Centre for Age-Related Medicine (SESAM), Stavanger University Hospital, Stavanger, Norway.
Semillero de Neurociencias y Envejecimiento, Ageing Institute, Medical School Pontificia Universidad Javeriana, Bogotá, Colombia.
Dement Geriatr Cogn Disord. 2022;51(1):63-72. doi: 10.1159/000522094. Epub 2022 Mar 25.
Early markers of neurodegeneration provide an opportunity to detect, monitor, and initiate interventions in individuals who have an increased risk of developing dementia. Here, we investigated whether the Timed Up and Go (TUG) test is associated with early brain neurodegeneration and whether the TUG test could be a marker of cognitive decline in people with subjective cognitive decline (SCD).
This is a longitudinal analysis of the Dementia Disease Initiation Study, a prospective, community-based, cohort study from Norway, designed to investigate early markers of cognitive impairment and dementia. Participants were classified as SCD and healthy controls (HC). The main studied variables were the TUG test and cognition as measured by the Mini-Mental State Examination and the Consortium to Establish a Registry for Alzheimer's Disease memory composite score. Additionally, we investigated the cross-sectional association of brain morphology with the TUG using 1.5T-MRI.
The sample included 45 participants (SCD = 21, HC = 24) followed during a mean time of 1.50 ± 0.70 years. At baseline, the cognitive performance did not differ between the groups, but TUG was longer in SCD. Slower baseline TUG was associated with a faster cognitive decline in both groups and it was also associated with reduced cortical thickness especially in motor, executive, associative, and somatosensory cortical regions in people with SCD.
DISCUSSION/CONCLUSION: TUG predicted cognitive change in individuals with SCD, and there was a negative association between TUG and cortical thickness. TUG is a promising cheap and noninvasive marker of early cognitive decline and may help initiate interventions in individuals who have an increased risk of dementia.
神经退行性变的早期标志物为检测、监测和启动高危痴呆个体的干预提供了机会。在这里,我们研究了计时起立行走(TUG)测试是否与早期脑神经退行性变有关,以及 TUG 测试是否可以作为主观认知下降(SCD)人群认知能力下降的标志物。
这是挪威开展的痴呆症发病研究(Dementia Disease Initiation Study)的一项纵向分析,该研究是一项前瞻性、基于社区的队列研究,旨在研究认知障碍和痴呆的早期标志物。参与者被分为 SCD 和健康对照组(HC)。主要研究变量是 TUG 测试和认知,认知通过简易精神状态检查和阿尔茨海默病协作研究记忆综合评分来衡量。此外,我们还使用 1.5T-MRI 研究了脑形态与 TUG 的横断面关联。
样本包括 45 名参与者(SCD=21 名,HC=24 名),平均随访时间为 1.50±0.70 年。在基线时,两组的认知表现没有差异,但 SCD 组的 TUG 时间较长。两组中基线 TUG 较慢与认知下降较快相关,并且在 SCD 患者中与皮质厚度减少相关,特别是在运动、执行、联想和躯体感觉皮质区域。
讨论/结论:TUG 预测了 SCD 个体的认知变化,TUG 与皮质厚度呈负相关。TUG 是一种很有前途的廉价、非侵入性的早期认知下降标志物,可能有助于对痴呆风险增加的个体进行干预。