Clinical Presentation and Treatment of High-Risk Sarcoidosis

Research output: Contribution to journalReview articlepeer-review

4 Scopus citations

Abstract

Sarcoidosis is a multisystem disease of unknown cause with heterogeneous clinical manifestations and variable course. Spontaneous remissions occur in some patients, whereas others have progressive disease impacting survival, organ function, and quality of life. Four high-risk sarcoidosis phenotypes associated with chronic inflammation have recently been identified as highpriority areas for research. These include treatment-refractory pulmonary disease, cardiac sarcoidosis, neurosarcoidosis, and multiorgan sarcoidosis. Significant gaps currently exist in the understanding of these high-risk manifestations of sarcoidosis, including their natural history, diagnostic criteria, biomarkers, and the treatment strategy, such as the ideal agent, optimal dose, and treatment duration. The use of registries with wellphenotyped patients is a critical first step to study high-risk sarcoidosis manifestations systematically. We review the diagnostic and treatment approach to high-risk sarcoidosis manifestations. Appropriately identifying these disease subgroups will help enroll well-phenotyped patients in sarcoidosis registries and clinical trials, a necessary step to narrow existing gaps in understanding of this enigmatic disease.

Original languageEnglish (US)
Pages (from-to)1935-1947
Number of pages13
JournalAnnals of the American Thoracic Society
Volume18
Issue number12
Early online dateSep 15 2021
DOIs
StatePublished - Dec 2021

Bibliographical note

Publisher Copyright:
© 2021 by the American Thoracic Society.

Keywords

  • Cardiac sarcoidosis
  • High-risk sarcoidosis
  • Multiorgan sarcoidosis
  • Neurosarcoidosis
  • Progressive pulmonary sarcoidosis

PubMed: MeSH publication types

  • Journal Article
  • Review

Fingerprint

Dive into the research topics of 'Clinical Presentation and Treatment of High-Risk Sarcoidosis'. Together they form a unique fingerprint.

Cite this