Kril Jillian J, Macdonald Virginia, Patel Smita, Png Francoise, Halliday Glenda M
Centre for Education and Research on Ageing, The University of Sydney, Concord Hospital, Concord 2139, Sydney, Australia.
J Neurol Sci. 2005 May 15;232(1-2):83-90. doi: 10.1016/j.jns.2005.02.003.
Marked brain atrophy occurs in frontotemporal dementia (FTD) yet substantial variation between cases is seen. Recently, a four-level staging scheme which reflects increasing disease duration, severity of dementia and degree of neurodegeneration was described. In the present study, the extent and magnitude of atrophy in behavioral variant FTD and its relationship to disease duration and pathological subtype was further evaluated by quantifying the volume of 30 anatomically-defined regions. A validated point count technique was applied to 17 patients with FTD (9 Pick's disease, 6 dementia lacking distinctive histology, 2 FTD with motor neuron disease) and 21 controls. Atrophy was seen in all brain regions except the inferior frontal cortex and area 37. As might be expected, increasing severity of atrophy occurred with increasing disease duration and stage however measurable atrophy was more widespread than indicated by the staging scheme. Furthermore, severity of atrophy was not related to pathological subtype. Frontal, limbic and temporal regions appeared to be severely affected early in the disease process with temporal lobe atrophy the best predictor of disease duration. White matter, more posterior regions and the subcortex were affected later in the disease. These findings demonstrate a pattern of selective vulnerability which progresses over time. Furthermore, they demonstrate that although patients with a similar clinical subtype may have differing underlying histopathology, the pattern, severity and progression of brain atrophy is the same. This suggests that the regional pattern of neurodegeneration, rather than the type of histopathology influences the clinical syndrome in FTD.
额颞叶痴呆(FTD)会出现明显的脑萎缩,但病例之间存在显著差异。最近,有人描述了一种四级分期方案,该方案反映了疾病持续时间的增加、痴呆的严重程度和神经退行性变的程度。在本研究中,通过量化30个解剖学定义区域的体积,进一步评估了行为变异型FTD的萎缩程度及其与疾病持续时间和病理亚型的关系。对17例FTD患者(9例匹克病、6例无明显组织学特征的痴呆、2例合并运动神经元病的FTD)和21名对照者应用了一种经过验证的点计数技术。除额下回皮质和37区外,所有脑区均出现萎缩。正如预期的那样,萎缩严重程度随着疾病持续时间和分期的增加而增加,然而可测量的萎缩比分期方案所示更为广泛。此外,萎缩严重程度与病理亚型无关。额叶、边缘叶和颞叶区域在疾病过程早期似乎受到严重影响,其中颞叶萎缩是疾病持续时间的最佳预测指标。白质、更靠后的区域和皮质下区域在疾病后期受到影响。这些发现表明了一种随时间推移而进展的选择性易损模式。此外,它们表明,尽管临床亚型相似的患者可能有不同的潜在组织病理学,但脑萎缩的模式、严重程度和进展是相同的。这表明神经退行性变的区域模式而非组织病理学类型影响了FTD的临床综合征。