Department of Pathology, Stanford University School of Medicine, Palo Alto, CA, USA.
Department of Neurology, University of Washington School of Medicine, Seattle, WA, USA.
Parkinsonism Relat Disord. 2018 May;50:29-36. doi: 10.1016/j.parkreldis.2018.02.007. Epub 2018 Feb 9.
Identification of factors associated with progression of cognitive symptoms in Parkinson's disease (PD) is important for treatment planning, clinical care, and design of future clinical trials. The current study sought to identify whether prediction of cognitive progression is aided by examining baseline cognitive features, and whether this differs according to stage of cognitive disease.
Participants with PD in the Pacific Udall Center Clinical Consortium who had longitudinal data available and were nondemented at baseline were included in the study (n = 418). Logistic and Cox regression models were utilized to examine the relationship between cognitive, demographic, and clinical variables with risk and time to progression from no cognitive impairment to mild cognitive impairment (PD-MCI) or dementia (PDD), and from PD-MCI to PDD.
Processing speed (OR = 1.05, p = 0.009) and working memory (OR = 1.01, p = 0.03) were associated with conversion to PDD among those with PD-MCI at baseline, over and above demographic variables. Conversely, the primary predictive factor in the transition from no cognitive impairment to PD-MCI or PDD was male sex (OR = 4.47, p = 0.004), and males progressed more rapidly than females (p = 0.01). Further, among females with shorter disease duration, progression was slower than for their male counterparts, and poor baseline performance on semantic verbal fluency was associated with shorter time to cognitive impairment in females but not in males.
This study provides evidence for sex differences in the progression to cognitive impairment in PD, while specific cognitive features become more important indicators of progression with impending conversion to PDD.
识别与帕金森病(PD)认知症状进展相关的因素对于治疗计划、临床护理和未来临床试验的设计非常重要。本研究旨在确定通过检查基线认知特征是否有助于预测认知进展,以及这是否因认知疾病的阶段而异。
纳入了太平洋乌德尔中心临床联合会中具有纵向数据且基线时无痴呆的 PD 患者(n=418)。利用逻辑回归和 Cox 回归模型,研究了认知、人口统计学和临床变量与无认知障碍进展为轻度认知障碍(PD-MCI)或痴呆(PDD)以及从 PD-MCI 进展为 PDD 的风险和时间之间的关系。
在基线时患有 PD-MCI 的患者中,与向 PDD 转化相关的因素包括处理速度(OR=1.05,p=0.009)和工作记忆(OR=1.01,p=0.03),超过了人口统计学变量。相反,从无认知障碍进展为 PD-MCI 或 PDD 的主要预测因素是男性(OR=4.47,p=0.004),男性的进展速度快于女性(p=0.01)。此外,在疾病持续时间较短的女性中,进展速度比男性慢,而女性的语义流畅性较差与认知障碍的发生时间较短有关,但在男性中则没有。
本研究为 PD 认知障碍进展中的性别差异提供了证据,而特定的认知特征在向 PDD 转化时成为进展的更重要指标。