A North American Cohort of Anti-SAE Dermatomyositis: Clinical Phenotype, Testing, and Review of Cases.
Journal
ACR open rheumatology
ISSN: 2578-5745
Titre abrégé: ACR Open Rheumatol
Pays: United States
ID NLM: 101740025
Informations de publication
Date de publication:
May 2021
May 2021
Historique:
received:
25
11
2020
accepted:
19
02
2021
pubmed:
29
3
2021
medline:
29
3
2021
entrez:
28
3
2021
Statut:
ppublish
Résumé
Antibodies against the small ubiquitin-like modifier (SUMO) activating enzyme (SAE) are one of the rarer specificities associated with dermatomyositis (DM). The purpose of this study is to describe the clinical characteristics of patients with anti-SAE autoantibodies in a North American cohort and to ascertain cancer prevalence. We also describe the performance characteristics of the line blotting (Euroimmun) method for antibody detection compared with an immunoprecipitation-based assay. Sera from 2127 patients suspected of having myositis were assayed for myositis-specific autoantibodies using the Euroimmun platform. Those positive for SAE autoantibodies were assayed by a second method (immunoprecipitation) for confirmation. Only those cases positive by both methods were taken as definite cases of anti-SAE-positive DM. Chart reviews of these patients were completed to obtain information on clinical characteristics, cancer history, and treatment. Forty-three of 2127 sera were anti-SAE autoantibody positive by Euroimmun (≥15 units, +); of these, only 19 were confirmed positive by immunoprecipitation. All 19 cases had skin involvement and varying presentations of muscle, lung, and joint disease. Cancer occurred coincident with DM in two patients, and cancers were detected more than 5 years from symptom onset in three patients. In a population of suspected inflammatory myositis, a higher cutoff on line blot testing (≥36 units, ++) yielded better agreement with immunoprecipitation methods. SAE autoantibodies associate with a clinical phenotype of DM, which most commonly presents with a rash first, followed by muscle involvement and varying extramuscular involvement. As coincident cancer was seen in anti-SAE-positive DM, judicious malignancy screening may be warranted.
Identifiants
pubmed: 33774928
doi: 10.1002/acr2.11247
pmc: PMC8126760
doi:
Types de publication
Journal Article
Langues
eng
Pagination
287-294Subventions
Organisme : NIAMS NIH HHS
ID : K23AR075898
Pays : United States
Organisme : Jerome L. Greene Foundation
Organisme : NIAMS NIH HHS
ID : P30-AR070254
Pays : United States
Organisme : NIAMS NIH HHS
ID : K23 AR075898
Pays : United States
Organisme : Huayi and Siuling Zhang Discovery Fund
Organisme : NIAMS NIH HHS
ID : K23 AR073927
Pays : United States
Organisme : Cupid Foundation
Organisme : Donald B. and Dorothy L. Stabler Foundation
Organisme : NIAMS NIH HHS
ID : P30 AR070254
Pays : United States
Informations de copyright
© 2021 The Authors. ACR Open Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.
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