Dementia Research Centre, Institute of Neurology, University College London, Queen Square, London, UK.
J Alzheimers Dis. 2012;30(2):407-11. doi: 10.3233/JAD-2012-111556.
Frontotemporal lobar degeneration (FTLD) is a neurodegenerative disorder which presents with either behavioral or language impairment. The two language syndromes are known as progressive nonfluent aphasia (PNFA) and semantic dementia (SEMD). While cross-sectional imaging patterns of brain atrophy are well-described in FTLD, fewer studies have investigated longitudinal imaging changes. We measured longitudinal hemispheric and lobar atrophy rates using serial MRI in a cohort of 18 patients with PNFA and 17 patients with SEMD as well as 14 cognitively-normal control subjects. We subsequently calculated sample size estimates for clinical trials. Rates of left hemisphere atrophy were greater than rates of right hemisphere atrophy in both PNFA and SEMD with no significant differences between the groups. The disease groups showed asymmetrical atrophy (more severe on the left) at baseline with significantly increasing asymmetry over time. Within a hemisphere, the fastest rate of atrophy varied between lobes: in SEMD temporal > frontal > parietal > occipital, while in PNFA frontal > temporal/parietal > occipital. In SEMD, using temporal lobe measures of atrophy in clinical trials would provide the lowest sample sizes necessary, while in PNFA left hemisphere atrophy measures provided the lowest sample size. These patterns provide information about disease evolution in the FTLD language variants that is of both clinical and neurobiological relevance.
额颞叶变性(FTLD)是一种神经退行性疾病,表现为行为或语言障碍。两种语言综合征分别称为进行性非流利性失语症(PNFA)和语义性痴呆症(SEMD)。虽然 FTLD 的大脑萎缩的横断面成像模式已有很好的描述,但研究纵向成像变化的较少。我们在 18 名 PNFA 患者和 17 名 SEMD 患者以及 14 名认知正常的对照组中使用连续 MRI 测量了纵向半球和脑叶萎缩率。随后,我们计算了临床试验的样本量估计。在 PNFA 和 SEMD 中,左半球的萎缩率均大于右半球的萎缩率,但两组之间无显著差异。疾病组在基线时表现出不对称性萎缩(左侧更严重),随着时间的推移,不对称性显著增加。在一个半球内,萎缩最快的部位在不同的脑叶之间有所不同:在 SEMD 中,颞叶>额叶>顶叶>枕叶,而在 PNFA 中,额叶>颞叶/顶叶>枕叶。在 SEMD 中,在临床试验中使用颞叶萎缩的指标可以提供最低的样本量,而在 PNFA 中,左半球萎缩的指标提供了最低的样本量。这些模式提供了与 FTLD 语言变异体相关的临床和神经生物学意义的疾病演变信息。