• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

多发性硬化症患者大脑的再髓鞘化能力会随着疾病慢性化而下降。

Remyelination capacity of the MS brain decreases with disease chronicity.

作者信息

Goldschmidt T, Antel J, König F B, Brück W, Kuhlmann T

机构信息

Department of Neuropathology, University Medical Center, Göttingen, Germany.

出版信息

Neurology. 2009 Jun 2;72(22):1914-21. doi: 10.1212/WNL.0b013e3181a8260a.

DOI:10.1212/WNL.0b013e3181a8260a
PMID:19487649
Abstract

OBJECTIVE

To analyze and compare the extent of remyelination in lesions from patients with multiple sclerosis (MS) who have a short (early MS lesions) or a long (chronic MS lesions) disease duration and to determine the influence of anatomic localization on the extent of remyelination. In early MS lesions, remyelination has been described as a relatively frequent event, in contrast to chronic MS lesions, where remyelination is absent or limited to the lesion border in the majority of lesions. However, no studies have been published that have quantified and compared the extent of remyelination in early and chronic MS lesions.

METHODS

We analyzed the occurrence of remyelination in 52 biopsies from 51 patients (early MS) and in 174 lesions from 36 autopsy cases (chronic MS) by immunohistochemistry for myelin proteins, and correlated our findings with anatomic localization, sex, age, and disease duration.

RESULTS

Significantly more lesions were remyelinated in early than in chronic MS (80.7% vs 60%). In chronic MS, subcortical lesions showed more extensive remyelination than periventricular lesions. The majority of cerebellar lesions were completely demyelinated.

CONCLUSION

In summary, our data demonstrate that remyelination is a frequent event in early multiple sclerosis lesions. Furthermore, the anatomic localization of a lesion might influence the extent of remyelination.

摘要

目的

分析和比较疾病病程较短(早期多发性硬化症病变)或较长(慢性多发性硬化症病变)的多发性硬化症(MS)患者病变中的髓鞘再生程度,并确定解剖定位对髓鞘再生程度的影响。在早期MS病变中,髓鞘再生被描述为相对常见的事件,而在慢性MS病变中,大多数病变的髓鞘再生不存在或仅限于病变边界。然而,尚未发表过量化和比较早期和慢性MS病变中髓鞘再生程度的研究。

方法

我们通过对髓鞘蛋白进行免疫组织化学分析,研究了51例患者的52份活检标本(早期MS)和36例尸检病例的174个病变(慢性MS)中的髓鞘再生情况,并将我们的研究结果与解剖定位、性别、年龄和病程进行了关联分析。

结果

早期MS中髓鞘再生的病变明显多于慢性MS(80.7%对vs 60%)。在慢性MS中,皮质下病变的髓鞘再生比脑室周围病变更广泛。大多数小脑病变完全脱髓鞘。

结论

总之,我们的数据表明,髓鞘再生在早期多发性硬化症病变中是常见事件。此外,病变的解剖定位可能会影响髓鞘再生的程度。

相似文献

1
Remyelination capacity of the MS brain decreases with disease chronicity.多发性硬化症患者大脑的再髓鞘化能力会随着疾病慢性化而下降。
Neurology. 2009 Jun 2;72(22):1914-21. doi: 10.1212/WNL.0b013e3181a8260a.
2
Remyelination is extensive in a subset of multiple sclerosis patients.在一部分多发性硬化症患者中,髓鞘再生广泛存在。
Brain. 2006 Dec;129(Pt 12):3165-72. doi: 10.1093/brain/awl217. Epub 2006 Aug 18.
3
Remyelination can be extensive in multiple sclerosis despite a long disease course.尽管病程漫长,但多发性硬化症中的髓鞘再生仍可能广泛存在。
Neuropathol Appl Neurobiol. 2007 Jun;33(3):277-87. doi: 10.1111/j.1365-2990.2007.00805.x. Epub 2007 Apr 18.
4
Diffusely abnormal white matter in chronic multiple sclerosis: imaging and histopathologic analysis.慢性多发性硬化症中弥漫性异常白质:影像学与组织病理学分析
Arch Neurol. 2009 May;66(5):601-9. doi: 10.1001/archneurol.2009.57.
5
Magnetization transfer ratio evolution with demyelination and remyelination in multiple sclerosis lesions.多发性硬化症病灶中脱髓鞘和再髓鞘化过程中的磁化传递率演变
Ann Neurol. 2008 Feb;63(2):254-62. doi: 10.1002/ana.21302.
6
Homogeneity of active demyelinating lesions in established multiple sclerosis.已确诊多发性硬化症中活动性脱髓鞘病变的同质性
Ann Neurol. 2008 Jan;63(1):16-25. doi: 10.1002/ana.21311.
7
Gender differences in the histopathology of MS?多发性硬化症组织病理学中的性别差异?
J Neurol Sci. 2009 Nov 15;286(1-2):86-91. doi: 10.1016/j.jns.2009.07.014. Epub 2009 Aug 11.
8
Nodal, paranodal and juxtaparanodal axonal proteins during demyelination and remyelination in multiple sclerosis.多发性硬化症脱髓鞘和髓鞘再生过程中的结旁、 paranodal和近结旁轴突蛋白
Brain. 2006 Dec;129(Pt 12):3186-95. doi: 10.1093/brain/awl144. Epub 2006 Jun 9.
9
Sporadic adult-onset leukoencephalopathy with neuroaxonal spheroids mimicking cerebral MS.伴有神经轴突球体的散发性成人起病白质脑病,酷似脑多发性硬化症。
Neurology. 2008 Mar 25;70(13 Pt 2):1128-33. doi: 10.1212/01.wnl.0000304045.99153.8f. Epub 2008 Feb 20.
10
IGF binding protein alterations on periplaque oligodendrocytes in multiple sclerosis: implications for remyelination.多发性硬化症中斑块周围少突胶质细胞上胰岛素样生长因子结合蛋白的改变:对髓鞘再生的影响。
Neurochem Int. 2008 Jun;52(8):1431-5. doi: 10.1016/j.neuint.2008.03.004. Epub 2008 Apr 4.

