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伴或不伴先兆的家族性偏头痛:临床特征及共病情况

Familial migraine with and without aura: clinical characteristics and co-occurrence.

作者信息

Kallela M, Wessman M, Havanka H, Palotie A, Färkkilä M

机构信息

Department of Neurology, University of Helsinki Central Hospital, Haartmaninkatu 4, 00290 Helsinki, Finland.

出版信息

Eur J Neurol. 2001 Sep;8(5):441-9. doi: 10.1046/j.1468-1331.2001.00260.x.

Abstract

Migraine with aura (MwA) and migraine without aura (MwoA) are the two common forms of migraine. Many migraine patients suffer from both kinds of attacks. In a questionnaire-based study using the current International Headache Society (IHS) criteria we determined the clinical characteristics and occurrence of MwA + MwoA in 1000 migraine patients belonging to 210 Finnish migraine families. Nine hundred and six patients were able to indicate whether they suffered from MwA (but not MwoA), migraine aura without headache (migraine equivalent) (but not MwA) or MwA and MwoA. Of these patients, 3.2% had experienced MwoA, 11.1% MwA, 40.6% MwA + MwoA, 23.5% MwoA and 20.3% MwA-like symptoms not meeting the IHS criteria. The high prevalence of MwA attacks in the families studied supports the belief that aura has a strong hereditary component. The MwA + MwoA patients had significantly more severe attacks, more typical headache and more prodromal symptoms than the MwA and MwoA subjects. Therefore, it is possible that there is a continuum with pure MwA at the neural and pure MwoA at the headache end of the spectrum, and MwA + MwoA lying in between the two. The MwA + MwoA patients would thus be liable to both types of migraine, making their attacks more characteristic and more severe. This would also explain why the co-occurrence of MwA and MwoA is more common in the clinic compared with population based epidemiological studies. These findings have consequences for future research on liability genes for migraine.

摘要

伴先兆偏头痛(MwA)和无先兆偏头痛(MwoA)是偏头痛的两种常见形式。许多偏头痛患者这两种发作类型都会经历。在一项基于问卷调查且采用当前国际头痛协会(IHS)标准的研究中,我们确定了来自210个芬兰偏头痛家族的1000名偏头痛患者中MwA + MwoA的临床特征及发生率。906名患者能够指出他们是否患有MwA(但无MwoA)、无头痛的偏头痛先兆(偏头痛等效症)(但无MwA)或MwA和MwoA。在这些患者中,3.2%经历过MwoA,11.1%经历过MwA,40.6%经历过MwA + MwoA,23.5%经历过MwoA,20.3%有不符合IHS标准的类似MwA的症状。在研究的家族中MwA发作的高患病率支持了先兆具有很强遗传成分这一观点。与MwA和MwoA患者相比,MwA + MwoA患者的发作明显更严重,头痛更典型,前驱症状更多。因此,有可能在频谱的神经端存在纯MwA与头痛端的纯MwoA之间的连续体,而MwA + MwoA处于两者之间。MwA + MwoA患者因此易患两种类型的偏头痛,使其发作更具特征性且更严重。这也可以解释为什么在临床中MwA和MwoA的共现比基于人群的流行病学研究中更常见。这些发现对未来偏头痛易患基因的研究有影响。

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