A multidisciplinary approach to the diagnosis of antisynthetase syndrome

Matthew Wells, Sughra Alawi, Kyaing Yi Mon Thin, Harsha Gunawardena, Adrian R Brown, Anthony Edey, John D Pauling, Shaney L Barratt, Huzaifa I Adamali*

*Corresponding author for this work

Research output: Contribution to journalReview article (Academic Journal)peer-review

12 Citations (Scopus)
227 Downloads (Pure)

Abstract

Antisynthetase syndrome is a subtype of idiopathic inflammatory myopathy, strongly associated with the presence of interstitial lung disease. Diagnosis is made by identifying myositis-specific antibodies directed against aminoacyl tRNA synthetase, and relevant clinical and radiologic features. Given the multisystem nature of the disease, diagnosis requires the careful synthesis of subtle clinical and radiological features with the interpretation of specialized autoimmune serological testing. This is provided in a multidisciplinary environment with input from rheumatologists, respiratory physicians, and radiologists. Differentiation from other idiopathic interstitial lung diseases is key; treatment and prognosis differ between patients with antisynthetase syndrome and idiopathic interstitial lung disease. In this review article, we look at the role of the multidisciplinary team and its individual members in the initial diagnosis of the antisynthetase syndrome, including the role of physicians, radiologists, and the wider team.
Original languageEnglish
Article number959653
Number of pages14
JournalFrontiers in Medicine
Volume9
DOIs
Publication statusPublished - 14 Sept 2022

Bibliographical note

Funding Information:
Funding for the publication of this article has been kindly provided by the Bristol Interstitial Lung Disease Research Fund.

Funding Information:
The authors thank Sarah Rudd, librarian, North Bristol NHS Trust and also Dr Chan and Dr Andrade of ANApatterns.org.

Publisher Copyright:
Copyright © 2022 Wells, Alawi, Thin, Gunawardena, Brown, Edey, Pauling, Barratt and Adamali.

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