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Título
Plasma exchange in anti-signal recognition particle myopathy: A systematic review and combined analysis of patient Individual data
Autor(es)
Palabras clave
Anti-SRP myopathy
Immune-mediated inflammatory myopathy
Plasma exchange
Plasmapheresis
Fecha de publicación
2024-04-27
Editor
MDPI
Citación
Martínez-Rodríguez, P., Escribano-Iglesias, M., Crisolino-Pozas, Á., Cubino-Boveda, N., López-Parra, M., Marcos, M., & Chamorro, A. (2024). Plasma Exchange in Anti-Signal Recognition Particle Myopathy: A Systematic Review and Combined Analysis of Patient Individual Data. Journal Of Personalized Medicine, 14(5), 461. https://doi.org/10.3390/jpm14050461
Resumen
[EN]Anti-signal recognition particle myopathy (anti-SRP myopathy) is a rare subtype of immune-mediated inflammatory myopathy characterized by muscle weakness and anti-SRP autoantibodies. Although plasma exchange (PE) is used in severe cases, its role remains unclear. A systematic review was conducted following PRISMA guidelines, identifying 23 patients with anti-SRP myopathy treated with PE. Data on demographics, clinical features, laboratory findings, treatments, and outcomes were analyzed combining individual patient data if available. Sixteen (69.6%) patients were male, with muscle weakness as the predominant symptom in 100% of cases. After PE, most patients showed improvement in symptoms, and the proportion of patients with muscle weakness was reduced (p = 0.001). Relapse occurred in 17.4% of the cases. The incidence of adverse events was low (8.7%). Despite limitations, including a small sample size and heterogeneous data, our systematic review suggests that PE may be effective in inducing remission and controlling symptoms in anti-SRP myopathy, particularly in severe cases. Since evidence on PE in anti-SRP myopathy is limited, further research, including prospective multicenter studies, is warranted to understand better its efficacy and safety and establish its role in treatment algorithms.
URI
ISSN
2075-4426
DOI
10.3390/jpm14050461
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