引用本文的文献

1
Inhomogeneous magnetization transfer (ihMT) imaging reveals variable recovery profiles of active MS lesions according to size and localization.非均匀磁化传递(ihMT)成像显示,活动性多发性硬化症(MS)病灶的恢复情况因大小和位置而异。
Imaging Neurosci (Camb). 2024 Jul 24;2. doi: 10.1162/imag_a_00235. eCollection 2024.
2
Advancing multiple sclerosis management in older adults.推进老年多发性硬化症的管理。
Nat Rev Neurol. 2025 Jul 23. doi: 10.1038/s41582-025-01115-5.
3
Myelin dysfunction in aging and brain disorders: mechanisms and therapeutic opportunities.
衰老与脑部疾病中的髓鞘功能障碍:机制与治疗机遇
Mol Neurodegener. 2025 Jun 15;20(1):69. doi: 10.1186/s13024-025-00861-w.
4
Pathways to Progressive Disability in Multiple Sclerosis: The Role of Glial Cells in Chronic CNS Inflammation.多发性硬化症进展性残疾的途径:神经胶质细胞在慢性中枢神经系统炎症中的作用
Glia. 2025 Oct;73(10):1928-1950. doi: 10.1002/glia.70044. Epub 2025 May 23.
5
Broad rim lesions are a new pathological and imaging biomarker for rapid disease progression in multiple sclerosis.宽边病变是多发性硬化症快速疾病进展的一种新的病理和影像学生物标志物。
Nat Med. 2025 Apr 29. doi: 10.1038/s41591-025-03625-7.
6
Impaired remyelination in late-onset multiple sclerosis.迟发性多发性硬化症中髓鞘再生受损。
Acta Neuropathol. 2025 Apr 1;149(1):30. doi: 10.1007/s00401-025-02868-5.
7
Senescent-like microglia limit remyelination through the senescence associated secretory phenotype.衰老样小胶质细胞通过衰老相关分泌表型限制髓鞘再生。
Nat Commun. 2025 Mar 7;16(1):2283. doi: 10.1038/s41467-025-57632-w.
8
Incomplete remyelination via therapeutically enhanced oligodendrogenesis is sufficient to recover visual cortical function.通过治疗性增强少突胶质细胞生成实现的不完全髓鞘再生足以恢复视觉皮层功能。
Nat Commun. 2025 Jan 16;16(1):732. doi: 10.1038/s41467-025-56092-6.
9
Soma and neurite density abnormalities of paramagnetic rim lesions and core-sign lesions in multiple sclerosis.多发性硬化症中顺磁性边缘病变和核心信号病变的胞体与神经突密度异常
J Neurol. 2025 Jan 15;272(2):145. doi: 10.1007/s00415-025-12887-7.
10
Brain organoid methodologies to explore mechanisms of disease in progressive multiple sclerosis.用于探索进展性多发性硬化症疾病机制的脑类器官方法
Front Cell Neurosci. 2024 Dec 18;18:1488691. doi: 10.3389/fncel.2024.1488691. eCollection 2024.