Aridon P, D'Andrea G, Rigamonti A, Leone M, Casari G, Bussone G
Human Molecular Genetics Unit, DIBIT-San Raffaele Scientific Institute, Milan, Italy.
Neurol Sci. 2004 Oct;25 Suppl 3:S279-80. doi: 10.1007/s10072-004-0309-1.
Cluster headache (CH) is characterised by unilateral pain and ipsilateral autonomic features. To date, no molecular genetic evidence has been shown for CH. Small pedigrees and low penetrance render the identification of the CH-gene quite difficult. Nonetheless the association of CH and migraine to a new class of amine, namely trace or elusive amines such as tyramine, octopamine and synephrine, has recently been demonstrated. In particular, in comparison to healthy control subjects, all these neurotransmitters have been found to be greatly elevated in CH sufferers in plasma and platelets both in active and remission periods. A cluster of gene-encoding G-protein-coupled receptors that bind and are activated by trace amines was identified in the long arm of chromosome 6q23. We evaluated two families with CH by linkage analysis to 6q23 region and the mutation scanning of the TAR 1, TAR 3, TAR 4, TAR 5, PNR and GPR58 genes by denaturing high liquid chromatography is in progress in 16 familial cases.
丛集性头痛(CH)的特点是单侧疼痛和同侧自主神经症状。迄今为止,尚未有CH的分子遗传学证据。小家系和低外显率使得CH相关基因的鉴定颇具难度。尽管如此,最近已证实CH和偏头痛与一类新的胺类物质有关,即微量或难以捉摸的胺类,如酪胺、章鱼胺和辛弗林。特别是,与健康对照受试者相比,在CH患者的血浆和血小板中,无论是在发作期还是缓解期,所有这些神经递质的水平都显著升高。在6号染色体长臂6q23上发现了一组编码与微量胺结合并被其激活的G蛋白偶联受体的基因。我们通过对6q23区域的连锁分析评估了两个患有CH的家系,并且正在对16个家族性病例进行变性高效液相色谱法对TAR 1、TAR 3、TAR 4、TAR 5、PNR和GPR58基因的突变扫描。