Neurology Unit, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.
Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Eur J Neurol. 2022 Feb;29(2):564-572. doi: 10.1111/ene.15161. Epub 2021 Nov 9.
This study was undertaken to assess the long-term outcome of patients with paraneoplastic and non paraneoplastic autoimmune cerebellar ataxia (ACA) using the Scale for the Assessment and Rating of Ataxia (SARA).
Patients with subacute cerebellar ataxia admitted to our institution between September 2012 and April 2020 were prospectively recruited. Serum and/or cerebrospinal fluid was tested for neural autoantibodies by indirect immunofluorescence on mouse brain, cell-based assays, and radioimmunoassay. SARA and modified Rankin Scale (mRS) score were employed to assess patients' outcome.
Fifty-five patients were recruited, of whom 23 (42%) met the criteria for cerebellar ataxia of autoimmune etiology. Neural autoantibodies were detected in 22 of 23 patients (Yo-immunoglobulin G [IgG], n = 6; glutamic acid decarboxylase 65-IgG, n = 3; metabotropic glutamate receptor 1-IgG, n = 2; voltage-gated calcium channel P/Q type-IgG, n = 2; Hu-IgG, n = 1; glial fibrillary acidic protein-IgG, n = 1; IgG-binding unclassified antigens, n = 7). Thirteen patients were diagnosed with paraneoplastic cerebellar syndrome (PCS) and 10 with idiopathic ACA. All patients received immunotherapy. Median SARA score was higher in the PCS group at all time points (p = 0.0002), while it decreased significantly within the ACA group (p = 0.049) after immunotherapy. Patients with good outcome (mRS ≤ 2) had less neurological disability (SARA < 15) at disease nadir (p = 0.039) and presented less frequently with paraneoplastic neurological syndrome (p = 0.0028). The univariate linear regression model revealed a good correlation between mRS and SARA score both at disease onset (p < 0.0001) and at last follow-up (p < 0.0001). SARA score < 11 identified patients with good outcome.
Patients with idiopathic ACA significantly improved after immunotherapy. SARA score accurately reflects patients' clinical status and may be a suitable outcome measure for patients with ACA.
本研究旨在使用共济失调评估和评定量表(SARA)评估副肿瘤和非副肿瘤自身免疫性小脑性共济失调(ACA)患者的长期预后。
2012 年 9 月至 2020 年 4 月期间,我们机构连续前瞻性招募了患有亚急性小脑共济失调的患者。通过间接免疫荧光法在鼠脑、细胞基础测定和放射免疫测定上检测血清和/或脑脊液中的神经自身抗体。采用 SARA 和改良 Rankin 量表(mRS)评分评估患者的预后。
共招募了 55 名患者,其中 23 名(42%)符合自身免疫性病因小脑共济失调的标准。在 23 名患者中检测到神经自身抗体 22 例(Yo-免疫球蛋白 G [IgG],n = 6;谷氨酸脱羧酶 65-IgG,n = 3;代谢型谷氨酸受体 1-IgG,n = 2;电压门控钙通道 P/Q 型-IgG,n = 2;Hu-IgG,n = 1;胶质纤维酸性蛋白-IgG,n = 1;IgG 结合未分类抗原,n = 7)。13 名患者诊断为副肿瘤性小脑综合征(PCS),10 名患者诊断为特发性 ACA。所有患者均接受免疫治疗。在所有时间点,PCS 组的中位数 SARA 评分均较高(p = 0.0002),而 ACA 组在免疫治疗后显著降低(p = 0.049)。预后良好(mRS≤2)的患者在疾病高峰时的神经功能缺损程度较低(SARA<15)(p = 0.039),并且较少出现副肿瘤性神经系统综合征(p = 0.0028)。单变量线性回归模型显示,在疾病发病时(p<0.0001)和最后一次随访时(p<0.0001),mRS 与 SARA 评分之间存在良好的相关性。SARA 评分<11 可识别预后良好的患者。
特发性 ACA 患者经免疫治疗后显著改善。SARA 评分准确反映了患者的临床状况,可能是 ACA 患者的一种合适的疗效评价指标。