Department of Public Health and Caring Sciences, Geriatrics, Uppsala University, Sweden.
Department of Geriatric and Rehabilitation Medicine, Falu Lasarett, Falun, Sweden.
J Alzheimers Dis. 2019;71(s1):S75-S83. doi: 10.3233/JAD-181265.
Tools to identify individuals at preclinical stages of dementia disorders are needed to enable early interventions. Alterations in dual-task performance have been detected early in progressive neurodegenerative disorders. Hence, dual-task testing may have the potential to screen for cognitive impairment caused by neurodegeneration. Exploring correlations between dual-task performance and biomarkers of neurodegeneration is therefore of interest.
To investigate correlations between Timed Up-and-Go dual-task (TUGdt) outcomes and Alzheimer's disease (AD) cerebrospinal fluid (CSF) biomarkers amyloid-β 42 (Aβ42), total tau (t-tau), and phosphorylated tau (p-tau).
This cross-sectional cohort study included 90 participants (age range 49-84 years) undergoing memory assessment, who were subsequently diagnosed with AD, other dementia disorders, mild cognitive impairment, or subjective cognitive impairment. TUG combined with "Naming Animals" (TUGdt NA) and "Months Backwards" (TUGdt MB), respectively, were used to assess dual-task performance. The number of correct words and time taken to complete the tests were measured. The CSF biomarkers were analysed by ELISA. Spearman's rank correlation was used for analyses between TUGdt outcomes (TUGdt NA and TUGdt MB), and CSF biomarkers, adjusted for age, gender, and educational level.
The number of correct words, as well as the number of correct words/10 s during TUGdt NA correlated negatively to CSF t-tau and p-tau. No correlations were found between any time scores and CSF biomarkers.
The correlations between TUGdt NA and t-tau and p-tau may indicate that neurodegeneration affects dual-task performance. Longitudinal studies are needed to further explore dual-task testing in screening for cognitive impairment due to neurodegeneration.
需要能够识别痴呆症患者临床前阶段的工具,以便进行早期干预。在进行性神经退行性疾病中,已经检测到双重任务表现的改变。因此,双重任务测试可能具有筛查神经退行性病变引起的认知障碍的潜力。因此,探索双重任务表现与神经退行性变生物标志物之间的相关性很有意义。
研究计时起立行走双重任务(TUGdt)结果与阿尔茨海默病(AD)脑脊液(CSF)生物标志物β淀粉样蛋白 42(Aβ42)、总tau(t-tau)和磷酸化 tau(p-tau)之间的相关性。
本横断面队列研究纳入了 90 名(年龄 49-84 岁)接受记忆评估的参与者,随后被诊断为 AD、其他痴呆症、轻度认知障碍或主观认知障碍。分别使用 TUG 联合“命名动物”(TUGdt NA)和“倒数月份”(TUGdt MB)评估双重任务表现。测量完成测试的正确单词数和时间。通过 ELISA 分析 CSF 生物标志物。使用 Spearman 秩相关分析 TUGdt 结果(TUGdt NA 和 TUGdt MB)与 CSF 生物标志物之间的关系,调整年龄、性别和教育水平。
TUGdt NA 的正确单词数以及正确单词/10 秒与 CSF t-tau 和 p-tau 呈负相关。任何时间评分与 CSF 生物标志物之间均无相关性。
TUGdt NA 与 t-tau 和 p-tau 之间的相关性可能表明神经退行性变会影响双重任务表现。需要进行纵向研究,以进一步探索双重任务测试在筛查神经退行性病变引起的认知障碍方面的应用。