Ashida Shinji, Kondo Takayuki, Fujii Chihiro, Hamatani Mio, Mizuno Toshiki, Ochi Hirofumi
Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Department of Neurology, Kansai Medical University Medical Center, Osaka, Japan.
Front Neurol. 2022 Sep 20;13:1012857. doi: 10.3389/fneur.2022.1012857. eCollection 2022.
Multiple sclerosis (MS) is an immune-mediated demyelinating disease of the central nervous system. Without reliable diagnostic biomarkers, the clinical and radiological heterogeneity of MS makes diagnosis difficult. Although magnetic resonance imaging (MRI) is a major diagnostic tool for MS, the association of MRI findings with the inflammatory profile in cerebrospinal fluid (CSF) has been insufficiently investigated. Therefore, we focused on CSF profile of MS patients and examined its association with MRI findings.
Concentrations of 26 cytokines and chemokines were determined in CSF of 28 treatment-naïve MS patients and 12 disease-control patients with aquaporin-4 antibody-seropositive neuromyelitis optica spectrum disorder (NMOSD).
High levels of interleukin (IL)-6, IL-17A, B-cell activating factor (BAFF), a proliferation inducing ligand (APRIL), and CD40 ligand were correlated with the absence of at least one of the following three MRI findings in MS: an ovoid lesion, three or more periventricular lesions, and a nodular and/or ring-shaped contrast-enhancing lesion. The multivariate analysis revealed that elevated IL-17A was an independent predictor of absence of ovoid lesion and periventricular lesions less than three. MS patients were classified into a group with all three MRI findings (MS-full) and a group with less than three (MS-partial). The discriminant analysis model distinguished three groups: MS-full, MS-partial, and NMOSD, with 98% accuracy.
The CSF inflammatory profile was associated with radiological findings of treatment-naïve MS. This result indicates the possible utility of combined CSF and MRI profiling in identifying different MS phenotypes related to the heterogeneity of underlying immune processes.
多发性硬化症(MS)是一种中枢神经系统的免疫介导性脱髓鞘疾病。由于缺乏可靠的诊断生物标志物,MS的临床和影像学异质性使得诊断困难。尽管磁共振成像(MRI)是MS的主要诊断工具,但MRI表现与脑脊液(CSF)炎症特征之间的关联尚未得到充分研究。因此,我们聚焦于MS患者的CSF特征,并研究其与MRI表现的关联。
测定了28例未经治疗的MS患者和12例水通道蛋白4抗体血清阳性的视神经脊髓炎谱系障碍(NMOSD)疾病对照患者CSF中26种细胞因子和趋化因子的浓度。
高水平的白细胞介素(IL)-6、IL-17A、B细胞活化因子(BAFF)、增殖诱导配体(APRIL)和CD40配体与MS患者缺乏以下三种MRI表现中的至少一种相关:卵圆形病灶、三个或更多脑室周围病灶以及结节状和/或环形强化病灶。多变量分析显示,IL-17A升高是缺乏卵圆形病灶和少于三个脑室周围病灶的独立预测因素。MS患者被分为具有所有三种MRI表现的组(MS-全型)和少于三种表现的组(MS-部分型)。判别分析模型区分了三组:MS-全型、MS-部分型和NMOSD,准确率为98%。
CSF炎症特征与未经治疗的MS的影像学表现相关。这一结果表明,联合CSF和MRI分析在识别与潜在免疫过程异质性相关的不同MS表型方面可能具有实用性。