Department of Radiology, Duke University School of Medicine, Durham, NC, USA.
PLoS One. 2013;8(2):e54483. doi: 10.1371/journal.pone.0054483. Epub 2013 Feb 6.
To investigate whether there is a specific dose-dependent effect of the Apolipoprotein E (APOE) ε4 and ε2 alleles on hippocampal volume, across the cognitive spectrum, from normal aging to Alzheimer's Disease (AD).
We analyzed MR and genetic data on 662 patients from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database-198 cognitively normal controls (CN), 321 mild-cognitive impairment (MCI) subjects, and 143 AD subjects-looking for dose-dependent effects of the ε4 and ε2 alleles on hippocampal volumes. Volumes were measured using a fully-automated algorithm applied to high resolution T1-weighted MR images. Statistical analysis consisted of a multivariate regression with repeated-measures model.
There was a dose-dependent effect of the ε4 allele on hippocampal volume in AD (p = 0.04) and MCI (p = 0.02)-in both cases, each allele accounted for loss of >150 mm(3) (approximately 4%) of hippocampal volume below the mean volume for AD and MCI subjects with no such alleles (Cohen's d = -0.16 and -0.19 for AD and MCI, respectively). There was also a dose-dependent, main effect of the ε2 allele (p<0.0001), suggestive of a moderate protective effect on hippocampal volume-an approximately 20% per allele volume increase as compared to CN with no ε2 alleles (Cohen's d = 0.23).
Though no effect of ε4 was seen in CN subjects, our findings confirm and extend prior data on the opposing effects of the APOE ε4 and ε2 alleles on hippocampal morphology across the spectrum of cognitive aging.
探究载脂蛋白 E(APOE)ε4 和 ε2 等位基因是否对从正常衰老到阿尔茨海默病(AD)的认知谱中的海马体积存在特定的剂量依赖性影响。
我们分析了来自阿尔茨海默病神经影像学倡议(ADNI)数据库的 662 名患者的磁共振成像(MRI)和基因数据,其中包括 198 名认知正常对照(CN)、321 名轻度认知障碍(MCI)患者和 143 名 AD 患者,寻找ε4 和 ε2 等位基因对海马体积的剂量依赖性影响。使用完全自动化的算法对高分辨率 T1 加权 MRI 图像进行测量。统计分析采用多元回归重复测量模型。
ε4 等位基因对 AD(p = 0.04)和 MCI(p = 0.02)患者的海马体积存在剂量依赖性影响,在这两种情况下,每个等位基因导致的海马体积损失超过 150mm³(约 4%),低于无该等位基因的 AD 和 MCI 患者的平均体积(AD 和 MCI 患者的 Cohen's d 值分别为-0.16 和-0.19)。ε2 等位基因也存在剂量依赖性的主要影响(p<0.0001),提示其对海马体积有适度的保护作用,与无 ε2 等位基因的 CN 相比,每个等位基因增加约 20%的体积(Cohen's d 值为 0.23)。
虽然在 CN 受试者中未观察到 ε4 的影响,但我们的发现证实并扩展了先前关于 APOE ε4 和 ε2 等位基因对认知衰老谱中海马形态的相反影响的数据。