首页> 外文期刊>Neurobiology of Aging: Experimental and Clinical Research >The interaction between sleep-disordered breathing and apolipoprotein E genotype on cerebrospinal fluid biomarkers for Alzheimer's disease in cognitively normal elderly individuals.
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The interaction between sleep-disordered breathing and apolipoprotein E genotype on cerebrospinal fluid biomarkers for Alzheimer's disease in cognitively normal elderly individuals.

机译:睡眠障碍性呼吸与脑脊液生物标志物上载脂蛋白E基因型在认知正常老年人中的阿尔茨海默氏病之间的相互作用。

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摘要

Previous studies have suggested a link between sleep disordered breathing (SDB) and dementia risk. In the present study, we analyzed the relationship between SDB severity, cerebrospinal fluid (CSF) Alzheimer's disease-biomarkers, and the ApoE alleles. A total of 95 cognitively normal elderly participants were analyzed for SDB severity, CSF measures of phosphorylated-tau (p-tau), total-tau (t-tau), and amyloid beta 42 (Aβ-42), as well as ApoE allele status. In ApoE3+ subjects, significant differences were found between sleep groups for p-tau (F[df2] = 4.3, p = 0.017), and t-tau (F[df2] = 3.3, p = 0.043). Additionally, among ApoE3+ subjects, the apnea and/or hypopnea with 4% O2-desaturation index was positively correlated with p-tau (r = 0.30, p = 0.023), t-tau (r = 0.31, p = 0.021), and Aβ-42 (r = 0.31, p = 0.021). In ApoE2+ subjects, the apnea and/or hypopnea with 4% O2-desaturation index was correlated with lower levels of CSF Aβ-42 (r = -0.71, p = 0.004), similarly to ApoE4+ subjects where there was also a trend toward lower CSF Aβ-42 levels. Our observations suggest that there is an association between SDB and CSF Alzheimer's disease-biomarkers in cognitively normal elderly individuals. Existing therapies for SDB such as continuous positive airway pressure could delay the onset to mild cognitive impairment or dementia in normal elderly individuals.
机译:先前的研究表明,睡眠呼吸障碍(SDB)与痴呆风险之间存在联系。在本研究中,我们分析了SDB严重程度,脑脊液(CSF)阿尔茨海默氏病生物标志物和ApoE等位基因之间的关系。总共分析了95名认知正常的老年参与者的SDB严重度,磷酸化tau(p-tau),total-tau(t-tau)和β淀粉样蛋白42(Aβ-42)的CSF测度以及ApoE等位基因状态。在ApoE3 +受试者中,p-tau(F [df2] = 4.3,p = 0.017)和t-tau(F [df2] = 3.3,p = 0.043)的睡眠组之间发现显着差异。此外,在ApoE3 +受试者中,具有2%O2饱和度降低的呼吸暂停和/或呼吸不足与p-tau(r = 0.30,p = 0.023),t-tau(r = 0.31,p = 0.021)和正相关。 Aβ-42(r = 0.31,p = 0.021)。在ApoE2 +受试者中,O2去饱和指数为4%的呼吸暂停和/或呼吸不足与较低的CSFAβ-42水平相关(r = -0.71,p = 0.004),与ApoE4 +受试者也存在降低的趋势脑脊液Aβ-42水平。我们的观察结果表明,在认知正常的老年人中,SDB和脑脊液阿尔茨海默氏病生物标志物之间存在关联。 SDB的现有疗法,例如持续的气道正压通气,可能会延迟正常老年人中轻度认知障碍或痴呆的发作。

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