Limited early IVIG for the treatment of pediatric myelin oligodendrocyte glycoprotein antibody-associated disease.

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Tác giả: Aaron Abrams, Leslie Benson, Theron Charles Casper, Tanuja Chitnis, Mark Gorman, Rebecca MacRae, Soe Mar, Jayne Ness, Kimberly O'Neill, Jonathan Race, Mary Rensel, Moses Rodriguez, John Rose, Vinicius Schoeps, Allison Schuette, Nikita Shukla, Akash Virupakshaiah, Michael Waltz, Emmanuelle Waubant, Yolanda Wheeler

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: Netherlands : Multiple sclerosis and related disorders , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 713651

BACKGROUND AND OBJECTIVES: This study aimed to evaluate whether a 6-month (limited) course of early IVIG is an effective strategy for relapse prevention in children with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) versus only acute therapies or other early immunotherapies. METHODS: This was a retrospective multicenter observational study of pediatric MOGAD patients from the US Network of Pediatric Multiple Sclerosis Centers with disease onset between October 1996 and December 2022. Controls were matched to limited early IVIG subjects using a 3:1 ratio. Hazard ratios of time to relapse and rate ratios of annualized relapse rate were calculated. The cumulative probability of remaining relapse-free was evaluated with the Kaplan-Meier method. RESULTS: We identified 130 unique control subjects treated before second attack with acute treatments only used in matching, 18 subjects treated with limited early IVIG, and 23 subjects treated with other early immunotherapy. The time to relapse was not different between either the limited early IVIG group and control group (HR 0.60 [0.22, 1.66], p = 0.32) or other early immunotherapy group (HR 0.98 [0.27, 3.6], p = 0.98). The limited early IVIG group showed a lower annualized relapse rate, although not statistically significant (RR 0.44 [0.17, 1.14], p = 0.09) compared with controls and a similar annualized relapse rate compared with the other early immunotherapy group (RR 0.56 [0.19, 1.69], p = 0.30). DISCUSSION: Although underpowered, our results suggest that the use of a limited, 6-month course of early IVIG may reduce the risk of multiphasic disease in pediatric MOGAD.
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