Graduate Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, Taiwan.
Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.
Hum Brain Mapp. 2018 Jun;39(6):2549-2562. doi: 10.1002/hbm.24022. Epub 2018 Mar 8.
Alzheimer's disease (AD) progresses insidiously from the preclinical stage to dementia. While people with subjective cognitive decline (SCD) have normal cognitive performance, some may be in the preclinical stage of AD. Neurofibrillary tangles appear first in the transentorhinal cortex, followed by the entorhinal cortex in the clinically silent stage of AD. We expected the earliest changes in subjects with SCD to occur in medial temporal subfields other than the hippocampal proper. These selective structural changes would affect specific memory subcomponents. We used the Family Picture subtest of the Wechsler Memory Scale-III, which was modified to separately compute character, activity, and location subscores for episodic memory subcomponents. We recruited 43 subjects with SCD, 44 subjects with amnesic mild cognitive impairment, and 34 normal controls. MRI was used to assess cortical thickness, subcortical gray matter volume, and fractional anisotropy. The results demonstrated that SCD subjects showed significant cortical atrophy in their bilateral parahippocampus and perirhinal and the left entorhinal cortices but not in their hippocampal regions. SCD subjects also exhibited significantly decreased mean fractional anisotropy in their bilateral uncinate fasciculi. The diminution of cortical thickness over the mesial temporal subfields corresponded to brain areas with early tangle deposition, and early degradation of the uncinate fasciculus was in accordance with the retrogenesis hypothesis. The parahippocampus and perirhinal cortex contribute mainly to context association memory while the entorhinal cortex, along with the uncinate fasciculus, contributes to content-related contextual memory. We proposed that context association and related memory structures are vulnerable in the SCD stage.
阿尔茨海默病(AD)从临床前阶段逐渐发展为痴呆。虽然有主观认知下降(SCD)的人认知表现正常,但有些人可能处于 AD 的临床前阶段。神经纤维缠结首先出现在跨颞叶皮质,然后在 AD 的临床无症状阶段出现在内嗅皮质。我们预计 SCD 患者最早的变化将发生在海马体以外的内侧颞叶亚区。这些选择性的结构变化会影响特定的记忆子成分。我们使用了韦氏记忆量表-III 的家庭图片子测验,该测验经过修改,可分别计算情节记忆子成分的字符、活动和位置子分数。我们招募了 43 名 SCD 患者、44 名遗忘性轻度认知障碍患者和 34 名正常对照。使用 MRI 评估皮质厚度、皮质下灰质体积和各向异性分数。结果表明,SCD 患者双侧海马旁回、旁嗅回和左侧内嗅皮质出现明显的皮质萎缩,但海马区没有萎缩。SCD 患者双侧钩束的平均各向异性分数也显著降低。内侧颞叶亚区的皮质厚度减少与早期缠结沉积的脑区相对应,钩束的早期退化与逆行性假说一致。海马旁回和旁嗅回主要参与上下文关联记忆,而内嗅皮质和钩束则参与与内容相关的上下文记忆。我们提出,在 SCD 阶段,上下文关联和相关的记忆结构容易受到影响。