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Myositis autoantibodies detected by line blot immunoassay: clinical associations and correlation with antibody signal intensity.
Loarce-Martos, Jesús; Calvo Sanz, Laura; Garrote-Corral, Sandra; Ballester González, Rubén; Pariente Rodríguez, Roberto; Rita, Claudia Geraldine; García-Soidan, Ana; Bachiller-Corral, Javier; Roy Ariño, Garbiñe.
Afiliación
  • Loarce-Martos J; Department of Rheumatology, Hospital Universitario Ramón y Cajal, Madrid, Spain. jesus.loarce@salud.madrid.org.
  • Calvo Sanz L; Department of Rheumatology, Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • Garrote-Corral S; Department of Rheumatology, Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • Ballester González R; Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • Pariente Rodríguez R; Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • Rita CG; Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • García-Soidan A; Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • Bachiller-Corral J; Department of Rheumatology, Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • Roy Ariño G; Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Rheumatol Int ; 43(6): 1101-1109, 2023 06.
Article en En | MEDLINE | ID: mdl-36763166
ABSTRACT
The aim of this study is to assess the relationship between myositis specific (MSA) and myositis associated (MAA) antibodies and diagnosis (including idiopathic inflammatory myopathies [IIM] and other systemic autoimmune diseases [SAID]), and to explore the impact of antibody signal intensity in diagnostic accuracy. We retrospectively reviewed all the serum samples obtained from patients tested for MSA/MAA by line immunoassay (LIA) between 01/01/2018 and 31/12/2020 in Ramón y Cajal University Hospital (Spain). Clinical true positive (CTP) MSAs and MAAs were defined as those patients with IIM or SAID with phenotypes expected of that MSA/MAA. Patients who did not have a phenotype compatible with that antibody were classified as clinical false positive (CFP). One hundred and thirty positive samples were analysed. Forty-six patients (33.38%) were classified as IIM, forty-two (32.3%) as SAID and forty-two (32.3%) as non-IIM/SAID. Among these 130 patients, 164 MSA/MAA were detected. Eighty-five (51.8%) positive MSA/MAA were classified as CTP, and seventy-nine (48.2%) as CFP. Strongly positive antibodies were more frequently CTP (35/47, 74.5%) than weak positives (54/68, 36.8%), (p ˂ 0.001). Antibodies classified as CTP had a higher signal intensity than CFP (36.77 AU vs 20.00 AU, CI95% 7.79-22.09, p ˂ 0.001). The probability of a CFP was associated to negative ANA, low ANA titer, and multiple positive MSA/MAA (p Ë‚ 0.001). In this study, we confirmed that CFP results using LIA are frequent, and are associated with low signal intensity MSA/MAA, negative ANA, lower titer ANA, and with multiple positive samples.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimiositis / Miositis Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Rheumatol Int Año: 2023 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimiositis / Miositis Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Rheumatol Int Año: 2023 Tipo del documento: Article País de afiliación: España