No General Association Between Myositis Antibodies and Electromyography Findings

ABSTRACT Objective Myositis‐specific antibodies (MSAs), myositis‐associated antibodies (MAAs), and concentric needle electromyography (EMG) are routinely used in the differential diagnosis of myositis. Their mutual relationship, particularly between MSAs/MAAs and EMG findings, remains unclear. Methods We retrospectively analyzed the charts of 368 patients suspected of having myositis at a tertiary neurological center over a span of 7 years. They underwent EMG (fibrillations (Fibs), positive sharp waves (PSWs), fasciculations (Fascs), or complex repetitive discharges (CRD), motor unit action potential (MUAP) morphology, maximum MUAP amplitude, interference pattern, assessment of pathological EMG, and myopathic EMG) and MSA/MAA testing (Line Blot: anti−Mi2, −Ku, −PM‐Scl100, −PM‐Scl75, −Jo1, −SRP, −PL7, −PL12, −EJ, −OJ, −Ro52), and were categorized into myositis and non‐myositis diseases. Associations between pathological EMG findings and positive MSA/MAA were then tested. Results No general association was observed between positive MSAs/MAAs and pathological EMG findings; only a slightly significant association between positive MSAs/MAAs and the presence of a myopathic EMG assessment ( p = 0.043, φ = 0.113). Among 63 patients with myositis, 36 (57.1%) had positive MSA/MAA, 35 (55.6%) showed fibrillations/positive sharp waves, 17 (27.0%) had both, and 9 (14.3%) had neither. Discussion The presence of MSA/MAA does not necessarily indicate pathological EMG findings, and vice versa. Both may provide valuable insights into different aspects of myositis, acting as complementary elements in the diagnostic process.

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Journal
Neurology and Clinical Neuroscience
Published
2026-02-09
DOI
https://doi.org/10.1002/ncn3.70086
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
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article

No General Association Between Myositis Antibodies and Electromyography Findings

Marcel Armbruster, David L. Hoffmann, Evelyn Dubois, Justus Carl Marquetand et al.
Neurology and Clinical Neuroscience
Inflammatory Myopathies and Dermatomyositis
article

No General Association Between Myositis Antibodies and Electromyography Findings

Marcel Armbruster, David L. Hoffmann, Evelyn Dubois, Justus Carl Marquetand, Benedict Kleiser, Markus C. Kowarik, Alexander Grimm, Hanna Seifermann
article en

Abstract

ABSTRACT Objective Myositis‐specific antibodies (MSAs), myositis‐associated antibodies (MAAs), and concentric needle electromyography (EMG) are routinely used in the differential diagnosis of myositis. Their mutual relationship, particularly between MSAs/MAAs and EMG findings, remains unclear. Methods We retrospectively analyzed the charts of 368 patients suspected of having myositis at a tertiary neurological center over a span of 7 years. They underwent EMG (fibrillations (Fibs), positive sharp waves (PSWs), fasciculations (Fascs), or complex repetitive discharges (CRD), motor unit action potential (MUAP) morphology, maximum MUAP amplitude, interference pattern, assessment of pathological EMG, and myopathic EMG) and MSA/MAA testing (Line Blot: anti−Mi2, −Ku, −PM‐Scl100, −PM‐Scl75, −Jo1, −SRP, −PL7, −PL12, −EJ, −OJ, −Ro52), and were categorized into myositis and non‐myositis diseases. Associations between pathological EMG findings and positive MSA/MAA were then tested. Results No general association was observed between positive MSAs/MAAs and pathological EMG findings; only a slightly significant association between positive MSAs/MAAs and the presence of a myopathic EMG assessment ( p = 0.043, φ = 0.113). Among 63 patients with myositis, 36 (57.1%) had positive MSA/MAA, 35 (55.6%) showed fibrillations/positive sharp waves, 17 (27.0%) had both, and 9 (14.3%) had neither. Discussion The presence of MSA/MAA does not necessarily indicate pathological EMG findings, and vice versa. Both may provide valuable insights into different aspects of myositis, acting as complementary elements in the diagnostic process.

Neurology and Clinical NeuroscienceVol. 14(2)
Bernstein Center for Computational Neuroscience Tübingen (DE), Hertie Institute for Clinical Brain Research (DE), University of Tübingen (DE)
Openalex Percentile: Top 61%
Inflammatory Myopathies and Dermatomyositis
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