From the Departments of Neurology (S.W.K., H.S.Y., S.J.C., P.H.L., Y.H.S., B.S.Y.) and Nuclear Medicine (M.Y.), Yonsei University College of Medicine, Seoul, Korea; and McGill Centre for Integrative Neuroscience (S.J., A.C.E.), Montreal Neurological Institute, McGill University, Quebec, Canada.
Neurology. 2019 Apr 23;92(17):e2015-e2026. doi: 10.1212/WNL.0000000000007373. Epub 2019 Apr 3.
To investigate the independent and interaction effects of Alzheimer disease (AD) and Lewy body disease (LBD) on cognition and brain atrophy.
We consecutively recruited 38 controls and 108 patients with AD-related cognitive impairment (ADCI) and/or LBD-related cognitive impairment (LBCI) from university-based dementia and movement clinics. Diagnoses of ADCI and LBCI were supported by F-florbetaben PET and F-N-(3-fluoropropyl)-2β-carbon ethoxy-3β-(4-iodophenyl) nortropane-PET, respectively. There were 38 controls, 26 patients with pure ADCI (18 mild cognitive impairment [MCI] and 8 dementia), 28 patients with pure LBCI (13 MCI and 15 dementia), and 54 patients with mixed ADCI and LBCI (17 MCI and 37 dementia). We performed group-wise comparisons for neuropsychological scores and regional cortical thickness. We also evaluated the effects of ADCI and LBCI using general linear models.
Compared to the controls, patients in the pure ADCI group and pure LBCI group had focused cortical thinning in the bilateral entorhinal/right anterior temporal cortices and bilateral anteromedial temporal/basal frontal cortices, respectively, while the mixed disease group had additional cortical thinning in the widespread association cortices. The independent effects of ADCI and LBCI on regional cortical thinning overlapped in the widespread association cortices, especially at the bilateral temporoparietal junction and parietal cortices. ADCI and LBCI had independent detrimental effects on the copying item of the Rey-Osterrieth Complex Figure Test.
Concomitant ADCI and LBCI are associated with the accentuation of neurodegeneration to widespread association cortices, and both diseases contribute to visuospatial dysfunction.
研究阿尔茨海默病(AD)和路易体病(LBD)对认知和脑萎缩的独立和交互作用。
我们连续招募了 38 名对照者和 108 名 AD 相关认知障碍(ADCI)和/或 LBD 相关认知障碍(LBCI)患者,这些患者来自大学附属的痴呆和运动诊所。ADCI 和 LBCI 的诊断分别得到 F-氟比苯丙胺 PET 和 F-N-(3-氟丙基)-2β-碳乙氧基-3β-(4-碘苯基)去甲托烷-PET 的支持。有 38 名对照者,26 名单纯 ADCI 患者(18 名轻度认知障碍[MCI]和 8 名痴呆),28 名单纯 LBCI 患者(13 名 MCI 和 15 名痴呆),54 名混合 ADCI 和 LBCI 患者(17 名 MCI 和 37 名痴呆)。我们对神经心理学评分和区域皮质厚度进行了组间比较。我们还使用广义线性模型评估了 ADCI 和 LBCI 的影响。
与对照组相比,单纯 ADCI 组和单纯 LBCI 组患者双侧内嗅/右侧颞前皮质和双侧前内侧颞叶/基底额皮质存在局限性皮质变薄,而混合疾病组患者广泛的联合皮质存在额外的皮质变薄。ADCI 和 LBCI 对区域皮质变薄的独立影响在广泛的联合皮质中重叠,尤其是在双侧颞顶联合区和顶叶皮质。ADCI 和 LBCI 对 Rey-Osterrieth 复杂图形测试的复制项目有独立的损害作用。
同时患有 ADCI 和 LBCI 与广泛的联合皮质的神经退行性变加重有关,两种疾病都导致了视空间功能障碍。