» Articles » PMID: 33360322

Myositis-specific and Myositis-associated Autoantibodies in a Large Indian Cohort of Inflammatory Myositis

Overview
Specialty Rheumatology
Date 2020 Dec 28
PMID 33360322
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The Idiopathic Inflammatory Myositis (IIM) are heterogenous with distinct clinical phenotypes associated with specific myositis specific antibodies (MSA) and myositis associated antibodies (MAA).

Objectives: To evaluate the frequency, pattern and associations of MSA/MAA in a large Indian cohort of IIM.

Methods: Adult and juvenile IIM (2017 ACR/EULAR criteria), were recruited in the MyoCite cohort between 2017and 2020 at a tertiary center in Northern India. Standardized clinical and laboratory variables were extracted from the database archive. Serum samples were evaluated for the presence of MSAs/MAAs by Line immunoassay and anti-nuclear antibodies (ANA) by Immunofluorescence assay (IFA). The prevalence and clinical associations of different MSA/MAAs were assessed.

Results: MSA and MAAs were tested in 250 IIM patients (214 adults, 36 children) of age [40 (3049), 13 (7.5-16) years] and disease duration [ 7 (3-17), 6 (2-17) months] comprising predominantly of Dermatomyositis (DM) followed by Overlap myositis (OM). MSAs/MAAs were found in 148 (59.2%, 60.7% adults and 50% JIIM), of which two-thirds were MSA (95, 64% overall). Two cases (0.8%) had more than one MSA. In adult IIM, the most common MSA was anti-Jo-1 (10%), whereas it was anti-MDA5 and anti-NXP2 4 (11%) each in Juvenile IIM (JIIM). 76.0% (172/226) were ANA positive, with speckled pattern being the most common (37%,). Nearly two-thirds (54, 61%) of those with negative ANA had MSA/ MAA. Nearly half (18/54, 54.6%) had MSA associated with cytoplasmic patterns. ARS (anti-aminoacyl-tRNA synthetase) were associated with mechanic's hands (OR-7.06), ILD (OR-4.4), and arthritis (OR-2.23). Clinical associations of anti-Jo-1 and non-Jo-1 Anti synthetase syndrome (ASS) did not differ. Anti-MDA-5 associated with oral ulcers (OR-8.3), fever (OR-8.6) and weight loss (OR-7.35) in adults, and arthritis (OR-11.5), and periungual rash (OR-9.6) in children. Anti-TIF-1γ associated with photosensitivity (OR-10.44) and malignancy (OR-34) in adults, and cuticular overgrowth (OR-11.2) in children.

Conclusion: Myositis autoantibodies are seen in two-thirds IIMs and are associated with distinct clinical subsets. Jo-1 and non-Jo-1 ASS exhibit similar characteristics. The association of anti-TIF1 γ with malignancy was confirmed in adults. MSA/MAA were present in two-thirds of those with negative ANA and MSA were nearly always mutually exclusive.

Citing Articles

Clinical characteristics and prognosis of amyopathic dermatomyositis patients with interstitial lung disease: insights from a retrospective cohort.

Ying Y, Wu T, Wang L, Zhang Y, Yu Y, Deng Z Orphanet J Rare Dis. 2025; 20(1):53.

PMID: 39915831 PMC: 11804100. DOI: 10.1186/s13023-025-03575-w.


An update on autoantibodies in the idiopathic inflammatory myopathies.

Allameen N, Ramos-Lisbona A, Wedderburn L, Lundberg I, Isenberg D Nat Rev Rheumatol. 2024; 21(1):46-62.

PMID: 39609638 DOI: 10.1038/s41584-024-01188-4.


Immunohistochemical expression in idiopathic inflammatory myopathies at a single center in Vietnam.

Ngo D, Le S, Phan K, Doan T, Nguyen L, Dang M J Pathol Transl Med. 2024; 58(4):174-181.

PMID: 38910358 PMC: 11261171. DOI: 10.4132/jptm.2024.05.02.


Idiopathic Inflammatory Myopathies.

Balan S, Madan S Indian J Pediatr. 2023; 91(10):1041-1048.

PMID: 37919486 DOI: 10.1007/s12098-023-04896-z.


Clinical profile of anti-NXP-2 antibody-positive inflammatory myositis and outcome in an Indian population.

Manwatkar A, Padiyar S, Nair A, Jha A, Kumar S, Yadav B Clin Rheumatol. 2023; 42(12):3289-3297.

PMID: 37801141 DOI: 10.1007/s10067-023-06751-0.