Skeletal Muscle Involvement in Antisynthetase Syndrome.

Abstract

Importance:

Antisynthetase syndrome, characterized by myositis, interstitial lung disease, skin rash, arthropathy, and Raynaud phenomenon, is a clinical entity based on the presence of aminoacyl transfer RNA synthetase (ARS) antibodies in patients' serum. However, antisynthetase syndrome is not included in the histological subsets of idiopathic inflammatory myopathies.

Objective:

To elucidate the clinical features of myositis in patients with antisynthetase syndrome.

Design, Setting, and Participants:

In this cohort study, muscle biopsy and blood samples were collected from 460 patients with idiopathic inflammatory myositis from various regional referral centers throughout Japan between October 2010 and December 2014. Data were analyzed in March 2016.

Exposures:

Six different anti-ARS antibodies were detected in serum by RNA immunoprecipitation. Line blot assay and protein immunoprecipitation were also performed. HLA-DRB1 alleles were genotyped.

Main Outcomes and Measures:

The main outcomes were muscle manifestations and histological findings. Predisposing factors, extramuscular symptoms, and follow-up information were also studied.

Results:

Of 460 patients with idiopathic inflammatory myopathies, 51 (11.1%) had anti-ARS antibodies. Of this subset, 31 (61%) were women, with a mean (SD) age at disease onset of 60.2 (16.1) years. Among 6 different anti-ARS antibodies, only 1-the anti-OJ antibody-was not detected by line blot assay but by RNA immunoprecipitation. There were no significant HLA-DRB1 alleles associated with anti-ARS antibodies. All 51 patients presented with muscle limb weakness; 14 (27%) had severe limb weakness, 17 (33%) had neck muscle weakness, 15 (29%) had dysphagia, and 15 (29%) had muscle atrophy. Although patients with anti-OJ antibodies showed severe muscle weakness, the clinical presentations of antisynthetase syndrome were relatively homogeneous. In histology, perifascicular necrosis, the characteristic finding of antisynthetase syndrome, was found in 24 patients (47%). Myositis with anti-ARS antibodies responded to the combination of immunosuppressive therapy with favorable outcomes. Interstitial lung disease, found in 41 patients (80%), was more closely associated with mortality than myositis.

Conclusions and Relevance:

Although clinical presentations of antisynthetase syndrome were relatively homogeneous, anti-OJ antibodies were associated with severe muscle involvement. Antisynthetase syndrome is a clinical and histological subset among idiopathic inflammatory myopathies.

• Authors: Eri Noguchi, Akinori Uruha, Shigeaki Suzuki, Kohei Hamanaka, Yuko Ohnuki, Jun Tsugawa, Yurika Watanabe, Jin Nakahara, Takashi Shiina, Norihiro Suzuki, Ichizo Nishino
• Journal: JAMA neurology (JAMA Neurol) Vol. 74 Issue 8 Pg. 992-999 (08 01 2017) ISSN: 2168-6157 [Electronic] United States
• PMID: 28586844 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Autoantibodies
• HLA-DRB1 Chains
• Amino Acyl-tRNA Synthetases

Topics

• Adolescent
• Adult
• Aged
• Aged, 80 and over
• Amino Acyl-tRNA Synthetases (immunology)
• Autoantibodies (blood)
• Cohort Studies
• Electromyography
• Female
• Genotype
• HLA-DRB1 Chains (genetics)
• Humans
• Immunoprecipitation
• Magnetic Resonance Imaging
• Male
• Middle Aged
• Muscle, Skeletal (diagnostic imaging, metabolism, physiopathology)
• Myositis (complications, genetics, immunology, pathology)
• Statistics, Nonparametric
• Young Adult