Evidence map›Paper›PMID 40130472›Full record

ArticleEuropean journal of neurology2025

Testing for Acetylcholine Receptor and Muscle-Specific Tyrosine Kinase Antibodies by Fixed Cell-Based Assay in Clinical Practice: Positive Predictive Value for Myasthenia Gravis.

Cathy Meng Fei Li, Michael W Nicolle, Kamala Sangam, Liju Yang, Adrian Budhram

Abstract read
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Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Cathy Meng Fei LiDepartment of Clinical Neurological Sciences, Western University, London Health Sciences Centre, London, Ontario, Canada.
Michael W NicolleDepartment of Clinical Neurological Sciences, Western University, London Health Sciences Centre, London, Ontario, Canada.
Kamala SangamDepartment of Clinical Neurological Sciences, Western University, London Health Sciences Centre, London, Ontario, Canada.
Liju YangDepartment of Pathology and Laboratory Medicine, Western University, London Health Sciences Centre, London, Ontario, Canada.
Adrian BudhramDepartment of Clinical Neurological Sciences, Western University, London Health Sciences Centre, London, Ontario, Canada.ORCID 0000-0003-4860-0470

Funding

American Academy of Neurology
6 · The paper itself

Abstract

backgroundFixed cell-based assays (CBAs) to detect acetylcholine receptor and muscle-specific tyrosine kinase antibodies (anti-AChR/MuSK) are now available, but evaluations of their diagnostic performance in clinical practice are lacking. We examined the positive predictive value (PPV) of anti-AChR/MuSK fixed CBA for myasthenia gravis (MG), following the implementation of this assay as first-line testing at our centre.

methodsWe identified all patients at our centre with positive anti-AChR/MuSK fixed CBA results between November 2021 and July 2024. Clinical information was reviewed to classify patients as having true positive or false positive antibody results. Patients with a clinical presentation compatible with MG and no more likely alternative diagnosis were classified as true positives, whereas all others were classified as false positives. Test PPV was calculated as the proportion of positives that were classified as true positives.

resultsOf 770 patients who underwent anti-AChR/MuSK fixed CBA testing, 109 (14%) had positive antibody results (Anti-AChR, 105; Anti-MuSK, 4). Among them, one patient with anti-AChR positivity was classified as a false positive (suspected thymic hyperplasia without neurologic symptoms). The remaining 108 patients were classified as true positives, resulting in a calculated PPV of 99%.

conclusionsWe found that anti-AChR/MuSK fixed CBA had excellent PPV for MG. Anti-AChR positivity in one asymptomatic patient with suspected thymic hyperplasia was classified as a false positive result, although the possibility that it represents a true marker of thymic pathology in a patient who may later develop MG is challenging to exclude. The high PPV reported herein supports the use of anti-AChR/MuSK fixed CBA as first-line testing for suspected MG.

Indexed as

AutoantibodiesMyasthenia GravisReceptor Protein-Tyrosine KinasesReceptors, CholinergicAdultAgedFemaleHumansMaleMiddle AgedPredictive Value of TestsYoung AdultAutoantibodiesMUSK protein, humanReceptor Protein-Tyrosine KinasesReceptors, Cholinergicacetylcholine receptor antibodycell‐based assaymuscle‐specific tyrosine kinase antibodymyasthenia gravispositive predictive value

Identifiers

PMID40130472
PMCPMC11933831

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