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潜在类别和遗传分析并不支持将伴先兆偏头痛和无先兆偏头痛视为独立的实体。

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities.

作者信息

Nyholt Dale R, Gillespie Nathan G, Heath Andrew C, Merikangas Kathleen R, Duffy David L, Martin Nicholas G

机构信息

Queensland Institute of Medical Research, Brisbane, Queensland, Australia.

出版信息

Genet Epidemiol. 2004 Apr;26(3):231-44. doi: 10.1002/gepi.10311.

Abstract

Latent class and genetic analyses were used to identify subgroups of migraine sufferers in a community sample of 6,265 Australian twins (55% female) aged 25-36 who had completed an interview based on International Headache Society (IHS) criteria. Consistent with prevalence rates from other population-based studies, 703 (20%) female and 250 (9%) male twins satisfied the IHS criteria for migraine without aura (MO), and of these, 432 (13%) female and 166 (6%) male twins satisfied the criteria for migraine with aura (MA) as indicated by visual symptoms. Latent class analysis (LCA) of IHS symptoms identified three major symptomatic classes, representing 1) a mild form of recurrent nonmigrainous headache, 2) a moderately severe form of migraine, typically without visual aura symptoms (although 40% of individuals in this class were positive for aura), and 3) a severe form of migraine typically with visual aura symptoms (although 24% of individuals were negative for aura). Using the LCA classification, many more individuals were considered affected to some degree than when using IHS criteria (35% vs. 13%). Furthermore, genetic model fitting indicated a greater genetic contribution to migraine using the LCA classification (heritability, h(2)=0.40; 95% CI, 0.29-0.46) compared with the IHS classification (h(2)=0.36; 95% CI, 0.22-0.42). Exploratory latent class modeling, fitting up to 10 classes, did not identify classes corresponding to either the IHS MO or MA classification. Our data indicate the existence of a continuum of severity, with MA more severe but not etiologically distinct from MO. In searching for predisposing genes, we should therefore expect to find some genes that may underlie all major recurrent headache subtypes, with modifying genetic or environmental factors that may lead to differential expression of the liability for migraine.

摘要

采用潜在类别分析和基因分析,在一个由6265名年龄在25 - 36岁的澳大利亚双胞胎(55%为女性)组成的社区样本中,识别偏头痛患者的亚组。这些双胞胎完成了一项基于国际头痛协会(IHS)标准的访谈。与其他基于人群的研究患病率一致,703名(20%)女性和250名(9%)男性双胞胎符合IHS无先兆偏头痛(MO)标准,其中,432名(13%)女性和166名(6%)男性双胞胎符合有视觉症状所指示的有先兆偏头痛(MA)标准。对IHS症状进行潜在类别分析(LCA),确定了三个主要症状类别,分别代表:1)轻度复发性非偏头痛性头痛;2)中度严重的偏头痛形式,通常无视觉先兆症状(尽管该类别中40%的个体有先兆阳性);3)严重的偏头痛形式,通常有视觉先兆症状(尽管24%的个体无先兆)。使用LCA分类法,与使用IHS标准相比,更多个体在某种程度上被认为受影响(35%对13%)。此外,基因模型拟合表明,与IHS分类(遗传度,h(2)=0.36;95%可信区间,0.22 - 0.42)相比,使用LCA分类法时偏头痛的遗传贡献更大(遗传度,h(2)=0.40;95%可信区间,0.29 - 0.46)。探索性潜在类别建模,拟合多达10个类别,未识别出与IHS的MO或MA分类相对应的类别。我们的数据表明存在严重程度的连续体,MA更严重但在病因上与MO无明显差异。因此,在寻找易感基因时,我们应该期望找到一些可能是所有主要复发性头痛亚型基础的基因,以及可能导致偏头痛易感性差异表达的修饰基因或环境因素。

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