Department of Neurology, University of L'Aquila, piazzale Salvatore Tommasi 1, 67100 L'Aquila, Italy.
J Headache Pain. 2010 Jun;11(3):181-6. doi: 10.1007/s10194-010-0203-6. Epub 2010 Mar 12.
We reviewed the characteristics of headache in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), to verify the appropriateness of the International Classification of Headache Disorders, second edition (ICHD-II) criteria. Available data were found through Medline/PubMed using the keyword "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)". The search was restricted to studies published in English in the years between 1993 and 2008. We excluded studies that did not report original data on CADASIL and information regarding the presence of headache. We found 34 studies reporting data on 749 patients overall; 387 (51.7%) patients had headache. According to the authors' definition, 356 (92%) patients were reported as having migraine and 31 (8%) as having headache. Of the 356 patients who were defined as migraineurs, 125 (35.1%) had migraine with aura, 7 (2%) migraine without aura, 156 (43.8%) unspecified migraine and 68 (19.1%) had more than one type of migraine. Among the 31 patients reported as suffering from headache, the headache was not further detailed in 18 (58.1%) patients; it was defined as chronic in 6 (19.3%), as resembling migraine with aura in 4 (12.9%), as resembling migraine without aura in 2 (6.5%) and as tension type in 1 (3.2%) patient. In patients with CADASIL, the headache was usually referred to as migraine and mostly as migraine with aura. However, this referral is formally incorrect since the diagnostic criteria for any type of migraine in the ICHD-II require that the disturbance is not attributed to another disorder. For this reason, we suggest updating the ICHD-II in relation to CADASIL. Our suggestion is to insert a new category referred to as Headache attributed to genetic disorder including Headache attributed to CADASIL.
我们回顾了伴有皮质下梗死和白质脑病的脑常染色体显性遗传性动脉病(CADASIL)患者头痛的特征,以验证国际头痛疾病分类,第二版(ICHD-II)标准的适当性。通过 Medline/PubMed 使用关键字“伴有皮质下梗死和白质脑病的脑常染色体显性遗传性动脉病(CADASIL)”查找现有数据。该搜索仅限于 1993 年至 2008 年期间以英文发表的研究。我们排除了未报告 CADASIL 原始数据以及头痛存在信息的研究。我们共发现 34 项研究,涉及 749 例患者;387 例(51.7%)患者存在头痛。根据作者的定义,356 例(92%)患者被报告为偏头痛,31 例(8%)为头痛。在 356 名被定义为偏头痛患者中,125 例(35.1%)有先兆偏头痛,7 例(2%)无先兆偏头痛,156 例(43.8%)为未特指偏头痛,68 例(19.1%)有多种偏头痛。在 31 例报告为头痛的患者中,18 例(58.1%)患者未进一步详细说明头痛;6 例(19.3%)患者将头痛定义为慢性头痛,4 例(12.9%)患者将头痛定义为类似先兆偏头痛,2 例(6.5%)患者将头痛定义为类似无先兆偏头痛,1 例(3.2%)患者将头痛定义为紧张型头痛。在 CADASIL 患者中,头痛通常被称为偏头痛,大多为有先兆偏头痛。然而,这种称谓并不正确,因为 ICHD-II 中任何类型偏头痛的诊断标准都要求该障碍不是归因于其他疾病。出于这个原因,我们建议对 ICHD-II 进行更新,以反映 CADASIL。我们的建议是插入一个新类别,称为归因于遗传疾病的头痛,包括归因于 CADASIL 的头痛。