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Aβ42/Aβ40 and Aβ42/Aβ38 Ratios Are Associated with Measures of Gait Variability and Activities of Daily Living in Mild Alzheimer’s Disease: A Pilot Study

机译:Aβ42/Aβ40和Aβ42/Aβ38比率与轻度阿尔茨海默氏病步态变异性和日常生活活动的测量相关:一项初步研究

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摘要

Gait disturbances are some of the earliest changes in dementia and their monitoring presents an opportunity for early diagnosis. The exact relationship between gait and well-established biomarkers of Alzheimer’s disease (AD) remains to be clarified. In this study we compared gait-related measures with cerebrospinal fluid (CSF) markers of AD pathology. We recruited seventeen participants with mild AD in a multi-site study and performed gait assessment as well as lumbar punctures to obtain CSF. CSF Aβ42/Aβ40 and Aβ42/Aβ38 correlated positively with measures of variability (step time and step length) in the clinic-based assessments. This was driven by a negative relationship between gait variability and Aβ40 and Aβ38 but not Aβ42.The amyloid ratios and gait variability measures were also associated with more severe functional impairment. We interpret these data as an indication that increasing amyloid production (i.e., increasing Aβ40 and Aβ38) is associated with diminishing cognitive-motor control of gait. These preliminary results suggest that the two amyloid ratios may be a marker of the earliest disturbances in the interplay between cognitive and motor control which characterize dementia.
机译:步态障碍是痴呆症的最早变化,对其的监测为早期诊断提供了机会。步态与早老性阿尔茨海默氏病(AD)生物标记物之间的确切关系仍有待阐明。在这项研究中,我们将步态相关措施与AD病理的脑脊液(CSF)标记进行了比较。我们在一项多地点研究中招募了17名轻度AD患者,并进行步态评估和腰穿以获取CSF。在基于临床的评估中,CSFAβ42/Aβ40和Aβ42/Aβ38与变异性度量(步长和步长)呈正相关。这是由步态变异性与Aβ40和Aβ38而不是Aβ42呈负相关引起的。淀粉样蛋白比率和步态变异性测定还与更严重的功能障碍相关。我们将这些数据解释为淀粉样蛋白产生增加(即Aβ40和Aβ38增加)与步态的认知运动控制减弱相关的指示。这些初步结果表明,这两种淀粉样蛋白比率可能是认知障碍和运动控制之间相互作用的最早障碍的标志,这是痴呆症的特征。

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