痴呆
危险系数
医学
评定量表
累积发病率
老人忧郁量表
内科学
萧条(经济学)
入射(几何)
认知功能衰退
置信区间
帕金森病
疾病
物理疗法
认知
队列
心理学
精神科
抑郁症状
物理
光学
发展心理学
经济
宏观经济学
作者
Victoire Leroy,Ayers Emmeline,Joe Verghese
摘要
Abstract Background Mild parkinsonian signs (MPS) are prevalent in older adults and linked to an increased risk of dementia. However, their association with Motoric Cognitive Risk syndrome (MCR), a pre‐dementia syndrome characterized by slow gait speed and cognitive complaints, is unclear. This study aims to examine the association of MPS with incident MCR. Method Non‐demented older adults without Parkinson’s disease were monitored annually (average follow‐up 30 months). We excluded participants with MCR at baseline and dementia incidence without previous MCR, as non‐cases. MPS were defined at baseline by the presence of bradykinesia, rigidity, or rest tremor rated by a study clinician using the Unified Parkinson’s Disease Rating Scale (UPDRS). MCR was diagnosed using established criteria at baseline and follow‐up. The association of baseline MPS and incident MCR was examined using survival analysis and reported as hazard ratio and 95% confidence intervals (CI). Result Of the 580 participants, 227 (39.1%) had MPS and 44 (7.5%) had MCR at baseline. Of the 513 initially MCR‐free participants, 46 (8.9%) developed incident MCR. Incident MCR cases had a higher prevalence of MPS at baseline compared to participants who did not develop MCR (OR adjusted for age, geriatric depression scale (GDS) score, and stroke history = 3.8, 95% CI 1.8‐8.2), particularly bradykinesia (52.3% vs. 19.0%; p<0.001) and rigidity (54.5% vs. 28.1%; p<0.001). They were older (p<0.001), more disabled (p<0.001), and had more strokes (p = 0.005), and depressive symptoms (p<0.001) compared to individuals who did not develop MCR. Participants with MPS at baseline had a greater risk of developing incident MCR (HR adjusted for age, GDS score, and stroke history = 3.7, 95% CI 1.8‐7.7). Conclusion MPS predicted the onset of MCR, suggesting a significant role in the pathogenesis and in improving early assessment of risk for MCR.
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