White blood cell count profiles in anti-aquaporin-4 antibody seropositive neuromyelitis optica spectrum disorder and anti-myelin oligodendrocyte glycoprotein antibody-associated disease

医学 白细胞 视神经脊髓炎 免疫学 多发性硬化 病理 胃肠病学 全血细胞计数 内科学
作者
Tetsuya Akaishi,Tatsuro Misu,Kazuo Fujihara,Kumi Nakaya,Naoki Nakaya,Tomohiro Nakamura,Mana Kogure,Rieko Hatanaka,Fumi Itabashi,Ikumi Kanno,Kimihiko Kaneko,Toshiyuki Takahashi,Juichi Fujimori,Yoshiki Takai,Shuhei Nishiyama,Tadashi Ishii,Masashi Aoki,Ichiro Nakashima,Atsushi Hozawa
出处
期刊:Scientific Reports [Nature Portfolio]
卷期号:13 (1) 被引量:7
标识
DOI:10.1038/s41598-023-33827-3
摘要

White blood cell (WBC) count profiles in anti-aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder (AQP4-NMOSD) and anti-myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) are still unknown. This study evaluated the total WBC count, differential WBC counts, monocyte-to-lymphocyte ratio (MLR), and neutrophil-to-lymphocyte ratio (NLR) in patients with these diseases within three months from an attack before acute treatment or relapse prevention and compared the profiles with those in matched volunteers or in multiple sclerosis (MS) patients. AQP4-NMOSD patients (n = 13) had a higher neutrophil count (p = 0.0247), monocyte count (p = 0.0359), MLR (p = 0.0004), and NLR (p = 0.0037) and lower eosinophil (p = 0.0111) and basophil (p = 0.0283) counts than those of AQP4-NMOSD-matched volunteers (n = 65). Moreover, patients with MOGAD (n = 26) had a higher overall WBC count (p = 0.0001), neutrophil count (p < 0.0001), monocyte count (p = 0.0191), MLR (p = 0.0320), and NLR (p = 0.0002) than those of MOGAD-matched volunteers (n = 130). The three demyelinating diseases showed similar levels of the total and differential WBC counts; however, MOGAD and MS showed different structures in the hierarchical clustering and distributions on a two-dimensional canonical plot using differential WBC counts from the other three groups. WBC count profiles were similar in patients with MOGAD and MS but differed from profiles in matched volunteers or patients with AQP4-NMOSD.
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