Whitwell Jennifer L, Sampson Elizabeth L, Loy Clement T, Warren Jane E, Rossor Martin N, Fox Nick C, Warren Jason D
Dementia Research Centre, Institute of Neurology, 8-11 Queen Square, London WC1N 3BG, UK.
Neuroimage. 2007 Mar;35(1):207-13. doi: 10.1016/j.neuroimage.2006.12.006. Epub 2007 Jan 19.
The brain bases of specific human behaviours in health and disease are not well established. In this voxel-based morphometric (VBM) study we demonstrate neuroanatomical signatures of different abnormalities of eating behaviour (pathological sweet tooth and increased food consumption, or hyperphagia) in individuals with frontotemporal lobar degeneration (FTLD). Sixteen male patients with FTLD were assessed using the Manchester and Oxford Universities Scale for the Psychopathological Assessment of Dementia and classified according to the presence or absence of abnormal eating behaviours. Volumetric brain magnetic resonance imaging was performed in all patients and in a group of nine healthy age-matched male controls and grey matter changes were assessed using an optimised VBM protocol. Compared with healthy controls, the FTLD group had a typical pattern of extensive bilateral grey matter loss predominantly involving the frontal and temporal lobes. Within the FTLD group, grey matter changes associated with different abnormal behaviours were assessed independently using a covariate-only model. The development of pathological sweet tooth was associated with grey matter loss in a distributed brain network including bilateral posterolateral orbitofrontal cortex (Brodmann areas 12/47) and right anterior insula. Hyperphagia was associated with more focal grey matter loss in anterolateral OFC bilaterally (Brodmann area 11). In accord with emerging evidence in humans and other species, our findings implicate distinct components of a multi-component brain network in the control of specific aspects of eating behaviour.
健康和疾病状态下特定人类行为的脑基础尚未完全明确。在这项基于体素的形态学测量(VBM)研究中,我们展示了额颞叶痴呆(FTLD)患者不同饮食行为异常(病理性嗜甜和食物摄入量增加,即食欲亢进)的神经解剖学特征。16名男性FTLD患者使用曼彻斯特和牛津大学痴呆精神病理学评估量表进行评估,并根据是否存在异常饮食行为进行分类。对所有患者以及一组9名年龄匹配的健康男性对照者进行了脑磁共振成像容积测定,并使用优化的VBM方案评估灰质变化。与健康对照者相比,FTLD组呈现出典型的广泛双侧灰质丢失模式,主要累及额叶和颞叶。在FTLD组内,使用仅含协变量的模型独立评估与不同异常行为相关的灰质变化。病理性嗜甜的发生与包括双侧后外侧眶额皮质(布罗德曼区12/47)和右侧前岛叶在内的分布式脑网络中的灰质丢失有关。食欲亢进与双侧前外侧眶额皮质(布罗德曼区11)更局限的灰质丢失有关。与人类和其他物种的新证据一致,我们的研究结果表明,一个多成分脑网络的不同组成部分参与了饮食行为特定方面的控制。