Hirjak Dusan, Wolf Robert C, Pfeifer Barbara, Kubera Katharina M, Thomann Anne K, Seidl Ulrich, Maier-Hein Klaus H, Schröder Johannes, Thomann Philipp A
Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University Mannheim, Germany; Center for Psychosocial Medicine, Department of General Psychiatry, University of Heidelberg, Germany.
Center for Psychosocial Medicine, Department of General Psychiatry, University of Heidelberg, Germany.
J Psychiatr Res. 2017 Jul;90:133-142. doi: 10.1016/j.jpsychires.2017.02.019. Epub 2017 Feb 22.
It is unclear whether clock drawing test (CDT) performance relies on a widely distributed cortical network, or whether this test predominantly taps into parietal cortex function. So far, associations between cortical integrity and CDT impairment in Alzheimer's disease (AD) and mild cognitive impairment (MCI) largely stem from cortical volume analyses. Given that volume is a product of thickness and surface area, investigation of the relationship between CDT and these two cortical measures might contribute to better understanding of this cognitive screening tool for AD. 38 patients with AD, 38 individuals with MCI and 31 healthy controls (HC) underwent CDT assessment and MRI at 3 Tesla. The surface-based analysis via Freesurfer enabled calculation of cortical thickness and surface area. CDT was scored according to the method proposed by Shulman and related to the two distinct cortical measurements. Higher CDT scores across the entire sample were associated with cortical thickness in bilateral temporal gyrus, the right supramarginal gyrus, and the bilateral parietal gyrus, respectively (p < 0.001 CWP corr.). Significant associations between CDT and cortical thickness reduction in the parietal lobe remained significant when analyses were restricted to AD individuals. There was no statistically significant association between CDT scores and surface area (p < 0.001 CWP corr.). In conclusion, CDT performance may be driven by cortical thickness alterations in regions previously identified as "AD vulnerable", i.e. regions predominantly including temporal and parietal lobes. Our results suggest that cortical features of distinct evolutionary and genetic origin differently contribute to CDT performance.
目前尚不清楚画钟试验(CDT)的表现是否依赖于广泛分布的皮质网络,或者该测试是否主要利用顶叶皮质功能。到目前为止,阿尔茨海默病(AD)和轻度认知障碍(MCI)中皮质完整性与CDT损害之间的关联主要源于皮质体积分析。鉴于体积是厚度和表面积的乘积,研究CDT与这两种皮质测量之间的关系可能有助于更好地理解这种AD认知筛查工具。38例AD患者、38例MCI个体和31名健康对照(HC)接受了3特斯拉的CDT评估和MRI检查。通过Freesurfer进行基于表面的分析,能够计算皮质厚度和表面积。CDT根据舒尔曼提出的方法进行评分,并与两种不同的皮质测量相关。整个样本中较高的CDT分数分别与双侧颞回、右侧缘上回和双侧顶叶回的皮质厚度相关(p < 0.001 CWP校正)。当分析仅限于AD个体时,CDT与顶叶皮质厚度减少之间的显著关联仍然显著。CDT分数与表面积之间没有统计学上的显著关联(p < 0.001 CWP校正)。总之,CDT表现可能由先前确定为“AD易损”区域的皮质厚度改变驱动,即主要包括颞叶和顶叶的区域。我们的结果表明,具有不同进化和遗传起源的皮质特征对CDT表现的贡献不同。