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脑小血管病白质高信号相关性头晕的发病机制研究进展

Research progress in pathogenesis of white matter hyperintensity related dizziness in small cerebral vascular disease
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摘要 随着神经影像技术的发展,脑小血管病已成为近年来国内外学者的研究热点,已明确其与认知减退、痴呆、步态不稳有关,然而最近研究发现伴有白质高信号的脑小血管病是老年人不明原因慢性头晕的主要病因,但二者相关机制尚不完全清楚,近期研究表明,可能与大脑神经网络离断、视觉依赖、脑组织结构异常引起眼动障碍、氧化应激调节障碍、脑血流自身调节障碍、前庭系统与情绪障碍相互影响等有关。 With the development of neuroimaging technology,cerebral small vessel disease has become a hot research topic in recent years.It has been clearly related to cognitive decline,dementia and gait instability.However,recent studies have found that small cerebral vascular disease with white matter hyperintensities is the main cause of chronic dizziness in the elderly,but the pathogenesis is not completely clear,which may be related to brain neural network disconnection,visual dependence,eye movement disorder caused by abnormal brain tissue structure,oxidative stress regulation disorder,cerebral blood flow self-regulation disorder,and the interaction mechanism between vestibular system and emotional disorder.
作者 吕灿灿 江怡静 卫元晓 方力群 Lyu Cancan;Jiang Yijing;Wei Yuanxiao;Fang Liqun(Department of Neurology,the Fourth Affiliated Hospital of Harbin Medical University,Harbin 150000,China)
出处 《中国综合临床》 2023年第2期147-150,共4页 Clinical Medicine of China
关键词 脑小血管病 白质高信号 头晕 发病机制 Cerebral small vessel disease White matter hyperintensities Dizziness Pathogenesis
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  • 1陈烁,冯娟.脑小血管病变患者脑白质病变程度与步态平衡功能障碍关系分析[J].社区医学杂志,2020,18(21):1471-1474. 被引量:3
  • 2王朝霞,吕鹤,张英,卜定方,牛小媛,张茁,黄一宁,袁云.伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病四个家系的NOTCH3基因突变研究[J].中华医学杂志,2004,84(14):1175-1180. 被引量:10
  • 3Joutel A,Corpechot C,Ducros A,et al.Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL),a mendelian condition causing stroke and vascular dementia[J].Ann N Y Acad Sci,1997,826(1):213-217.
  • 4Liem MK,Lesnik Oberstein SA,Haan J,et al.MRI correlates of cognitive decline in CADASIL:a 7-year follow-up study[J].Neurology,2009,72(2):143-148.
  • 5Herve D,Godin O,Dufouil C,et al.Three-dimensional MRI analysis of individual volume of Lacunes in CADASIL[J].Stroke,2009,40(1):124-128.
  • 6Ishiko A,Shimizu A,Nagata E,et al.Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASIL[J].Acta Neuropathol,2006,112(3):333-339.
  • 7Ishiko A,Shimizu A,Nagata E,et al.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephaloapthy (CADASIL):a hereditary cerebrovascular disease,which can be diagnosed by skin biopsy electron microscopy[J].Am J Dermatopathol,2005,27(2):131-134.
  • 8Liem MK,van der Grond J,Haan J,et al.Lacunar infarcts are the main correlate with cognitive dysfunction in CADASIL[J].Stroke,2007,38(3):923-928.
  • 9Uyguner ZO,Siva A,Kayserili H,et al.The R110C mutation in Notch3 causes variable clinical features in two Turkish families with CADASIL syndrome[J].J Neurol Sci,2006,246(1-2):123-130.
  • 10Dichgans M,Mayer M,Uttner I,et al.The phenotypic spectrum of CADASIL:clinical findings in 102 cases[J].Ann Neurol,1998,44(5):731-739.

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