Literature DB >> 36166174

Disability outcomes in NMOSD and MOGAD patients: data from a nationwide registry in Argentina.

Juan I Rojas1,2,3, Agustín Pappolla4, Liliana Patrucco5, Edgardo Cristiano5, Jimena Miguez4, Susana Liwacki6,7, Verónica Tkachuk8, María E Balbuena8, Carlos Vrech9, Norma Deri10, Jorge Correale11, Mariano Marrodan11, María C Ysrraelit11, Marcela Fiol11, Felisa Leguizamon12, Geraldine Luetic13, María L Menichini14, Pablo A Lopez15, Juan Pablo Pettinicchi15, Juan Criniti15, Alejandro Caride15, Darío Tavolini16, Carolina Mainella17, Gisela Zanga18, Marcos Burgos19, Javier Hryb20, Andrés Barboza21, Luciana Lazaro22, Ricardo Alonso23,22, Berenice Silva23, Nora Fernández Liguori22, Débora Nadur8,24, Aníbal Chercoff25, Alejandra Martinez25, Judith Steinberg25, Orlando Garcea23, Adriana Carrá25, Marina Alonso Serena26, Edgar Carnero Contentti15.   

Abstract

The objective was to evaluate time to reach an EDSS of 4, 6, and 7 in NMOSD and MOGAD patients included in the Argentinean MS and NMOSD registry (RelevarEM, NCT 03,375,177).
METHODS: NMOSD patients diagnosed according to 2015 criteria and with MOGAD were identified. Patients with at least 3 years of follow-up and periodic clinical evaluations with EDSS outcomes were included. AQP4-antibody and MOG-antibody status was recorded, and patients were stratified as seropositive and seronegative for AQP4-antibody. EDSS of 4, 6, and 7 were defined as dependent variables. Log rank test was used to identify differences between groups.
RESULTS: Registry data was provided for a total of 137 patients. Of these, seventy-five presented AQP4-ab-positive NMOSD, 45 AQP4-ab-negative NMOSD, and 11 MOGAD. AQP4-ab status was determined by cell-based assay (CBA) in 72% of NMOSD patients. MOG-ab status was tested by CBA in all cases. Mean time to EDSS of 4 was 53.6 ± 24.5 vs. 63.1 ± 32.2 vs. 44.7 ± 32 months in seropositive, seronegative NMOSD, and MOGAD, respectively (p = 0.76). Mean time to EDSS of 6 was 79.2 ± 44.3 vs. 75.7 ± 48.6 vs. 54.7 ± 50 months in seropositive, seronegative NMOSD, and MOGAD (p = 0.23), while mean time to EDSS of 7 was 86.8 ± 54 vs. 80.4 ± 51 vs. 58.5 ± 47 months in seropositive, seronegative NMOSD, and MOGAD (p = 0.39).
CONCLUSION: No differences were observed between NMOSD (seropositive and seronegative) and MOGAD in survival curves.
© 2022. Fondazione Società Italiana di Neurologia.

Entities:  

Keywords:  Disability; Epidemiology; MOGAD; NMOSD

Year:  2022        PMID: 36166174     DOI: 10.1007/s10072-022-06409-w

Source DB:  PubMed          Journal:  Neurol Sci        ISSN: 1590-1874            Impact factor:   3.830


  1 in total

1.  Assessing attacks and treatment response rates among adult patients with NMOSD and MOGAD: Data from a nationwide registry in Argentina.

Authors:  Edgar Carnero Contentti; Pablo A Lopez; Juan Pablo Pettinicchi; Juan Criniti; Agustín Pappolla; Jimena Miguez; Liliana Patrucco; Edgardo Carnero Contentti; Susana Liwacki; Verónica Tkachuk; María E Balbuena; Carlos Vrech; Norma Deri; Jorge Correale; Mariano Marrodan; María C Ysrraelit; Felisa Leguizamon; Geraldine Luetic; María L Menichini; Darío Tavolini; Carolina Mainella; Gisela Zanga; Marcos Burgos; Javier Hryb; Andrés Barboza; Luciana Lazaro; Ricardo Alonso; Nora Fernández Liguori; Débora Nadur; Aníbal Chercoff; Marina Alonso Serena; Alejandro Caride; Friedemann Paul; Juan I Rojas
Journal:  Mult Scler J Exp Transl Clin       Date:  2021-08-20
  1 in total

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