Anti-glutamic acid decarboxylase antibodies-associated cerebellar ataxia: A treatable ataxia

Q3 Medicine Annals of Movement Disorders Pub Date : 2024-03-21 DOI:10.4103/aomd.aomd_23_23
RohanR Mahale, Sandeep M, Anita Mahadevan, N. Kamble, V. Holla, R. Mundlamuri, S. Vengalil, N. M, A. Nalini, P. Pal, Ravi Yadav
{"title":"Anti-glutamic acid decarboxylase antibodies-associated cerebellar ataxia: A treatable ataxia","authors":"RohanR Mahale, Sandeep M, Anita Mahadevan, N. Kamble, V. Holla, R. Mundlamuri, S. Vengalil, N. M, A. Nalini, P. Pal, Ravi Yadav","doi":"10.4103/aomd.aomd_23_23","DOIUrl":null,"url":null,"abstract":"\n \n \n 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.\n \n \n \n To study the clinical, radiological profile, associated neoplasm, treatment outcome, and prognosis in patients diagnosed with anti-GAD65Ab-associated CA.\n \n \n \n A retrospective descriptive analysis of a cohort of patients diagnosed with anti-GAD65Ab-associated CA was performed and analyzed.\n \n \n \n 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.\n \n \n \n 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.\n","PeriodicalId":7973,"journal":{"name":"Annals of Movement Disorders","volume":"26 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Movement Disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/aomd.aomd_23_23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
Annals of Movement Disorders
Annals of Movement Disorders Medicine-Surgery
CiteScore
0.60
自引率
0.00%
发文量
0
审稿时长
17 weeks
期刊最新文献
Subacute sclerosing panencephalitis presenting as repeated extension of the neck: A case report Mitochondrial membrane protein-associated neurodegeneration presenting with pure motor neuropathy: A rare case report and review of the literature SCA 15 presenting with parkinsonism–dystonia, tremor, and psychosis in an Indian woman The impact of bilateral subthalamic nucleus deep brain stimulation on dyskinesia and levodopa equivalent daily dose in advanced Parkinson’s disease An interesting case of ocular flutter, myoclonus, and ataxia in the postpartum period
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1