Clinical epidemiology and analysis of pathomechanisms of optic-spinal form of multiple sclerosis

视脊髓型多发性硬化症的临床流行病学及发病机制分析

基本信息

  • 批准号:
    09470150
  • 负责人:
  • 金额:
    $ 2.56万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    1997
  • 资助国家:
    日本
  • 起止时间:
    1997 至 1998
  • 项目状态:
    已结题

项目摘要

We studied clinical features and pathomechanisms of multiple sclerosis (MS) in Japan, especially optic-spinal form of MS (OSMS). (l)Eighty six cases of MS whose onset of disease were during 1970-1998 were clinically classified. Frequency of cases of MS with acute transverse myelitis (ATM) decreased in 1980s and 1990s compared with 1970s. In contrast, OSMS without ATM and conventinal MS increased in 1 980s. Changes of environmental factors might have caused these changes of clinical picture of MS in Japan. Brainstem and cerebellar symptoms and signs and MRI findings were analyzed in 66 consecutive cases of MS, and 65% had those symptoms and signs. Cerebellarsigns were seen in 30%. Moreover, cerebellar lesions on MRI were seen in only 6.4%, which was significantly lower than the figures in Western countries (50-90%). (2)4-aminopyridine (4-AP) relieves conductionlock in demyelinated nerves by blocking K channels. 4-AP was administered intravenously and motor evoked potentials (MEP) were recorded before and after 4-AP therapy. After 4-AP therapy, MEP amplitudes increased significantly and mean consecutive difference of MEP latency decreased significantly. 4-AP probably caused coordinated contraction of more muscle fibers. (3) Parvovirus 819 (B19) infection is associated with autoimmunity. B19 antibodies in sera and cerebrospinal fluid (CSF) and B19 DNA in CSF were studied in 46 MS patients. Frequency of B19 lgG in MS (65%) was significantly higher than that in controls (40%), but serum 819 lgM and B19 DNA in CSF were consistently negative in excerbation of MS.
我们研究了日本多发性硬化症(MS)的临床特征和病理机制,特别是光学脊髓型多发性硬化症(OSMS)。(1)对发病时间为1970 ~ 1998年的86例多发性硬化症进行临床分类。与20世纪70年代相比,20世纪80年代和90年代MS合并急性横贯脊髓炎(ATM)的发病率有所下降。相比之下,无ATM的OSMS和常规MS在20世纪80年代有所增加。环境因素的变化可能是造成日本多发性硬化症临床表现变化的原因。对66例MS患者的脑干和小脑症状、体征及MRI表现进行分析,65%的患者存在上述症状和体征。30%可见小脑征象。此外,MRI上小脑病变的发生率仅为6.4%,明显低于西方国家(50-90%)。(2)4-氨基吡啶(4-AP)通过阻断K通道缓解脱髓鞘神经的传导锁定。静脉给予4-AP治疗,记录4-AP治疗前后的运动诱发电位(MEP)。经4-AP治疗后,MEP振幅显著升高,MEP潜伏期平均连续差显著减小。4-AP可能引起更多肌肉纤维的协调收缩。细小病毒819 (B19)感染与自身免疫有关。对46例MS患者血清、脑脊液B19抗体及脑脊液B19 DNA进行了检测。MS患者血清B19 lgM和脑脊液B19 DNA的检出率(65%)明显高于对照组(40%),但MS患者血清819 lgM和脑脊液B19 DNA均呈阴性。

项目成果

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专利数量(0)
Fujihara K.: "The effects of 4-aminopvridine on motor evoked potentials in multiple sclerosis" J Neurol Sci.vol 159. 102-106 (1998)
Fujihara K.:“4-氨基吡啶对多发性硬化症运动诱发电位的影响”J Neurol Sci.vol 159. 102-106 (1998)
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    0
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  • 通讯作者:
糸山泰人: "多発性硬化症の病因と病態" 日本内科学会雑誌. 87・4. 604-611 (1998)
Yasuto Itoyama:“多发性硬化症的病因学和病理学”日本内科医学会杂志87・4(1998)。
  • DOI:
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    0
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  • 通讯作者:
Nakashima I: "Human parvovirus B19 infection in multiple sclerosis" European Neurology. in press.
Nakashima I:“多发性硬化症中的人类细小病毒 B19 感染”欧洲神经病学。
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    0
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Nakashima I.: "Clinical and laboratory features of myelitis patients with anti-neutrophi cytoplasmic antibodies." J Neurol Sci.vol.157. 60-66 (1998)
Nakashima I.:“具有抗中性粒细胞胞浆抗体的脊髓炎患者的临床和实验室特征。”
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  • 影响因子:
    0
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Shiga Y: "Complement activation as a cause of transient hypotension during plasmapheresis" Artif Organs. 22・12. 1067-1069 (1998)
Shiga Y:“补体激活是血浆置换过程中短暂性低血压的原因”Artif Organs 22・1069(1998)。
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ITOYAMA Yasuto其他文献

