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Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length

机译:亨廷顿病发病年龄:载脂蛋白E基因型和正常CAG重复长度的性别特异性影响

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摘要

Age of onset (AO) of Huntington disease (HD) is known to be correlated with the length of an expanded CAG repeat in the HD gene. Apolipoprotein E (APOE) genotype, in turn, is known to influence AO in Alzheimer disease, rendering the APOE gene a likely candidate to affect AO in other neurological diseases too. We therefore determined APOE genotype and normal CAG repeat length in the HD gene for 138 HD patients who were previously analysed with respect to CAG repeat length. Genotyping for APOE was performed blind to clinical information. In addition to highlighting the effect of the normal repeat length upon AO in maternally inherited HD and in male patients, we show that the APOE ε2ε3 genotype is associated with significantly earlier AO in males than in females. Such a sex difference in AO was not apparent for any of the other APOE genotypes. Our findings suggest that subtle differences in the course of the neurodegeneration in HD may allow interacting genes to exert gender specific effects upon AO.


Keywords: Huntington disease; APOE; age of onset
机译:已知亨廷顿病(HD)的发病年龄(AO)与HD基因中扩展的CAG重复序列的长度相关。反过来,载脂蛋白E(APOE)基因型会影响阿尔茨海默氏病中的AO,从而使APOE基因也可能在其他神经系统疾病中影响AO。因此,我们确定了138位HD患者的HD基因中APOE基因型和正常CAG重复长度,这些患者先前已进行过CAG重复长度分析。对APOE进行基因分型对临床信息不了解。除了在母本遗传的HD和男性患者中突出正常重复长度对AO的影响外,我们还显示,男性的APOEε2ε3基因型与女性的AO显着相关。对于其他任何APOE基因型,在AO中的性别差异均不明显。我们的研究结果表明,高清神经变性过程中的细微差异可能使相互作用的基因对AO发挥性别特异性作用。


APOE;发病年龄

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