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Concordance between radioimmunoassay and fixed cell‐based assay in subjects without myasthenia gravis: optimizing the diagnostic approach.

Authors :
Falso, Silvia
Marini, Sofia
Carrozza, Cinzia
Sabatelli, Eleonora
Mascagna, Giovanni
Marini, Martina
Morroni, Jacopo
Evoli, Amelia
Iorio, Raffaele
Source :
European Journal of Neurology. Aug2024, p1. 5p. 1 Illustration.
Publication Year :
2024

Abstract

Background and Purpose Methods Results Conclusions Acetylcholine receptor antibody (AChR‐Ab) detection is crucial in myasthenia gravis (MG) diagnosis and, currently, the radioimmunoassay (RIA) is the gold standard. However, RIA may detect AChR‐Ab against nonpathogenic intracellular epitopes. In this study, we performed fixed cell‐based assay (F‐CBA) in RIA‐AChR‐Ab positive subjects without MG symptoms, to assess whether F‐CBA could show a higher specificity compared to RIA in detecting pathogenic Abs.We reviewed medical records of patients referred to our MG outpatient clinic because of RIA‐AChR‐Ab detection. MG diagnosis was based on clinical examination, electrophysiology and Ab detection. AChR‐Abs were tested by RIA in the whole cohort. Serum samples from RIA‐positive asymptomatic subjects were retested by F‐CBA.Of 605 subjects who tested RIA‐AChR‐Ab positive, MG diagnosis was confirmed in 599. Six subjects were RIA‐AChR‐Ab positive although they had never had MG symptoms; in four of these subjects AChR‐Abs were not detected by F‐CBA, whereas the remaining two (both non‐MG thymoma cases) were positive also by F‐CBA.RIA false positivity for AChR‐Ab is very rare. Previous literature has demonstrated that F‐CBA has higher sensitivity than RIA for MG, especially in ocular cases. Our preliminary results show that, in rare instances, F‐CBA may be more specific than RIA for MG diagnosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13515101
Database :
Academic Search Index
Journal :
European Journal of Neurology
Publication Type :
Academic Journal
Accession number :
178900063
Full Text :
https://doi.org/10.1111/ene.16435