From the Department of Clinical Neurosciences (E.J.Y., Z.I., A.H., M.K., T.H., J.C., I.K., J.R.S., D.M., S.F., O.M.) and Departments of Psychiatry and Community Health Sciences (Z.I.), University of Calgary; Hotchkiss Brain Institute (E.J.Y., Z.I., A.H., M.K., T.H., J.C., I.K., J.R.S., D.M., S.F., O.M.), Cumming School of Medicine, Calgary, Alberta; Centre de Recherche (A.H., O.M.), Institut Universitaire de Gériatrie de Montréal; and Department of Psychology (A.H.), University of Montréal, Québec, Canada.
Neurology. 2019 Aug 20;93(8):e766-e777. doi: 10.1212/WNL.0000000000007968. Epub 2019 Jul 18.
To evaluate the associations of mild behavioral impairment (MBI) with cognitive deficits and patterns of gray matter changes in Parkinson disease (PD).
Sixty patients with PD without dementia and 29 healthy controls underwent a cognitive neuropsychological evaluation and structural MRI scan. MBI was evaluated with the MBI Checklist (MBI-C), a rating scale designed to elicit emergent neuropsychiatric symptoms in accordance with MBI criteria. We divided the patients with PD into 2 groups: 1 group with high MBI-C scores (PD-MBI) and the other with low MBI-C scores (PD-noMBI).
Among 60 patients with PD, 20 were categorized as having PD-MBI (33.33%). In healthy controls, no participants met the MBI cut-point threshold. The PD-MBI group had significantly lower Montreal Cognitive Assessment and scores in all 5 domains and the global score compared to healthy controls and those with PD-noMBI. In addition, all cognitive domains except language and global cognition negatively correlated with the MBI-C total score in all patients with PD. For cortical structures, the PD-MBI group revealed middle temporal cortex thinning and decreased volume compared with the PD-noMBI group, and decreased volume in this area negatively correlated with the MBI-C total score.
The impaired cognitive function over all domains and atrophy in the temporal area in the PD-MBI group are in line with posterior cortical circuit deficits in PD, which have been associated with a faster rate of progression to dementia. These initial results suggest that MBI might be an early and important marker for incident cognitive decline and dementia in patients with PD.
评估轻度行为障碍(MBI)与帕金森病(PD)认知缺陷和灰质变化模式的相关性。
60 名无痴呆的 PD 患者和 29 名健康对照者接受了认知神经心理学评估和结构 MRI 扫描。使用 MBI 检查表(MBI-C)评估 MBI,该量表旨在根据 MBI 标准引出新出现的神经精神症状。我们将 PD 患者分为 2 组:MBI-C 评分高(PD-MBI)组和 MBI-C 评分低(PD-noMBI)组。
在 60 名 PD 患者中,有 20 名患者被归类为 PD-MBI(33.33%)。在健康对照组中,没有参与者达到 MBI 截断阈值。与健康对照组和 PD-noMBI 组相比,PD-MBI 组的蒙特利尔认知评估和所有 5 个领域以及总体评分明显较低。此外,除语言和总体认知外,所有认知领域与所有 PD 患者的 MBI-C 总分呈负相关。对于皮质结构,PD-MBI 组与 PD-noMBI 组相比,颞叶中部皮质变薄,体积减小,而该区域的体积与 MBI-C 总分呈负相关。
PD-MBI 组所有领域的认知功能受损和颞区萎缩与 PD 后皮质回路缺陷一致,后者与向痴呆进展的速度较快有关。这些初步结果表明,MBI 可能是 PD 患者认知能力下降和痴呆发生的早期重要标志物。