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Prevalence of Progression Independent of Relapse Activity and Relapse-Associated Worsening in Patients With Aqp4-Igg-Positive Nmosd Publisher Pubmed

Summary: Study finds progression without relapse is rare (2.2%) in AQP4-IgG NMOSD, with disability mostly from relapses. #NMOSD #Neurology

Siriratnam P1 ; Huda S1 ; Van Der Walt A1 ; Sanfilippo PG1 ; Sharmin S1 ; Foong YC1 ; Yeh WZ1 ; Zhu C1 ; Khoury SJ1 ; Csepany T1 ; Willekens B1 ; Etemadifar M1 ; Ozakbas S1 ; Nytrova P1 Show All Authors
Authors
  1. Siriratnam P1
  2. Huda S1
  3. Van Der Walt A1
  4. Sanfilippo PG1
  5. Sharmin S1
  6. Foong YC1
  7. Yeh WZ1
  8. Zhu C1
  9. Khoury SJ1
  10. Csepany T1
  11. Willekens B1
  12. Etemadifar M1
  13. Ozakbas S1
  14. Nytrova P1
  15. Altintas A1
  16. Alasmi A1
  17. Ramotello CM1
  18. Laureys G1
  19. Patti F1
  20. Horakova D1
  21. Foschi M1
  22. Boz C1
  23. Mccombe PA1
  24. Turkoglu R1
  25. Lechnerscott J1
  26. Roos I1
  27. Kalincik T1
  28. Jokubaitis VG1
  29. Butzkueven H1
  30. Monif M1

Source: Neurology Published:2024


Abstract

OBJECTIVES: In aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder (AQP4-IgG NMOSD), disability accrual is mostly attributed to relapses. This study aimed to assess the prevalence of progression independent of relapse activity (PIRA) and relapse-associated worsening (RAW) in AQP4-IgG NMOSD. METHODS: This was a retrospective cohort study of patients with AQP4-IgG NMOSD enrolled in the MSBase international data registry. Patients required a minimum of 3 recorded Expanded Disability Status Scale (EDSS) scores: baseline, event, and a 6-month confirmation score. Presence and absence of relapses between the baseline and event EDSS scores determined RAW and PIRA, respectively. Descriptive statistics were used to present the results. RESULTS: A total of 181 patients followed for a median of 4.5 years (Q1 1.7, Q3 7.8) were included. Most patients were female (88.4%), and the median age at disease onset was 38.1 years. Overall, 4 patients (2.2%) developed 5 incidences of PIRA and 13 patients developed RAW (7.2%). DISCUSSION: This multicenter study highlights that PIRA is very rare in AQP4-IgG NMOSD. Limitations of this study include the sole focus of overall EDSS to measure disability, lack of requirement for a second EDSS score to confirm baseline EDSS, and the absence of magnetic resonance imaging information for all patients.
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