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

To explore the significance of anti-connective tissue antibodies in the clinical diagnosis and evaluation of neuromyelitis optica spectrum disorder (NMOSD).

Approach:
    Key Findings:
    • Among the 205 patients, 108 (52.7%) were positive for anti-connective tissue antibodies (CTD abs+).
    • Compared with CTD abs− patients, the CTD abs+ group had higher lymphocyte counts, higher monocyte-to-lymphocyte ratios, higher CSF white blood cell counts, and higher CSF immunoglobulin levels.
    • CTD abs+ patients exhibited a higher rate of oligoclonal band positivity and a higher proportion with increased 24-hour intrathecal IgG synthesis rate.
    • No significant differences in lesion distribution or length of affected spinal cord segments were observed between the two groups.
    • CTD abs+ patients had higher Expanded Disability Status Scale scores at first relapse and a higher annualized relapse rate over the 18-month follow-up.
    Interpretation:

    Limitations:
    • The study was limited to patients with AQP4-IgG positivity and did not include those with other CNS demyelinating diseases or diagnosed connective tissue diseases.
    Conclusion:

    CTD abs positivity in AQP4-IgG-positive NMOSD patients does not predict earlier relapses.

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