免疫疗法抵抗神经性疼痛和疲劳预测接触相关蛋白样2抗体疾病的生活质量。

IF 8.1 1区 医学 Q1 CLINICAL NEUROLOGY
Bryan Ceronie, Christine Strippel, Christopher Uy, Sofija Paneva, Mateusz Makuch, Babak Soleimani, Sanchit Turaga, Sophie Binks, Sudarshini Ramanathan, Sophia Michael, James Varley, Ava Easton, Andreas Themistocleous, John Dawes, David L Bennett, Anushka Irani, Adam E Handel, Sarosh R Irani
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引用次数: 0

摘要

接触相关蛋白样2 (CASPR2)抗体疾病的长期临床结果和相关预后因素尚不清楚。共有75名携带CASPR2抗体的参与者进行了残疾、生活质量和慢性疼痛的纵向评估。虽然大多数症状在治疗6个月内得到改善,但神经性疼痛和疲劳是免疫治疗最难治性的,并持续长达6年。此外,这两个因素——而不是CASPR2抗体水平或亚型——独立地预测了24个月时更严重的残疾和生活质量。对于任何给定的修正兰金量表评分,生活质量差异很大,表明患者和临床医生评估结果之间存在分歧。进一步的工作应该研究这些措施的相对重要性,以及顽固性症状的免疫发病机制。Ann neurol 2025。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunotherapy-Resistant Neuropathic Pain and Fatigue Predict Quality-of-Life in Contactin-Associated Protein-Like 2 Antibody Disease.

The long-term clinical outcomes and associated prognostic factors in contactin-associated protein-like 2 (CASPR2)-antibody diseases are unknown. A total of 75 participants with CASPR2 antibodies were longitudinally assessed for disability, quality-of-life, and chronic pain. Although most symptoms improved within 6 months of treatment, neuropathic pain and fatigue were the most immunotherapy refractory, and persisted for up to 6 years. Furthermore, these two factors-but not CASPR2 antibody levels or subclasses-independently predicted worse disability and quality-of-life at 24 months. Quality-of-life varied widely for any given modified Rankin Scale score, indicating a divergence between patient and clinician assessed outcomes. Further work should study the relative importance of these measures, and the immunopathogenesis underlying intractable symptoms. ANN NEUROL 2025.

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来源期刊
Annals of Neurology
Annals of Neurology 医学-临床神经学
CiteScore
18.00
自引率
1.80%
发文量
270
审稿时长
3-8 weeks
期刊介绍: Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.
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