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偏头痛与神经遗传障碍。

Migraine and neurogenetic disorders.

机构信息

Saint Joseph's Regional Medical Center, 703 Main Street, X618, Paterson, NJ 07503, USA.

出版信息

Curr Pain Headache Rep. 2013 Sep;17(9):360. doi: 10.1007/s11916-013-0360-9.

DOI:10.1007/s11916-013-0360-9
PMID:23904204
Abstract

In the current classification of headache disorders, headache attributable to genetic disorders is not classified separately, rather as headache attributed to cranial or cervical vascular disorder. The classification thus implies that a vascular pathology causes headache in these genetic disorders. Unquestionably, migraine is one of the prominent presenting features of several genetic cerebral small vessel diseases such as cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy, retinal vasculopathy with cerebral leukodystrophy, and hereditary infantile hemiparessis, retinal arteriolar tortuosity and leukoencephalopahty. Shared genetic features, increased susceptibility, and/or vascular endothelial dysfunction may play a role in pathogenesis of migraine. Common or overlapping pathways involving the responsible genes may provide insight regarding the pathophysiological mechanisms that can explain their comorbidity with migraine. This review focuses on clinical features of genetic vasculopathies. An independent category-migraine related to genetic disorders-should be considered to classify these disorders.

摘要

在当前的头痛障碍分类中,归因于遗传疾病的头痛并未单独分类,而是归类为归因于颅或颈血管障碍的头痛。因此,该分类意味着血管病理学在这些遗传疾病中引起头痛。毫无疑问,偏头痛是几种遗传性脑小血管疾病的突出表现之一,例如伴有皮质下梗死和白质脑病的脑常染色体显性动脉病、伴有脑白质营养不良的视网膜血管病变、遗传性婴儿偏瘫、视网膜小动脉迂曲和白质脑病。遗传特征、易感性增加和/或血管内皮功能障碍可能在偏头痛发病机制中起作用。涉及相关基因的常见或重叠途径可能有助于了解可以解释其与偏头痛并存的病理生理机制。这篇综述重点介绍了遗传血管病的临床特征。应该考虑将与遗传障碍相关的偏头痛作为一个独立的类别来对这些障碍进行分类。

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Migraine and neurogenetic disorders.偏头痛与神经遗传障碍。
Curr Pain Headache Rep. 2013 Sep;17(9):360. doi: 10.1007/s11916-013-0360-9.
2
Migraine and genetic and acquired vasculopathies.偏头痛与遗传性及后天性血管病变
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Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy.遗传性婴儿偏瘫、视网膜小动脉迂曲和白质脑病。
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本文引用的文献

1
Acetazolamide for the prophylaxis of migraine in CADASIL: a preliminary experience.乙酰唑胺预防 CADASIL 偏头痛:初步经验。
J Headache Pain. 2012 Jun;13(4):299-302. doi: 10.1007/s10194-012-0426-9. Epub 2012 Feb 25.
2
Simultaneous impairment of intracranial and peripheral artery vasoreactivity in CADASIL patients.CADASIL 患者颅内和外周动脉血管反应性同时受损。
Cerebrovasc Dis. 2012;33(2):128-34. doi: 10.1159/000334185. Epub 2011 Dec 14.
3
Cortical folding influences migraine aura symptoms in CADASIL.皮质折叠影响 CADASIL 偏头痛先兆症状。
J Neurol Neurosurg Psychiatry. 2012 Feb;83(2):213-6. doi: 10.1136/jnnp-2011-300825. Epub 2011 Nov 9.
4
Impaired vasoreactivity in mildly disabled CADASIL patients.CADASIL 轻度残疾患者的血管反应受损。
J Neurol Neurosurg Psychiatry. 2012 Mar;83(3):268-74. doi: 10.1136/jnnp-2011-300080. Epub 2011 Nov 9.
5
Assessment of cerebral hemodynamics to acetazolamide using brain perfusion SPECT in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.使用脑灌注 SPECT 评估脑型常染色体显性遗传性脑动脉病伴皮质下梗死和白质脑病中的乙酰唑胺脑血流动力学。
Clin Nucl Med. 2011 Feb;36(2):158-9. doi: 10.1097/RLU.0b013e3182073c0f.
6
Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature.CADASIL 的发病机制:转染和基因敲除小鼠探索突变基因 Notch3 在脑血管中的功能和失能。
Bioessays. 2011 Jan;33(1):73-80. doi: 10.1002/bies.201000093. Epub 2010 Oct 21.
7
Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges.脑小血管病:从发病机制和临床特征到治疗挑战。
Lancet Neurol. 2010 Jul;9(7):689-701. doi: 10.1016/S1474-4422(10)70104-6.
8
Acetazolamide improves cerebral hemodynamics in CADASIL.乙酰唑胺可改善 CADASIL 患者的脑血流动力学。
J Neurol Sci. 2010 May 15;292(1-2):77-80. doi: 10.1016/j.jns.2010.01.023. Epub 2010 Mar 12.
9
Acute headache followed by focal neuropsychological impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).脑常染色体显性动脉病伴皮质下梗死和白质脑病(CADASIL)患者出现急性头痛,随后出现局灶性神经认知功能障碍。
J Stroke Cerebrovasc Dis. 2010 Jan;19(1):75-6. doi: 10.1016/j.jstrokecerebrovasdis.2009.03.001.
10
Migraine and genetic and acquired vasculopathies.偏头痛与遗传性及后天性血管病变
Cephalalgia. 2009 Sep;29(9):1006-17. doi: 10.1111/j.1468-2982.2009.01940.x.