCID,Stewart Garrick C1ORCID,Desai Akshay S1ORCID,Di Carli Marcelo F2ORCID,Blankstein Ron2ORCID,Givertz Michael M1ORCID,Tedrow Usha B3ORCID,Sauer William H3ORCID,Hunninghake Gary M4ORCID,Dellaripa Paul F4ORCID,Divakaran Sanjay1ORCID,Lakdawala Neal K1ORCID

Affiliation:

1. Center for Advanced Heart Disease, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, US

2. Cardiovascular Imaging Program and Departments of Medicine and Radiology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, US

3. Cardiac Arrhythmia Service, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, US

4. Interstitial Lung Disease Program, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, US

Abstract

Sarcoidosis is a complex, multisystem inflammatory disease with a heterogeneous clinical spectrum. Approximately 25% of patients with systemic sarcoidosis will have cardiac involvement that portends a poorer outcome. The diagnosis, particularly of isolated cardiac sarcoidosis, can be challenging. A paucity of randomised data exist on who, when and how to treat myocardial inflammation in cardiac sarcoidosis. Despite this, corticosteroids continue to be the mainstay of therapy for the inflammatory phase, with an evolving role for steroid-sparing and biological agents. This review explores the immunopathogenesis of inflammation in sarcoidosis, current evidence-based treatment indications and commonly used immunosuppression agents. It explores a multidisciplinary treatment and monitoring approach to myocardial inflammation and outlines current gaps in our understanding of this condition, emerging research and future directions in this field.

Funder

Harvard Catalyst

Publisher

Radcliffe Group Ltd

Subject

General Medicine

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