Department of Psychiatry and Psychotherapy, Heinrich-Heine-University, Duesseldorf, Germany.
Psychiatry Res. 2010 Jul 30;183(1):44-51. doi: 10.1016/j.pscychresns.2010.04.003. Epub 2010 Jun 11.
The spatial and temporal relations between regional cerebral blood flow (rCBF) and brain volume (rVOL) changes in incipient and early Alzheimer's dementia (AD) are not fully understood. The participants comprised 30 subjects with mild cognitive impairment (MCI) and 15 with mild AD who were examined using structural and perfusion-weighted magnetic resonance imaging (MRI) at 1.5 Tesla. Hippocampus and amygdala volumes were measured by manual volumetry. A region-of-interest co-localisation method was used to calculate rCBF values. DNA samples were genotyped for apolipoprotein E (APO E). In comparisons of AD with MCI, rCBF was reduced in the posterior cingulum only, while profound rVOL reductions occurred in both right and left amygdala and in the right hippocampus, and as a trend, in the left hippocampus. Brain volumes of the hippocampus and the amygdala were uncorrelated with the respective rCBF variables in both MCI and AD. Hippocampal but not amygdalar volumes were associated with presence of one or two APOE epsilon4 alleles in MCI and mild AD, while there was no association of APOE epsilon4 allele with rCBF. These data support earlier indications that rCBF and rVOL changes are at least partly dissociated in the early pathogenesis of AD and heterogeneously associated with the APOE risk allele. The data also support the concept of functional compensatory brain activation and the diaschisis hypothesis as relevant in incipient and early AD.
在早期阿尔茨海默病(AD)中,区域性脑血流(rCBF)和脑体积(rVOL)变化之间的时空关系尚不完全清楚。本研究纳入了 30 名轻度认知障碍(MCI)患者和 15 名轻度 AD 患者,他们在 1.5T 磁共振扫描仪上接受了结构和灌注加权磁共振成像(MRI)检查。使用手动体积测量法测量海马体和杏仁核的体积。采用感兴趣区定位方法计算 rCBF 值。对载脂蛋白 E(APO E)进行 DNA 分型。在 AD 与 MCI 的比较中,仅后扣带回的 rCBF 降低,而双侧杏仁核和右侧海马体的 rVOL 显著降低,左侧海马体也呈降低趋势。在 MCI 和 AD 中,海马体和杏仁核的脑体积与相应的 rCBF 变量均无相关性。在 MCI 和轻度 AD 中,只有海马体体积与一个或两个 APO E epsilon4 等位基因相关,而杏仁核体积与 APO E epsilon4 等位基因无关。这些数据支持了更早的提示,即 rCBF 和 rVOL 变化在 AD 的早期发病机制中至少部分分离,并且与 APOE 风险等位基因呈异质性相关。这些数据还支持功能性补偿性大脑激活和神经传递障碍假说在早期 AD 中的相关性。