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偏头痛:一种遗传性疾病?

Migraine: a genetic disease?

作者信息

Montagna Pasquale

机构信息

Department of Neurological Sciences, University of Bologna Medical School, Via U. Foscolo 7, 40123 Bologna, Italy.

出版信息

Neurol Sci. 2008 May;29 Suppl 1:S47-51. doi: 10.1007/s10072-008-0886-5.

DOI:10.1007/s10072-008-0886-5
PMID:18545896
Abstract

Migraines carry a substantial genetic liability, and in families affected with the typical migraines (migraine with, MA, and without aura, MO) linkage to some chromosomal loci has been reported. As yet however, no genes are known for MA/MO, while the three genes discovered as responsible for familial hemiplegic migraine (FHM) are not involved in the typical migraines. Accordingly, we propose to consider FHM as a syndromic migraine and not as a variety of MA. Moreover, we suggest that epigenetic mechanisms play a role in the determination of the typical migraines, and that the primary headaches represent behavioural responses (sickness behaviour, fight-or-flight responses), having adaptive advantage and having been evolutionary conserved, in which pain represents a signal of homeostatic imbalance. Epigenetic mechanisms and this proposed genetic behavioural model could be usefully incorporated into headache genetic research.

摘要

偏头痛具有显著的遗传易感性,在患有典型偏头痛(伴有先兆偏头痛,MA,和无先兆偏头痛,MO)的家族中,已报道了与某些染色体位点的连锁关系。然而,目前尚未发现与MA/MO相关的基因,而发现的三个导致家族性偏瘫性偏头痛(FHM)的基因并不参与典型偏头痛的发病。因此,我们建议将FHM视为一种综合征性偏头痛,而非MA的一种类型。此外,我们认为表观遗传机制在典型偏头痛的发生中起作用,并且原发性头痛代表行为反应(疾病行为、战斗或逃跑反应),具有适应性优势且在进化过程中得以保留,其中疼痛代表内稳态失衡的信号。表观遗传机制和这种提出的遗传行为模型可有效地纳入头痛遗传学研究。

相似文献

1
Migraine: a genetic disease?偏头痛:一种遗传性疾病?
Neurol Sci. 2008 May;29 Suppl 1:S47-51. doi: 10.1007/s10072-008-0886-5.
2
Migraine genetics.偏头痛遗传学
Expert Rev Neurother. 2008 Sep;8(9):1321-30. doi: 10.1586/14737175.8.9.1321.
3
The physiopathology of migraine: the contribution of genetics.偏头痛的生理病理学:遗传学的作用。
Neurol Sci. 2004 Oct;25 Suppl 3:S93-6. doi: 10.1007/s10072-004-0261-0.
4
The primary headaches: genetics, epigenetics and a behavioural genetic model.原发性头痛:遗传学、表观遗传学及行为遗传模型
J Headache Pain. 2008 Apr;9(2):57-69. doi: 10.1007/s10194-008-0026-x. Epub 2008 Mar 15.
5
Coexisting typical migraine in familial hemiplegic migraine.家族性偏瘫型偏头痛中伴发典型偏头痛。
Neurology. 2010 Feb 16;74(7):594-600. doi: 10.1212/WNL.0b013e3181cff79d.
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The inheritance of migraine with aura estimated by means of structural equation modelling.通过结构方程模型估计伴先兆偏头痛的遗传方式。
J Med Genet. 1999 Mar;36(3):225-7.
7
[Genetic aspects of migraine].[偏头痛的遗传学方面]
Tidsskr Nor Laegeforen. 2003 Oct 9;123(19):2727-30.
8
Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.常见偏头痛形式聚集的家族中ATP1A2基因的罕见错义变异。
Hum Mutat. 2005 Oct;26(4):315-21. doi: 10.1002/humu.20229.
9
Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility.将CACNA1A基因作为典型偏头痛易感性候选基因的研究。
Am J Med Genet. 2001 Dec 8;105(8):707-12. doi: 10.1002/ajmg.1609.
10
[An update on the familial headache syndromes].[家族性头痛综合征的最新进展]
Rinsho Shinkeigaku. 2004 Nov;44(11):944-7.

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Pharmacoinformatics elucidation of potential drug targets against migraine to target ion channel protein KCNK18.药物信息学阐明针对偏头痛的潜在药物靶点以作用于离子通道蛋白KCNK18。
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Curr Genomics. 2013 Aug;14(5):300-15. doi: 10.2174/13892029113149990007.
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Interaction between γ-aminobutyric acid A receptor genes: new evidence in migraine susceptibility.γ-氨基丁酸 A 受体基因相互作用:偏头痛易感性的新证据。
PLoS One. 2013 Sep 5;8(9):e74087. doi: 10.1371/journal.pone.0074087. eCollection 2013.
7
Serum levels of N-acetyl-aspartate in migraine and tension-type headache.偏头痛和紧张型头痛患者血清 N-乙酰天冬氨酸水平。
J Headache Pain. 2012 Jul;13(5):389-94. doi: 10.1007/s10194-012-0448-3. Epub 2012 Apr 17.
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Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?SCN1A 基因多态性与儿童和青少年原发性头痛及特发性或隐源性癫痫:是否存在关联?
J Headache Pain. 2011 Aug;12(4):435-41. doi: 10.1007/s10194-011-0359-8. Epub 2011 Jun 29.