Comparison of clinical and laboratory characteristics of neuromyelitis optica spectrum disorder with or without anti-connective tissue antibodies: an 18-month cohort follow-up - Report - MDSpire

Comparison of clinical and laboratory characteristics of neuromyelitis optica spectrum disorder with or without anti-connective tissue antibodies: an 18-month cohort follow-up

  • By

  • Shuna Shi

  • Yang Liu

  • Zhenling Fu

  • Junzhe Yang

  • Zhengyu Sun

  • Haiyang Luo

  • Limei Wang

  • Yuming Xu

  • June 19, 2026

  • 0 min

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Clinical Report: Evaluation of Clinical and Laboratory Features in NMOSD

Overview

This study evaluates the role of anti-connective tissue antibodies in neuromyelitis optica spectrum disorder (NMOSD) by analyzing clinical and laboratory data from 205 patients. Findings indicate that CTD abs positivity is associated with a more severe inflammatory profile but does not predict earlier relapse.

Background

Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune condition affecting the central nervous system, primarily driven by aquaporin-4 antibodies. Understanding the role of anti-connective tissue antibodies in NMOSD is crucial, as their presence may influence disease characteristics. Previous studies have shown inconsistent results regarding the impact of these antibodies on disease activity.

Data Highlights

VariableCTD abs+ (n=108)CTD abs− (n=97)p-value
Lymphocyte counts1.82 ± 0.141.73 ± 0.07< 0.01
Monocyte-to-lymphocyte ratio0.27 (0.2)0.24 (0.16)0.037
CSF white blood cell counts10 (22)6 (18)0.035
Oligoclonal band positivity27.78%10.31%0.002
24-hour intrathecal IgG synthesis rate54.6%40.2%0.039
CSF immunoglobulin levels5.755 (6.37) mg/dL4.15 (3.53) mg/dL< 0.001

Key Findings

  • 52.7% of patients were positive for anti-connective tissue antibodies (CTD abs+).
  • CTD abs+ patients had higher lymphocyte counts compared to CTD abs− patients (1.82 vs. 1.73, p < 0.01).
  • Higher monocyte-to-lymphocyte ratios were observed in the CTD abs+ group (0.27 vs. 0.24, p = 0.037).
  • CTD abs+ patients exhibited higher CSF white blood cell counts (10 vs. 6/106/L, p = 0.035).
  • Oligoclonal band positivity was significantly higher in the CTD abs+ group (27.78% vs. 10.31%, p = 0.002).
  • CTD abs+ patients had higher Expanded Disability Status Scale scores at first relapse.

Clinical Implications

The presence of anti-connective tissue antibodies in NMOSD patients may indicate a more severe inflammatory profile. However, these antibodies do not appear to predict earlier relapses.

Conclusion

The study highlights the association between anti-connective tissue antibodies and increased inflammatory markers in NMOSD, while also clarifying that these antibodies do not predict earlier relapses.

Related Resources & Content

  1. Acta Neuropathologica, 2020 -- Pathological Insights into Inflammatory Demyelinating Disorders of the Central Nervous System Associated with Myelin Oligodendrocyte Glycoprotein Autoantibodies
  2. Frontiers in Medicine, 2026 -- Neuromyelitis optica spectrum disorder with painful tonic spasms as the first symptom: a case report
  3. Frontiers in Oncology, 2026 -- Case Report: Neuromyelitis optica spectrum disorder associated with gastric cardia and pancreatic cancers: clinical features and oncological implications
  4. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders - PMC
  5. Eculizumab in Aquaporin-4–Positive Neuromyelitis Optica Spectrum Disorder | New England Journal of Medicine
  6. Frontiers in Immunology — Case Report: Presenting as optic neuritis—a biopsy-proven IgG4 anti-NF155–positive combined central and peripheral demyelination syndrome
  7. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders - PMC
  8. Eculizumab in Aquaporin-4–Positive Neuromyelitis Optica Spectrum Disorder | New England Journal of Medicine
  9. Clinical features and prognosis of NMOSD patients with positive autoimmune antibodies

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