Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, De Boelelaan 1118, 1081, HZ, Amsterdam, The Netherlands.
Amsterdam Neuroscience, Neurodegeneration, Amsterdam, The Netherlands.
Alzheimers Res Ther. 2022 Sep 15;14(1):132. doi: 10.1186/s13195-022-01075-8.
Quality of life (QoL) is an important outcome from the perspective of patients and their caregivers, in both dementia and pre-dementia stages. Yet, little is known about the long-term changes in QoL over time. We aimed to compare the trajectories of QoL between amyloid-positive and amyloid-negative SCD or MCI patients and to evaluate QoL trajectories along the Alzheimer's disease (AD) continuum of cognitively normal to dementia.
We included longitudinal data of 447 subjective cognitive decline (SCD), 276 mild cognitive impairment (MCI), and 417 AD dementia patients from the Amsterdam Dementia Cohort. We compared QoL trajectories (EQ-5D and visual analog scale (VAS)) between (1) amyloid-positive and amyloid-negative SCD or MCI patients and (2) amyloid-positive SCD, MCI, and dementia patients with linear mixed-effect models. The models were adjusted for age, sex, Charlson Comorbidity Index (CCI), education, and EQ-5D scale (3 or 5 level).
In SCD, amyloid-positive participants had a higher VAS at baseline but showed a steeper decline over time in EQ-5D and VAS than amyloid-negative participants. Also, in MCI, amyloid-positive patients had higher QoL at baseline but subsequently showed a steeper decline in QoL over time compared to amyloid-negative patients. When we compared amyloid-positive patients along the Alzheimer continuum, we found no difference between SCD, MCI, or dementia in baseline QoL, but QoL decreased at a faster rate in the dementia stage compared with the of SCD and MCI stages.
QoL decreased at a faster rate over time in amyloid-positive SCD or MCI patients than amyloid-negative patients. QoL decreases over time along the entire AD continuum of SCD, MCI and dementia, with the strongest decrease in dementia patients. Knowledge of QoL trajectories is essential for the future evaluation of treatments in AD.
生活质量(QoL)是患者及其护理人员的重要关注点,无论是在痴呆症还是痴呆前期阶段。然而,对于 QoL 随时间的长期变化知之甚少。我们旨在比较淀粉样蛋白阳性和淀粉样蛋白阴性 SCD 或 MCI 患者的 QoL 轨迹,并评估沿着认知正常到痴呆的阿尔茨海默病(AD)连续体的 QoL 轨迹。
我们纳入了来自阿姆斯特丹痴呆队列的 447 例主观认知衰退(SCD)、276 例轻度认知障碍(MCI)和 417 例 AD 痴呆症患者的纵向数据。我们使用线性混合效应模型比较了(1)淀粉样蛋白阳性和淀粉样蛋白阴性 SCD 或 MCI 患者以及(2)淀粉样蛋白阳性 SCD、MCI 和痴呆症患者之间的 QoL 轨迹(EQ-5D 和视觉模拟量表(VAS))。模型调整了年龄、性别、Charlson 合并症指数(CCI)、教育程度和 EQ-5D 量表(3 或 5 个水平)。
在 SCD 中,淀粉样蛋白阳性参与者的基线 VAS 较高,但与淀粉样蛋白阴性参与者相比,EQ-5D 和 VAS 的随时间的下降更为陡峭。同样,在 MCI 中,淀粉样蛋白阳性患者的基线 QoL 较高,但随后与淀粉样蛋白阴性患者相比,QoL 随时间的下降更为陡峭。当我们沿着 AD 连续体比较淀粉样蛋白阳性患者时,我们发现 SCD、MCI 或痴呆症的基线 QoL 之间没有差异,但与 SCD 和 MCI 阶段相比,痴呆症阶段的 QoL 下降速度更快。
与淀粉样蛋白阴性患者相比,淀粉样蛋白阳性 SCD 或 MCI 患者的 QoL 随时间的下降速度更快。沿着 SCD、MCI 和痴呆症的整个 AD 连续体,QoL 随时间的推移而下降,痴呆症患者的下降幅度最大。了解 QoL 轨迹对于未来 AD 治疗的评估至关重要。