2026-04-14T09:24:58Zhttps://recercat.cat/oai/request
oai:recercat.cat:2445/1228692025-11-21T05:34:19Zcom_2072_1057col_2072_478917col_2072_478921
RECERCAT author Suárez Calvet, Xavier author Gallardo, Eduard author Pinal Fernandez, Iago author Luna, Noemí de author Lleixà, Cinta author Díaz Manera, Jordi author Rojas-Garcia, Ricard author Castellví, Ivan author Martínez, M. Angeles author Grau Junyent, Josep M. (Josep Maria) author Selva O'Callaghan, Albert author Illa Sendra, Isabel 2018-06-08T14:18:34Z2018-06-08T14:18:34Z2017-07-242018-06-08T14:18:35Z Background: Dermatomyositis (DM) is inflammatory myopathy or myositis characterized by muscle weakness and skin manifestations. In the differential diagnosis of DM the evaluation of the muscle biopsy is of importance among other parameters. Perifascicular atrophy in the muscle biopsy is considered a hallmark of DM. However, perifascicular atrophy is not observed in all patients with DM and, conversely, perifascicular atrophy can be observed in other myositis such as antisynthetase syndrome (ASS), complicating DM diagnosis. Retinoic acid inducible-gene I (RIG-I), a receptor of innate immunity that promotes type I interferon, was observed in perifascicular areas in DM. We compared the value of RIG-I expression with perifascicular atrophy as a biomarker of DM. Methods: We studied by immunohistochemical analysis the expression of RIG-I and the presence of perifascicular atrophy in 115 coded muscle biopsies: 44 patients with DM, 18 with myositis with overlap, 8 with ASS, 27 with non-DM inflammatory myopathy (16 with polymyositis, 6 with inclusion body myositis, 5 with immune-mediated necrotizing myopathy), 8 with muscular dystrophy (4 with dysferlinopathy, 4 with fascioscapulohumeral muscle dystrophy) and 10 healthy controls. Results: We found RIG-I-positive fibers in 50% of DM samples vs 11% in non-DM samples (p < 0.001). Interestingly, RIG-I staining identified 32% of DM patients without perifascicular atrophy (p = 0.007). RIG-I sensitivity was higher than perifascicular atrophy (p < 0.001). No differences in specificity between perifascicular atrophy and RIG-I staining were found (92% vs 88%). RIG-I staining was more reproducible than perifascicular atrophy (κ coefficient 0.52 vs 0.37). Conclusions: The perifascicular pattern of RIG-I expression supports the diagnosis of DM. Of importance for clinical and therapeutic studies, the inclusion of RIG-I in the routine pathological staining of samples in inflammatory myopathy will allow us to gather more homogeneous subgroups of patients in terms of immunopathogenesis. cc-by (c) Suárez Calvet, Xavier et al., 2017 http://creativecommons.org/licenses/by/3.0/es info:eu-repo/semantics/openAccess Dermatomiositis Marcadors bioquímics Dermatomyositis Biochemical markers RIG-I expression in perifascicular myofibers is a reliable biomarker of dermatomyositis info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion