Comparison of neutrophil-to-lymphocyte ratio between myelin oligodendrocyte glycoprotein antibody-associated disease and aquaporin-4 antibody-positive neuromyelitis optica spectrum disorders in adults

被引:4
|
作者
Duan, Zhenghao [1 ]
Feng, Juan [1 ,2 ]
机构
[1] Shengjing Hosp China Med Univ, Dept Neurol, Shenyang, Peoples R China
[2] Shengjing Hosp China Med Univ, Dept Neurol, 36 Sanhao St,Heping Dist, Shenyang 110004, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Myelin oligodendrocyte glycoprotein antibody; associated disease; Aquaporin-4; antibody; Neuromyelitis optica spectrum disorder; Complete blood count; Neutrophil-to-lymphocyte ratio;
D O I
10.1016/j.jocn.2022.05.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The neutrophil-to-lymphocyte ratio (NLR) is a biomarker for evaluating disease activity in systemic autoimmune diseases. However, few studies have discussed NLR changes in myelin oligodendrocyte glycoprotein antibody associated disease (MOGAD). This study aimed to explore the NLR difference between MOGAD, aquaporin-4 antibody (AQP4-Ab)-positive neuromyelitis optica spectrum disorders (NMOSD), and healthy controls (HCs) and evaluate the clinical value of NLR in the differential diagnosis. We included 15 patients with MOGAD, 28 patients with AQP4-Ab-positive NMOSD, and 68 HCs. Their NLRs were calculated, and statistical analysis was performed, with statistical significance set at P < 0.05. In pairwise comparisons between three groups, P < 0.017 was considered statistically significant under Bonferroni correction. NLR was higher during the acute attack in MOGAD patients than HCs but lower than in AQP4-Ab-positive NMOSD patients. NLR was correlated with Expanded Disability Status Scale (EDSS) in MOGAD and AQP4-Ab-positive NMOSD patients. Also, there were no statistical differences in intracranial pressure between MOGAD and AQP4-Ab-positive NMOSD patients and HCs. The cut-off value was 2.86, and the sensitivity and specificity were 0.750 and 0.867, respectively. In conclusion, our results suggest that NLR may be a helpful marker to evaluate disease severity and differentiate between both diseases at a cut-off value of > 2.86 when patients have clinical symptoms like optic neuritis or myelitis.
引用
收藏
页码:89 / 93
页数:5
相关论文
共 50 条
  • [1] Pathology of myelin oligodendrocyte glycoprotein antibody-associated disease: a comparison with multiple sclerosis and aquaporin 4 antibody-positive neuromyelitis optica spectrum disorders
    Takai, Yoshiki
    Misu, Tatsuro
    Fujihara, Kazuo
    Aoki, Masashi
    FRONTIERS IN NEUROLOGY, 2023, 14
  • [2] Aquaporin 4 antibody-positive neuromyelitis optica spectrum disorders and myelin oligodendrocyte glycoprotein antibody-associated encephalomyelitis. A brief review
    Jarius, Sven
    Wildemann, Brigitte
    NERVENARZT, 2021, 92 (04): : 317 - 333
  • [3] Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-Associated CNS Demyelination: Clinical Spectrum and Comparison with Aquaporin-4 Antibody Positive Neuromyelitis Optica Spectrum Disorder
    Ojha, Pawan T.
    Aglave, Vikram B.
    Soni, Girish
    Jagiasi, Kamlesh A.
    Singh, Rakesh K.
    Singh, Rakeshsingh Kamleshsingh
    Nagendra, Shashank
    NEUROLOGY INDIA, 2020, 68 (05) : 1106 - 1114
  • [4] Seizures and epilepsy in multiple sclerosis, aquaporin 4 antibody-positive neuromyelitis optica spectrum disorder, and myelin oligodendrocyte glycoprotein antibody-associated disease
    Li, Er-Chuang
    Zheng, Yang
    Cai, Meng-Ting
    Lai, Qi-Lun
    Fang, Gao-Li
    Du, Bing-Qing
    Shen, Chun-Hong
    Zhang, Yin-Xi
    Wu, Long-Jun
    Ding, Mei-Ping
    EPILEPSIA, 2022, 63 (09) : 2173 - 2191
  • [5] Myelin Oligodendrocyte Glycoprotein Antibody-associated Neuromyelitis optica spectrum disorders (NMOSD)
    Khan, F. M.
    Dave, D.
    Nirhale, S.
    Rohatgi, S.
    Rao, P.
    Naphade, P.
    EUROPEAN JOURNAL OF NEUROLOGY, 2020, 27 : 924 - 924
  • [6] Neurite orientation dispersion and density imaging and multiparameter mapping in aquaporin-4 antibody positive neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein antibody-associated disease
    Chen, Qianlan
    Trang, Henri
    Mewes, Darius
    Chien, Claudia
    Schindler, Patrick
    Rust, Rebekka
    Hartung, Tim
    Finke, Carsten
    Schmitz-Huebsch, Tanja
    Hetzer, Stefan
    Brandt, Alexander U.
    Paul, Friedemann
    MULTIPLE SCLEROSIS JOURNAL, 2023, 29 : 513 - 514
  • [7] Neuromyelitis optica spectrum disorders and myelin oligodendrocyte glycoprotein antibody-associated disease: current topics
    Fujihara, Kazuo
    Cook, Lawrence J.
    CURRENT OPINION IN NEUROLOGY, 2020, 33 (03) : 300 - 308
  • [8] Optic chiasm involvement in multiple sclerosis, aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein-associated disease
    Bianchi, Alessia
    Cortese, Rosa
    Prados, Ferran
    Tur, Carmen
    Kanber, Baris
    Yiannakas, Marios C.
    Samson, Rebecca
    De Angelis, Floriana
    Magnollay, Lise
    Jacob, Anu
    Brownlee, Wallace
    Trip, Anand
    Nicholas, Richard
    Hacohen, Yael
    Barkhof, Frederik
    Ciccarelli, Olga
    Toosy, Ahmed T.
    MULTIPLE SCLEROSIS JOURNAL, 2024, 30 (06) : 674 - 686
  • [9] Increased peripheral inflammatory responses in myelin oligodendrocyte glycoprotein associated disease and aquaporin-4 antibody positive neuromyelitis optica spectrum disorder
    Bauer, A.
    Rudzki, D.
    Berek, K.
    Dinoto, A.
    Lechner, C.
    Wendel, E. -M.
    Hegen, H.
    Deisenhammer, F.
    Berger, T.
    Hoeftberger, R.
    Rostasy, K.
    Mariotto, S.
    Reindl, M.
    MULTIPLE SCLEROSIS JOURNAL, 2022, 28 (3_SUPPL) : 43 - 44
  • [10] Increased peripheral inflammatory responses in myelin oligodendrocyte glycoprotein associated disease and aquaporin-4 antibody positive neuromyelitis optica spectrum disorder
    Bauer, Angelika
    Rudzki, Dagmar
    Berek, Klaus
    Dinoto, Alessandro
    Lechner, Christian
    Wendel, Eva-Maria
    Hegen, Harald
    Deisenhammer, Florian
    Berger, Thomas
    Hoeftberger, Romana
    Rostasy, Kevin
    Mariotto, Sara
    Reindl, Markus
    FRONTIERS IN IMMUNOLOGY, 2022, 13