Prevalence of Progression Independent of Relapse Activity and Relapse-Associated Worsening in Patients With AQP4-IgG-Positive NMOSD.

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY
Neurology Pub Date : 2024-12-24 Epub Date: 2024-11-19 DOI:10.1212/WNL.0000000000209940
Pakeeran Siriratnam, Saif Huda, Anneke Van Der Walt, Paul G Sanfilippo, Sifat Sharmin, Yi Chao Foong, Wei Z Yeh, Chao Zhu, Samia J Khoury, Tunde Csepany, Barbara Willekens, Masoud Etemadifar, Serkan Ozakbas, Petra Nytrova, Ayse Altintas, Abdullah Al-Asmi, Cristina M Ramo-Tello, Guy Laureys, Francesco Patti, Dana Horakova, Matteo Foschi, Cavit Boz, Pamela A Mccombe, Recai Turkoglu, Jeannette Lechner-Scott, Izanne Roos, Tomas Kalincik, Vilija G Jokubaitis, Helmut Butzkueven, Mastura Monif
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引用次数: 0

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.

与 AQP4-IgG 阳性 NMOSD 患者的复发活动和复发相关恶化无关的病情进展发生率。
目的:在水光素-4抗体阳性的神经脊髓炎视网膜频谱障碍(AQP4-IgG NMOSD)患者中,残疾的增加主要归因于复发。本研究旨在评估独立于复发活动的进展(PIRA)和复发相关恶化(RAW)在AQP4-IgG NMOSD中的患病率:这是一项回顾性队列研究,研究对象是MSBase国际数据登记处登记的AQP4-IgG NMOSD患者。患者需要至少3次有记录的残疾状况扩展量表(EDSS)评分:基线评分、事件评分和6个月的确认评分。基线和事件 EDSS 评分之间有无复发分别决定了 RAW 和 PIRA。结果采用描述性统计:共纳入 181 名患者,随访时间中位数为 4.5 年(Q1 1.7,Q3 7.8)。大多数患者为女性(88.4%),发病年龄中位数为 38.1 岁。总体而言,4 名患者(2.2%)出现了 5 次 PIRA,13 名患者出现了 RAW(7.2%):这项多中心研究表明,PIRA 在 AQP4-IgG NMOSD 中非常罕见。本研究的局限性包括:仅以总体 EDSS 来衡量残疾程度,未要求进行第二次 EDSS 评分以确认基线 EDSS,以及所有患者均未提供磁共振成像信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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