ITOYAMA Yasuto的其他文献

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{{ truncateString('ITOYAMA Yasuto', 18)}}的其他基金

Establishment of a new disease entity as astrocytopathy, and studies on the pathogenesis and treatment for neuromyelitis optica
星形细胞病新病种的建立及视神经脊髓炎的发病机制和治疗研究
  • 批准号:
    22229008
  • 财政年份:
    2010
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Scientific Research (S)
Elucidate the pathomechanism of inclusion body myositis(IBM)
阐明包涵体肌炎(IBM)的发病机制
  • 批准号:
    22659167
  • 财政年份:
    2010
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Optic-spinal multiple sclerosis : clarification of pathogenesis, establishment of new disease entity and treatment
视脊髓多发性硬化症:发病机制的阐明、新疾病实体的建立和治疗
  • 批准号:
    19209032
  • 财政年份:
    2007
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
A Study on the Pathogenesis and Therapy of Optic-Spinal Multiple Sclerosis
视神经脊髓多发性硬化症的发病机制及治疗研究
  • 批准号:
    17390250
  • 财政年份:
    2005
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
COMPARATIVE ANALYSIS OF CLINICAL AND MOLECULAR IMMUNOLOGICAL PATHOGENESES IN SUBTYPES OF MULTIPLE SCLEROSIS IN JAPAN
日本多发性硬化症亚型临床及分子免疫病因比较分析
  • 批准号:
    15390271
  • 财政年份:
    2003
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Comparative analysis of molecular immunopathogenesis in optic-spinal and conventional multiple sclerosis
视神经脊髓病与传统多发性硬化症分子免疫发病机制的比较分析
  • 批准号:
    13470131
  • 财政年份:
    2001
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Mutational analysis in dysferlin gene in patients with muscular dystrophy in Japanese populations.
日本人群肌营养不良症患者 Dysferlin 基因突变分析。
  • 批准号:
    12557058
  • 财政年份:
    2000
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Genetic analysis in families with amyotrophic lateral sclerosis
肌萎缩侧索硬化症家族的遗传分析
  • 批准号:
    11470144
  • 财政年份:
    1999
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B).
Molecular genetic study of familial ALS in Japan
日本家族性 ALS 的分子遗传学研究
  • 批准号:
    07457152
  • 财政年份:
    1995
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Study of Immunomechanisms in HTLV-I-Associated Myelopathy(HAM)
HTLV-I相关性脊髓病(HAM)的免疫机制研究
  • 批准号:
    63480217
  • 财政年份:
    1988
  • 资助金额:
    $ 2.56万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)

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Programmable Hydrogels for Optimized Human Oligodendrocyte Transplantation in Demyelinating Disease
用于优化人类少突胶质细胞移植治疗脱髓鞘疾病的可编程水凝胶
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    2022
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Effector-Regulator Immune Interactions During Autoimmune Demyelinating Disease
自身免疫性脱髓鞘疾病期间效应器-调节器免疫相互作用
  • 批准号:
    10359998
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    2022
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    $ 2.56万
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How do synaptic connections change in demyelinating disease?
脱髓鞘疾病中突触连接如何变化?
  • 批准号:
    10210166
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    2021
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How Do Synaptic Connections Change in Demyelinating Disease?
脱髓鞘疾病中突触连接如何变化?
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脱髓鞘疾病中突触连接如何变化?
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中枢神经系统脱髓鞘疾病的神经元抗原监测和自身免疫
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    10380683
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    2020
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Neuronal antigen surveillance and autoimmunity in CNS demyelinating disease
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  • 批准号:
    10213156
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中枢神经系统脱髓鞘疾病的神经元抗原监测和自身免疫
  • 批准号:
    10609862
  • 财政年份:
    2020
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    $ 2.56万
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Neuronal antigen surveillance and autoimmunity in CNS demyelinating disease
中枢神经系统脱髓鞘疾病的神经元抗原监测和自身免疫
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    10063399
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