Treatment regimens for neuromyelitis optica spectrum disorder attacks: a retrospective cohort study

被引:39
作者
Demuth, Stanislas [1 ]
Guillaume, Maxime [2 ]
Bourre, Bertrand [2 ]
Ciron, Jonathan [3 ,4 ,15 ]
Zephir, Helene [5 ]
Sirejacob, Yoann [6 ]
Kerbrat, Anne [7 ]
Lebrun-Frenay, Christine [8 ]
Papeix, Caroline [9 ]
Michel, Laure [7 ,16 ,17 ]
Laplaud, David [10 ]
Vukusic, Sandra [11 ]
Maillart, Elisabeth [9 ]
Cohen, Mikael [8 ]
Audoin, Bertrand [12 ,13 ]
Marignier, Romain [14 ,18 ,19 ,20 ,21 ,22 ]
Collongues, Nicolas [1 ]
机构
[1] Strasbourg Univ Hosp, Dept Neurol, Strasbourg, France
[2] CHU Rouen, Rouen Univ Hosp, F-76000 Rouen, France
[3] CHU Toulouse, Dept Neurol, CRC SEP, F-31059 Toulouse 9, France
[4] Univ Toulouse III, Inst Toulousain Malad Infect & Inflammatoires Inf, INSERM, UMR1291,CNRS,UMR5051, Toulouse, France
[5] Univ Lille, Univ Hosp Lille, Dept Neurol, INSERM,U1172, Lille, France
[6] Rouen Univ Hosp, Dept Clin Res, F-76000 Rouen, France
[7] Rennes Univ Hosp, Dept Neurol, F-35033 Rennes, France
[8] Nice Cote dAzur Univ, Dept Neurol, CHU Nice, UR2CA,URRIS, Nice, France
[9] Hop La Pitie Salpetriere, AP HP, Dept Neurol, F-75013 Paris, France
[10] CHU Nantes, Serv Neurol, Nantes, France
[11] Hosp Civils Lyon, Dept Neurol, Hop Neurol, Bron, France
[12] Univ Hosp Marseille, Dept Neurol, Marseille, France
[13] Aix Marseille Univ, CNRS, CRMBM UMR 7339, Marseille, France
[14] Hop Wertheimer, HCL, Dept Neurol, Bron, France
[15] CHU Poitiers, Dept Neurol, F-86021 Poitiers, France
[16] CRTI, InsermU1064, Nantes, France
[17] Univ Nantes, CHU Nantes, Nantes, France
[18] Hosp Civils Lyon, Serv Neurol Sclerose Plaques Pathol Myeline & Neu, F-69677 Lyon, France
[19] Hosp Civils Lyon, Ctr Reference Malad Inflammatoires Rares Cerveau, F-69677 Lyon, France
[20] Ctr Neurosci Lyon, INSERM 1028, F-69003 Lyon, France
[21] Ctr Neurosci Lyon, UMR5292, CNRS, F-69003 Lyon, France
[22] Univ Claude Bernard Lyon 1, F-69000 Lyon, France
[23] Hop Neurol & Neurochirurg P Wertheimer, NeuroBioTec, 59 Blvd Pinel, Bron, France
关键词
Neuromyelitis optica; Therapeutics; MOGAD; Corticosteroids; Plasma exchanges; Relapses; PLASMA-EXCHANGE; IMPAIRMENT; HISTORY;
D O I
10.1186/s12974-022-02420-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Neuromyelitis optica spectrum disorder (NMOSD) attacks require an urgent probabilistic anti-inflammatory therapeutic strategy. As inadequately treated attacks result in disability, there is a need to identify the optimal attack-treatment regimen. Our study aimed to identify predictors of outcome after a first attack in patients with an NMOSD presentation and propose the best treatment strategy. Methods We performed a retrospective cohort study on the French national NMOSD registry (NOMADMUS), a nested cohort of the French multiple sclerosis observatory (OFSEP) recruiting patients with NMOSD presentations in France. We studied the first attack for any independent locations of clinical core characteristic of NMOSD, in treatment-naive patients. The primary outcome was the evolution of the Expanded Disability Status Scale (EDSS) score at 6 months, stratified in two ways to account for recovery (return to baseline EDSS score) and treatment response (classified as "good" if the EDSS score decreased by >= 1 point after a nadir EDSS score <= 3, or by >= 2 points after a nadir EDSS score > 3). We used ordinal logistic regression to infer statistical associations with the outcome. Results We included 211 attacks among 183 patients (104 with anti-AQP4 antibodies, 60 with anti-MOG antibodies, and 19 double seronegative). Attack treatment regimens comprised corticosteroids (n = 196), plasma exchanges (PE; n = 72) and intravenous immunoglobulins (n = 6). Complete recovery was reached in 40 attacks (19%) at 6 months. The treatment response was "good" in 134 attacks (63.5%). There was no improvement in EDSS score in 50 attacks (23.7%). MOG-antibody seropositivity and short delays to PE were significantly and independently associated with better recovery and treatment response. Conclusions We identified two prognostic factors: serostatus (with better outcomes among MOG-Ab-positive patients) and the delay to PE. We, therefore, argue for a more aggressive anti-inflammatory management of the first attacks suggesting an NMOSD presentation, with the early combination of PE with corticosteroids.
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