Department of Neurology, Sungkyunkwan University School of Medicine, Seoul, Korea.
Sleep. 2011 Oct 1;34(10):1357-64. doi: 10.5665/SLEEP.1278.
To investigate differences in cortical thickness in narcolepsy patients with cataplexy and control subjects.
Cortical thickness was measured using a 3-D surface-based method that enables more accurate measurement in deep sulci and localized regional mapping.
University hospital.
We enrolled 28 patients with narcolepsy and cataplexy and 33 age-and sex-matched control subjects.
Cortical thickness was measured using a direct method for calculating the distance between corresponding vertices from inner and outer cortical surfaces.
We normalized cortical surfaces using 2-D surface registration and performed diffusion smoothing to reduce the variability of folding patterns and to increase the power of the statistical analysis. Localized cortical thinning in narcolepsy patients with cataplexy was found in orbitofrontal gyri, dorsolateral and medial prefrontal cortexes, insula, cingulate gyri, middle and inferior temporal gyri, and inferior parietal lobule of the right and left hemispheres at the level of a false discovery rate P<0.05. No significant local increases in cortical thickness were observed in narcolepsy patients. A significant negative correlation was observed between the narcolepsy patients' scores on the Epworth Sleepiness Scale and the cortical thickness of the left supramarginal gyrus.
Cortical thinning in narcolepsy patients with cataplexy in localized anatomic brain regions may serve as a possible neuroanatomic mechanism of the disturbances in attention, memory, emotion, and sleepiness.
研究伴猝倒的发作性睡病患者与对照受试者皮质厚度的差异。
采用 3D 表面法测量皮质厚度,该方法可更准确地测量深部脑沟和局部区域图谱。
大学医院。
我们纳入了 28 例伴猝倒的发作性睡病患者和 33 例年龄和性别匹配的对照受试者。
采用直接方法测量皮质厚度,该方法计算内、外皮质表面相应顶点之间的距离。
我们使用 2D 表面配准对皮质表面进行归一化,并进行扩散平滑处理,以减少折叠模式的可变性,并提高统计分析的功效。在伴猝倒的发作性睡病患者中,发现右半球和左半球额眶回、背外侧和内侧前额叶皮质、岛叶、扣带回、中颞和下颞回以及下顶叶存在局部皮质变薄,在假发现率 P<0.05 水平。在发作性睡病患者中未观察到皮质厚度的显著局部增加。发作性睡病患者的 Epworth 嗜睡量表评分与左侧缘上回皮质厚度呈显著负相关。
伴猝倒的发作性睡病患者在局部解剖脑区的皮质变薄可能是注意力、记忆、情绪和嗜睡障碍的潜在神经解剖学机制。