Nyholt Dale R, Morley Katherine I, Ferreira Manuel A R, Medland Sarah E, Boomsma Dorret I, Heath Andrew C, Merikangas Kathleen R, Montgomery Grant W, Martin Nicholas G
Queensland Institute of Medical Research, Brisbane, Australia.
Am J Hum Genet. 2005 Sep;77(3):500-12. doi: 10.1086/444510. Epub 2005 Jul 28.
Familial typical migraine is a common, complex disorder that shows strong familial aggregation. Using latent-class analysis (LCA), we identified subgroups of people with migraine/severe headache in a community sample of 12,245 Australian twins (60% female), drawn from two cohorts of individuals aged 23-90 years who completed an interview based on International Headache Society criteria. We report results from genomewide linkage analyses involving 756 twin families containing a total of 790 independent sib pairs (130 affected concordant, 324 discordant, and 336 unaffected concordant for LCA-derived migraine). Quantitative-trait linkage analysis produced evidence of significant linkage on chromosome 5q21 and suggestive linkage on chromosomes 8, 10, and 13. In addition, we replicated previously reported typical-migraine susceptibility loci on chromosomes 6p12.2-p21.1 and 1q21-q23, the latter being within 3 cM of the rare autosomal dominant familial hemiplegic migraine gene (ATP1A2), a finding which potentially implicates ATP1A2 in familial typical migraine for the first time. Linkage analyses of individual migraine symptoms for our six most interesting chromosomes provide tantalizing hints of the phenotypic and genetic complexity of migraine. Specifically, the chromosome 1 locus is most associated with phonophobia; the chromosome 5 peak is predominantly associated with pulsating headache; the chromosome 6 locus is associated with activity-prohibiting headache and photophobia; the chromosome 8 locus is associated with nausea/vomiting and moderate/severe headache; the chromosome 10 peak is most associated with phonophobia and photophobia; and the chromosome 13 peak is completely due to association with photophobia. These results will prove to be invaluable in the design and analysis of future linkage and linkage disequilibrium studies of migraine.
家族性典型偏头痛是一种常见的复杂疾病,具有很强的家族聚集性。我们采用潜在类别分析(LCA),在一个由12245名澳大利亚双胞胎(60%为女性)组成的社区样本中,识别出偏头痛/严重头痛患者亚组。这些双胞胎来自两个年龄在23至90岁的队列,他们根据国际头痛协会标准完成了一次访谈。我们报告了全基因组连锁分析的结果,该分析涉及756个双胞胎家庭,共790个独立同胞对(130对受影响一致、324对不一致、336对LCA衍生偏头痛未受影响一致)。数量性状连锁分析在5号染色体q21区域产生了显著连锁的证据,在8号、10号和13号染色体上产生了提示性连锁的证据。此外,我们在6号染色体上12.2 - p21.1区域和1号染色体上q21 - q23区域重复了先前报道的典型偏头痛易感位点,后者位于罕见的常染色体显性家族性偏瘫性偏头痛基因(ATP1A2)的3厘摩范围内,这一发现首次潜在地表明ATP1A2与家族性典型偏头痛有关。对我们最感兴趣的6条染色体上的个体偏头痛症状进行连锁分析,为偏头痛的表型和遗传复杂性提供了诱人线索。具体而言,1号染色体位点与畏声最相关;5号染色体峰值主要与搏动性头痛相关;6号染色体位点与限制活动的头痛和畏光相关;8号染色体位点与恶心/呕吐及中度/重度头痛相关;10号染色体峰值与畏声和畏光最相关;13号染色体峰值完全是由于与畏光相关。这些结果在未来偏头痛的连锁和连锁不平衡研究的设计与分析中将被证明具有极高价值。