Juottonen K, Lehtovirta M, Helisalmi S, Riekkinen P J, Soininen H
Department of Neuroscience and Neurology, University of Kuopio, Finland.
J Neurol Neurosurg Psychiatry. 1998 Sep;65(3):322-7. doi: 10.1136/jnnp.65.3.322.
Recent evidence indicates that the apolipoprotein E (ApoE) epsilon4 allele is a risk factor for developing Alzheimer's disease. It has also been proposed that it is associated with increased counts of amyloid plaques and neurofibrillary tangles that in turn are neuropathological hallmarks initially appearing in the medial temporal lobe structures in Alzheimer's disease. In this study, the effect of the ApoE epsilon4 allele on the volume of the entorhinal cortex was evaluated in vivo.
The volume of the entorhinal cortex was measured on MR images using a recently designed histology based protocol in 16 patients with Alzheimer's disease with ApoE epsilon4 (mean age 70.4 (SD 9.9)), 11 patients with Alzheimer's disease without ApoE epsilon4 (mean age 69.1 (SD7.1)), and in 31 healthy age and sex matched normal controls (72.2 (SD 3.9)). The patients met the NINCDS-ADRDA criteria for probable Alzheimer's disease and were in mild to moderate stages of the disease. MRI was performed with a 1.5 Tesla Magnetom and a 3D technique permitting the reconstruction of 2.0 mm thick contiguous slices perpendicular to the axis of the anterior-posterior commissure.
The patients with Alzheimer's disease without the ApoE epsilon4 allele had atrophy in the entorhinal cortex, the volume was reduced by 27% compared with control subjects. However, the most prominent shrinkage (45%) in the entorhinal cortex was seen in patients with Alzheimer's disease with the ApoE epsilon4 allele (p=0.0001). The effect of epsilon4 on the entorhinal cortex volume was especially prominent in female patients with Alzheimer's disease compared to male patients with Alzheimer's disease (p=0.014). Additionally, patients with the ApoE epsilon4 allele had inferior performance in verbal and visual memory functions than those without the allele
Volumetric MRI measurements disclose that ApoE epsilon4 is associated with the degree of atrophy in the entorhinal cortex in early Alzheimer's disease, this effect being especially prominent in female patients with Alzheimer's disease.
最近的证据表明,载脂蛋白E(ApoE)ε4等位基因是患阿尔茨海默病的一个风险因素。也有人提出,它与淀粉样斑块和神经原纤维缠结数量的增加有关,而这些反过来又是阿尔茨海默病最初出现在内侧颞叶结构中的神经病理学特征。在本研究中,在活体状态下评估了ApoE ε4等位基因对内嗅皮质体积的影响。
使用最近设计的基于组织学的方案,在16例携带ApoE ε4的阿尔茨海默病患者(平均年龄70.4(标准差9.9))、11例不携带ApoE ε4的阿尔茨海默病患者(平均年龄69.1(标准差7.1))以及31名年龄和性别匹配的健康正常对照者(72.2(标准差3.9))的磁共振图像上测量内嗅皮质的体积。这些患者符合NINCDS - ADRDA可能的阿尔茨海默病标准,且处于疾病的轻度至中度阶段。使用1.5特斯拉的Magnetom磁共振成像仪和一种3D技术进行磁共振成像,该技术允许重建垂直于前后连合轴的2.0毫米厚的连续切片。
不携带ApoE ε4等位基因的阿尔茨海默病患者存在内嗅皮质萎缩,其体积与对照受试者相比减少了27%。然而,携带ApoE ε4等位基因的阿尔茨海默病患者的内嗅皮质萎缩最为明显(45%)(p = 0.0001)。与携带ApoE ε4等位基因的男性阿尔茨海默病患者相比,ε4对女性阿尔茨海默病患者内嗅皮质体积的影响尤为显著(p = 0.014)。此外,携带ApoE ε4等位基因的患者在言语和视觉记忆功能方面的表现比不携带该等位基因的患者差。
体积磁共振成像测量结果显示,ApoE ε4与早期阿尔茨海默病内嗅皮质的萎缩程度相关,这种影响在女性阿尔茨海默病患者中尤为显著。