Barbas Nancy R, Schuyler Erica A
Department of Neurology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Semin Neurol. 2006 Nov;26(5):507-14. doi: 10.1055/s-2006-951623.
It is well recognized that headache, and especially migraine, runs in families. Recent studies into the heritability of primary headache subtypes, migraine, cluster and tension headache, and conditions in which headache is a prominent feature, such as the mitochondrial disease, mitochondrial encephalopathy, lactic acidosis, and strokelike episodes, and the arteriopathy, cerebral autosomal-dominant arteriopathy with subcortical infarctions and leukoencephalopathy, are improving our understanding of the genetic contribution to headache. Studies of the rare familial hemiplegic migraine are leading to advances in understanding the pathophysiological mechanisms of the more common migraine types. Current knowledge of hereditary and genetic features of headache subtypes is reviewed and the implications for understanding the pathophysiology of migraine are discussed.
众所周知,头痛,尤其是偏头痛,具有家族遗传性。最近对原发性头痛亚型(偏头痛、丛集性头痛和紧张性头痛)以及以头痛为突出特征的疾病(如线粒体疾病、线粒体脑肌病、乳酸酸中毒和卒中样发作)和动脉病(伴有皮质下梗死和白质脑病的大脑常染色体显性动脉病)的遗传度研究,正在加深我们对头痛遗传因素的理解。对罕见的家族性偏瘫性偏头痛的研究正在推动对更常见偏头痛类型病理生理机制的认识。本文综述了目前关于头痛亚型的遗传和基因特征的知识,并讨论了其对理解偏头痛病理生理学的意义。