Skip to content
Review Open access

Global trends and emerging hotspots in neuromyelitis optica spectrum disorder diagnostic research

Aug 2026 · Medicine · Vol 105, pp. e50424 · 0 citations · 49 references
Medicine

TL;DR

NMOSD diagnostic research has transitioned from consensus-driven classification toward integrated, multimodal precision strategies, and co-citation and keyword analyses demonstrated a clear shift from an early focus on disease definition and differential diagnosis toward biomarker-guided and technology-enabled precision diagnosis.

Abstract

Background: Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune inflammatory disease of the central nervous system characterized by recurrent optic neuritis and longitudinally extensive transverse myelitis, frequently leading to severe and irreversible disability. Over the past decade, advances in diagnostic criteria, serological testing, and biomarker research have substantially transformed the diagnostic framework of NMOSD. However, a comprehensive bibliometric analysis focusing specifically on diagnostic research in this field has been lacking. Methods: Publications related to NMOSD diagnostic research published between 2016 and 2025 were retrieved from the Web of Science Core Collection. After refinement of the search strategy and manual screening based on predefined relevance criteria, bibliometric analyses were performed using CiteSpace, VOSviewer, and the Bibliometrix package in R to evaluate publication trends, international collaboration patterns, co-citation networks, and evolving research hotspots. Results: A total of 2029 publications were included. Annual publication output and citation counts increased steadily throughout the study period, reflecting sustained expansion of academic interest. China was the leading contributor, with strong collaborative links to the United States and the United Kingdom. The 2015 international consensus diagnostic criteria emerged as the most influential reference, serving as a foundational framework for subsequent research. Co-citation and keyword analyses demonstrated a clear shift from an early focus on disease definition and differential diagnosis toward biomarker-guided and technology-enabled precision diagnosis. Current research frontiers include optimization of aquaporin-4 immunoglobulin G detection platforms, astrocytic injury biomarkers such as glial fibrillary acidic protein, inflammatory mediators including interleukin-6 and complement components, magnetic resonance imaging– and optical coherence tomography–based neuroimaging markers, and multimodal diagnostic assessment. Conclusion: NMOSD diagnostic research has transitioned from consensus-driven classification toward integrated, multimodal precision strategies. Continued international collaboration and biomarker standardization will be essential to improve early diagnosis and clinical management.

Read PDF

Similar papers

Open access Aug 2026

Diagnostic features of the neuromyelitis optica spectrum disorders in real clinical practice

Four clinical cases of NMOSD that illustrate the difficulties in making a timely diagnosis due to an ambiguous clinical, radiological and laboratory picture were presented and strategies to improve the early diagnosis of NMOSD to prevent such outcomes were proposed.

K. Bakhtiyarova, O. V. Lyutov, T. R. Galiullin et al. · 0 citations
Open access Aug 2026

Neuromyelitis Optica Stabilized through Dharma

The case of a woman with a history of NMOSD spanning more than 30 years who experienced sustained clinical stability after adopting the Five Golden Buddhist Practices of Guan Yin Citta Dharma Door suggests that Dharma-based spiritual practices may offer potential benefits as a complementary approach for some individual...

Xing-Hong Yang · 0 citations
Review Open access Sep 2026

Prevalence of autoimmune comorbidities in aquaporin 4-immunoglobulin G positive neuromyelitis optica spectrum disorder: a systematic review and meta-analysis.

BACKGROUND Autoimmune comorbidities in aquaporin-4-immunoglobulin G (AQP4-IgG)-positive neuromyelitis optica spectrum disorder (NMOSD) may be associated with increased disease severity and therapeutic challenges, yet prevalence estimates vary considerably. Some variability may reflect differences in population characte...

Ning-Lu Weng, Aikjot Randhawa, Karen Sayfee et al. · 0 citations
Open access Sep 2026

Inflammatory and immune pathways in Ménière’s disease: a multi-database bibliometric and visualized analysis of research trends

Ménière’s disease (MD) is a chronic inner ear disorder characterized by recurrent episodes of vertigo, fluctuating sensorineural hearing loss, tinnitus, and aural fullness. Growing evidence indicates that aberrant immune regulation, inflammation, and allergic reactions are involved in the development of MD. However...

Ying-Fu Zhou, Jia-Hui Xiong, Yong Huang et al. · 0 citations
Review Open access Oct 2026

Ravulizumab in neuromyelitis optica spectrum disorder: first clinical experience in Chile

Neuromyelitis optica spectrum disorder (NMOSD) is a neuroimmunological astrocytopathy mediated by anti-aquaporin-4 (AQP4-IgG) antibodies that trigger complement-dependent cytotoxicity and activation of the terminal complement cascade in the central nervous system. Ravulizumab, a long-acting terminal complement C5 i...

T. Santibáñez, J. M. Valdés, C. Romero et al. · 0 citations
Aug 2026

Age-stratified clinical characteristics and disability outcomes in neuromyelitis optica spectrum disorder: A cross-sectional study.

Age at diagnosis may represent a relevant clinical factor when evaluating disability burden in NMOSD and further prospective multicenter studies are warranted to better define longitudinal outcomes and prognostic factors in LO-NMOSD.

O. Mirmosayyeb, Mehra Fekri, Mohammad Yazdan Panah et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.