Persson Karin, Barca Maria Lage, Eldholm Rannveig Sakshaug, Cavallin Lena, Šaltytė Benth Jūratė, Selbæk Geir, Brækhus Anne, Saltvedt Ingvild, Engedal Knut
Norwegian National Advisory Unit on Ageing and Health, Vestfold Hospital Trust, Tønsberg, Norway.
Dement Geriatr Cogn Disord. 2017;44(1-2):12-24. doi: 10.1159/000477342. Epub 2017 Jun 15.
BACKGROUND/AIMS: To evaluate whether visual assessment of medial temporal lobe atrophy (vaMTA) can predict 2-year conversion from mild cognitive impairment (MCI) to dementia and progression of MCI and Alzheimer's disease dementia as measured by the Clinical Dementia Rating Scale Sum of Boxes score (CDR-SB).
vaMTA was performed in 94 patients with MCI according to the Winblad criteria and in 124 patients with AD according to ICD-10 and NINCDS-ADRDA criteria. Demographic data, the Consortium to Establish a Registry for Alzheimer's Disease 10-word delayed recall, APOE ɛ4 status, Cornell Scale for Depression in Dementia, and comorbid hypertension were used as covariates.
vaMTA was associated with MCI conversion in an unadjusted model but not in an adjusted model (p = 0.075), where delayed recall and APOE ɛ4 status were significant predictors. With CDR-SB change as the outcome, an interaction between vaMTA and diagnosis was found, but in the adjusted model only delayed recall and age were significant predictors. For vaMTA below 2, the association between vaMTA and CDR-SB change differed between diagnostic groups. Similar results were found based on a trajectory analysis.
In adjusted models, memory function, APOE ɛ4 status and age were significant predictors of disease progression, not vaMTA. The association between vaMTA and CDR-SB change was different in patients with MCI and Alzheimer's disease dementia.
背景/目的:评估内侧颞叶萎缩的视觉评估(vaMTA)能否预测轻度认知障碍(MCI)在2年内转化为痴呆,以及MCI和阿尔茨海默病痴呆的进展情况,进展情况通过临床痴呆评定量表总盒分(CDR-SB)来衡量。
根据温布拉德标准对94例MCI患者进行vaMTA,根据ICD-10和NINCDS-ADRDA标准对124例阿尔茨海默病(AD)患者进行vaMTA。将人口统计学数据、阿尔茨海默病注册协会10字延迟回忆、APOE ε4状态、痴呆抑郁康奈尔量表以及合并高血压作为协变量。
在未调整模型中,vaMTA与MCI转化相关,但在调整模型中不相关(p = 0.075),其中延迟回忆和APOE ε4状态是显著预测因素。以CDR-SB变化为结果,发现vaMTA与诊断之间存在交互作用,但在调整模型中只有延迟回忆和年龄是显著预测因素。对于vaMTA低于2的情况,vaMTA与CDR-SB变化之间的关联在不同诊断组中有所不同。基于轨迹分析也发现了类似结果。
在调整模型中,记忆功能、APOE ε4状态和年龄是疾病进展的显著预测因素,而非vaMTA。vaMTA与CDR-SB变化之间的关联在MCI患者和阿尔茨海默病痴呆患者中有所不同。