Nicolescu Mihaela, Häußler Vivien, Paul Friedemann, Oertel Frederike Cosima, Schindler Patrick, Strobl Judith Bellmann, Krumbholz Markus, Hümmert Martin W, Bütow Franziska, Tkachenko Daria, Trebst Corinna, Schubert Charlotte, Ayzenberg Ilya, Schwake Carolin, Pakeerathan Thivya, Fischer Katinka, Aktas Orhan, Ringelstein Marius, Kraemer Markus, Warnke Clemens, Grothe Matthias, Kaste Matthias, Angstwurm Klemens, Kern Peter, Kleiter Ingo, Rommer Paulus, Winkelmann Alexander, Walter Annette, Weber Martin S, Wickel Jonathan, Giglhuber Katrin, Then Bergh Florian, Senel Makbule, Tumani Hayrettin, Vardakas Ioannis, Dawin Eva, Revie Lisa, Klotz Luisa, Korporal-Kuhnke Mirjam, Jarius Sven, Wildemann Brigitte, Gernert Jonathan A, Kümpfel Tania, Engels Daniel, Havla Joachim, Stolowy Natacha, Stellmann Jan-Patrick
APHM, Hôpital de la Timone, CEMEREM, Marseille, France.
Aix Marseille University, CNRS, CRMBM, Marseille, France.
J Neurol. 2024 Dec 21;272(1):86. doi: 10.1007/s00415-024-12803-5.
In this multicentric study, we were interested in the vision-related quality of life and its association with visual impairment in neuromyelitis optica spectrum disorders (NMOSD) and myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) in comparison to multiple sclerosis (MS) and healthy controls.
We analysed extracted data from the German NEMOS registry including National Eye Institute Visual Function Questionnaire (NEI-VFQ) scores, high and low contrast visual acuity (HCVA, LCVA), visually evoked potentials (VEP) and the scores for the expanded disability status scale (EDSS) and other neurological tests which assessed their disease-related impairment. The mean follow-up time of our patients was 1.2 years. We used adjusted linear mixed effect models to analyse NEI-VFQ differences and interactions with visual acuity among NMOSD, MOGAD, a matched MS cohort and healthy controls.
Despite a younger age in the MOGAD cohort (39 y.o.), vision and socioemotional-related quality of life reduction was similar over all patient subgroups in comparison to healthy controls. The most impacted life quality dimension was general health, followed by general vision, driving and role difficulties. Decline in some of the NEI-VFQ subscales scores is mostly predicted by age. The HCVA was the best predictor for most of the subscales of the NEI-VFQ.
Despite important age differences, NMOSD, MOGAD and MS seem to share a rather similar perception on their vision and quality of life impairment, which is overall poorer than that of healthy controls.
在这项多中心研究中,我们关注视神经脊髓炎谱系障碍(NMOSD)和髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)与多发性硬化症(MS)及健康对照相比,与视力相关的生活质量及其与视力损害的关联。
我们分析了从德国NEMOS注册中心提取的数据,包括美国国立眼科研究所视觉功能问卷(NEI-VFQ)评分、高对比度和低对比度视力(HCVA、LCVA)、视觉诱发电位(VEP)以及扩展残疾状态量表(EDSS)评分和其他评估其疾病相关损害的神经学测试。我们患者的平均随访时间为1.2年。我们使用调整后的线性混合效应模型来分析NMOSD、MOGAD、匹配的MS队列和健康对照之间NEI-VFQ的差异以及与视力的相互作用。
尽管MOGAD队列患者年龄较轻(39岁),但与健康对照相比,所有患者亚组的视力和社会情感相关生活质量下降情况相似。受影响最大的生活质量维度是总体健康,其次是总体视力、驾驶和角色困难。NEI-VFQ某些子量表评分的下降大多由年龄预测。HCVA是NEI-VFQ大多数子量表的最佳预测指标。
尽管存在重要的年龄差异,但NMOSD、MOGAD和MS在视力和生活质量损害方面似乎有相当相似的认知,总体上比健康对照差。