抗谷氨酸脱羧酶抗体相关性小脑共济失调:可治疗的共济失调

Q3 Medicine
RohanR Mahale, Sandeep M, Anita Mahadevan, N. Kamble, V. Holla, R. Mundlamuri, S. Vengalil, N. M, A. Nalini, P. Pal, Ravi Yadav
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引用次数: 0

摘要

抗谷氨酸脱羧酶65抗体相关性小脑共济失调(anti-GAD65Ab-associated CA)是研究最为广泛的免疫介导型共济失调。评估抗GAD65Ab相关性小脑共济失调的临床、放射学、治疗概况和预后的病例系列很少。 研究确诊为抗 GAD65Ab 相关 CA 患者的临床、放射学特征、相关肿瘤、治疗效果和预后。 对一组确诊为抗 GAD65Ab 相关 CA 的患者进行回顾性描述性分析。 13名患者被选中进行分析,其中女性占多数(70%)。患者发病时的平均年龄为 47.5 ± 11.1 岁(29-65 岁),症状持续时间的中位数为 4 个月。所有13名患者(100%)均有步态共济失调。10名患者在步态共济失调的同时还伴有肢体共济失调(75%)。七名患者有小脑构音障碍(54%)。四名患者(31%)有凝视诱发的眼球震颤。五名患者(39%)被诊断出患有2型糖尿病,一名患者在患有2型糖尿病的同时还患有甲状腺功能减退症。七名患者(54%)的脑磁共振成像正常,六名患者出现单纯性小脑萎缩。一名患者被查出患有结肠肿瘤。所有 13 名患者均接受了静脉甲基强的松龙治疗,随后又口服了 3 个月的类固醇。六名患者(50%)在静脉注射甲基强的松龙的同时接受了血浆置换。五名患者的治疗效果良好(改良兰金量表评分≤2),两名患者的治疗效果不佳;六名患者在首次入院后失去了随访机会。 抗GAD65Ab相关的CA表现为亚急性至慢性进展性CA,免疫治疗效果良好。对于亚急性至慢性散发性CA患者,应评估血清或脑脊液中的抗GAD抗体。抗GAD65Ab相关CA很少发生系统性肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-glutamic acid decarboxylase antibodies-associated cerebellar ataxia: A treatable ataxia
Anti-glutamate decarboxylase 65 antibody-associated cerebellar ataxia (anti-GAD65Ab-associated CA) is the most widely studied immune-mediated CA. There are few case series evaluating the clinical, radiological, treatment profile, and outcome of anti-GAD65Ab-associated CA. To study the clinical, radiological profile, associated neoplasm, treatment outcome, and prognosis in patients diagnosed with anti-GAD65Ab-associated CA. A retrospective descriptive analysis of a cohort of patients diagnosed with anti-GAD65Ab-associated CA was performed and analyzed. Thirteen patients were selected for the analysis with female predominance (70%). The mean age at presentation was 47.5 ± 11.1 years (range, 29–65 years), and the median duration of the symptoms was 4 months. All 13 patients (100%) had gait ataxia. Ten patients had limb ataxia along with gait ataxia (75%). Seven patients had cerebellar dysarthria (54%). Four patients (31%) had gaze-evoked jerky nystagmus. Five patients (39%) were diagnosed with type 2 diabetes mellitus, and one patient had hypothyroidism in addition to type 2 diabetes mellitus. Brain magnetic resonance imaging was normal in seven (54%) patients, and pure cerebellar atrophy was observed in six patients. One patient was detected with a colon neoplasm. All 13 patients received intravenous methylprednisolone, followed by oral steroids over 3 months. Six patients (50%) received plasma exchange along with intravenous methylprednisolone. Favorable outcomes (modified Rankin scale score ≤2) were observed in five patients and poor outcomes in two; six patients were lost to follow-up after the first admission. Anti-GAD65Ab-associated CA presents as subacute to chronic progressive CA with a favorable outcome with immunotherapy. Anti-GAD antibodies should be assessed in serum or cerebrospinal fluid in patients presenting subacute to chronic sporadic CA. The occurrence of a systemic neoplasm is rare in anti-GAD65Ab-associated CA.
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来源期刊
Annals of Movement Disorders
Annals of Movement Disorders Medicine-Surgery
CiteScore
0.60
自引率
0.00%
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审稿时长
17 weeks
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