Your browser doesn't support javascript.
loading
Positive Predictive Value of MOG-IgG for Clinically Defined MOG-AD Within a Real-World Cohort.
Manzano, Giovanna S; Salky, Rebecca; Mateen, Farrah J; Klawiter, Eric C; Chitnis, Tanuja; Levy, Michael; Matiello, Marcelo.
Afiliación
  • Manzano GS; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
  • Salky R; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
  • Mateen FJ; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
  • Klawiter EC; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
  • Chitnis T; Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Levy M; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
  • Matiello M; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Front Neurol ; 13: 947630, 2022.
Article en En | MEDLINE | ID: mdl-35795797
ABSTRACT
Myelin oligodendrocyte glycoprotein antibody associated disease (MOG-AD) is a CNS demyelinating disease, typically presenting with optic neuritis, transverse myelitis, and/or ADEM-like syndromes. The positive predictive value (PPV) of MOG-IgG testing by live cell-based assay was reported to be 72% in a study performed at the Mayo Clinic using a cut-off of 120. PPV may vary depending upon the tested population, thus supporting further investigation of MOG-IgG testing at other centers. In this real-world institutional cohort study, we determined the PPV of serum MOG-IgG for clinically defined MOG-AD in our patient population. The Massachusetts General Brigham Research Patient Data Registry database was queried for patients with positive serum MOG-IgG detection, at least once, between January 1, 2017 and March 25, 2021. All were tested via the MOG-IgG1 fluorescence-activated cell sorting assay (Mayo Laboratories, Rochester, MN). MOG-IgG positive cases were reviewed for fulfillment of typical MOG-AD clinical features, determined by treating neurologists and study authors. Of 1,877 patients tested, 78 (4.2%) patients tested positive for MOG-IgG with titer ≥120, and of these, 67 had validated MOG-AD yielding a PPV of 85.9%. Using a ≥140 titer cutoff, 65 (3.5%) tested positive and PPV was 93.8%. Three MOG positive cases had a prototypical multiple sclerosis diagnosis (RRMS n = 2, titers 120 and 140; PPMS n = 1; 1100). The treating diagnosis for one RRMS patient with a 140 titer was subsequently modified to MOG-AD by treating neurologists. Validated diagnoses of the remaining positive patients without MOG-AD included migraine (n = 2, titers 120, 1100), inclusion body myositis (n = 1, titer 1100), autoimmune encephalitis (n = 2, titers 120, 120), hypoxic ischemic brain injury (n = 1, titer 120), IgG4-related disease (n = 1, titer 120), and idiopathic hypertrophic pachymeningitis (n = 1, titer 120). In our cohort, the PPV for MOG-IgG improved utilizing a titer cut-off of ≥140. The presence of positive cases with and without demyelinating features, emphasizes a need for testing in the appropriate clinical context, analysis of titer value and clinical interpretation.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Neurol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Neurol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
...