Neuro-Immunology Service and Department of Neurology (I.L., M.A.H.), Rabin Medical Center; Department of Neurology (I.L., F.B., R.M., M.A.H., I.S.), Rabin Medical Center; and Sackler Faculty of Medicine (I.L., F.B., R.M., M.A.H., I.S.), Tel Aviv University, Israel.
Neurol Neuroimmunol Neuroinflamm. 2019 Jun 18;6(5):e584. doi: 10.1212/NXI.0000000000000584. eCollection 2019 Sep.
MS is a demyelinating CNS disorder with a spectrum of clinical patterns regarding course and prognosis. Although several prognostic factors are considered in the initial evaluation of patients, biological markers defining the disease course and guiding treatments are currently lacking. It is unknown whether patients with CSF pleocytosis differ in regard to symptoms, disease course, and prognosis from those without. The aim of this study was to evaluate whether CSF pleocytosis during the initial presentation has an impact on the clinical course and progression of MS.
We retrospectively evaluated patients attending the MS Clinic at Rabin Medical Center between January 1999 and January 2016 who underwent lumbar puncture (LP) at disease presentation, considering CSF cell count, clinical diagnosis (clinically isolated syndrome [CIS] and relapsing-remitting MS [RRMS]), annualized relapse rate (ARR), paraclinical findings (imaging, CSF oligoclonal bands, and evoked potentials), and disease progression, expressed by the Expanded Disability Status Scale (EDSS).
One hundred fourteen patients (72 females) underwent LP at disease presentation (RRMS: n = 100, CIS: n = 14). Age at diagnosis was 32.4 ± 12.2 years, and the follow-up time was 9.4 ± 3.8 years. Forty-six patients showed a pleocytic CSF (≥5 cells per μL). Compared with patients with <4 cells per μL, patients with pleocytosis had a higher ARR (0.60 ± 0.09 vs 0.48 ± 0.04; = 0.0267) and a steeper increase (slope) in the EDSS score throughout the follow-up period (correlation coefficient: r = 0.04; = 0.0251).
CSF pleocytosis may be considered a biological unfavorable predictive factor regarding disease course and progression in MS.
多发性硬化症(MS)是一种脱髓鞘的中枢神经系统疾病,其病程和预后存在多种临床表型。尽管在对患者进行初始评估时考虑了多种预后因素,但目前仍缺乏能定义疾病病程并指导治疗的生物学标志物。脑脊液中细胞增多的患者与脑脊液中细胞无增多的患者在症状、病程和预后方面是否存在差异尚不清楚。本研究旨在评估初诊时脑脊液中细胞增多是否对 MS 的临床病程和进展有影响。
我们回顾性评估了 1999 年 1 月至 2016 年 1 月期间在拉宾医学中心多发性硬化症门诊就诊并在发病时进行了腰椎穿刺(LP)的患者,考虑了脑脊液细胞计数、临床诊断(孤立综合征[CIS]和复发缓解型多发性硬化症[RRMS])、年复发率(ARR)、临床前发现(影像学、脑脊液寡克隆带和诱发电位)以及疾病进展,以扩展残疾状况量表(EDSS)表示。
共有 114 名患者(72 名女性)在发病时进行了 LP(RRMS:n = 100,CIS:n = 14)。诊断时的年龄为 32.4 ± 12.2 岁,随访时间为 9.4 ± 3.8 年。46 名患者的脑脊液中细胞增多(≥5 个/μL)。与脑脊液细胞计数<4 个/μL 的患者相比,细胞增多的患者 ARR 更高(0.60 ± 0.09 比 0.48 ± 0.04;P=0.0267),整个随访期间 EDSS 评分的增加幅度更大(斜率)(相关系数:r = 0.04;P=0.0251)。
脑脊液中细胞增多可能被视为 MS 病程和进展方面的生物学不良预后因素。