Makovac Elena, Serra Laura, Spanò Barbara, Giulietti Giovanni, Torso Mario, Cercignani Mara, Caltagirone Carlo, Bozzali Marco
Neuroimaging Laboratory, IRCCS Santa Lucia Foundation, Rome, Italy.
Brighton and Sussex Medical School, Clinical Imaging Sciences Centre, University of Sussex, Brighton, Falmer, UK.
J Alzheimers Dis. 2016;50(2):591-604. doi: 10.3233/JAD-150612.
Behavioral disorders and psychological symptoms (BPSD) in Alzheimer's disease (AD) are known to correlate with grey matter (GM) atrophy and, as shown recently, also with white matter (WM) damage. WM damage and its relationship with GM atrophy are reported in AD, reinforcing the interpretation of the AD pathology in light of a disconnection syndrome. It remains uncertain whether this disconnection might account also for different BPSD observable in AD. Here, we tested the hypothesis of different patterns of association between WM damage of the corpus callosum (CC) and GM atrophy in AD patients exhibiting one of the following BPSD clusters: Mood (i.e., anxiety and depression; ADmood), Frontal (i.e., dishinibition and elation; ADfrontal), and Psychotic (delusions and hallucinations; ADpsychotic) related symptoms, as well as AD patients without BPSD. Overall, this study brings to light the strict relationship between WM alterations in different parts of the CC and GM atrophy in AD patients exhibiting BPSD, supporting the hypothesis that such symptoms are likely to be caused by characteristic patterns of neurodegeneration of WM and GM, rather than being a reactive response to accumulation of cognitive disabilities, and should therefore be regarded as potential markers of diagnostic and prognostic value in AD.
已知阿尔茨海默病(AD)中的行为障碍和心理症状(BPSD)与灰质(GM)萎缩相关,并且最近研究表明,其也与白质(WM)损伤有关。AD中报道了WM损伤及其与GM萎缩的关系,这加强了从失连接综合征角度对AD病理学的解释。目前尚不确定这种失连接是否也能解释AD中观察到的不同BPSD。在此,我们测试了一个假设,即患有以下BPSD集群之一的AD患者,其胼胝体(CC)的WM损伤与GM萎缩之间存在不同的关联模式:情绪(即焦虑和抑郁;AD情绪型)、额叶(即脱抑制和欣快;AD额叶型)以及精神病性(妄想和幻觉;AD精神病性型)相关症状,同时也测试了无BPSD的AD患者。总体而言,本研究揭示了患有BPSD的AD患者CC不同部位的WM改变与GM萎缩之间的紧密关系,支持了这样一种假设,即此类症状可能是由WM和GM的特征性神经退行性变模式引起的,而非对认知障碍积累的反应,因此应被视为AD诊断和预后价值的潜在标志物。