Center for Neurodegenerative Diseases, University of Salerno, 84131 Salerno, Italy.
J Neurol. 2013 Feb;260(2):438-44. doi: 10.1007/s00415-012-6648-6. Epub 2012 Aug 22.
Epidermal growth factor (EGF) has been proposed as a candidate biomarker for cognitive impairment in Parkinson's disease (PD). We aimed to assess the relationship between serum EGF and cognitive functions in early, drug-naive PD patients and evaluate the predictive value of EGF on cognitive functions in a 2-year follow-up study. Serum EGF was measured in 65 early, drug-naive PD patients, that underwent a comprehensive neuropsychological battery. Motor symptoms were assessed by means of the Unified Parkinson's Disease Rating Scale, Part III (UPDRS-III). Neuropsychological evaluation was repeated after 2 years. Spearman's rank correlation was used to assess the relationship between serum EGF levels and neuropsychological variables. Linear regression analysis was used to evaluate the relationship between EGF and neuropsychological scores as well as other variables (age, gender, UPDRS-III, levodopa equivalent dose, and type of treatment at follow-up) potentially affecting cognitive performance. Variation over time in cognitive scores was analyzed using repeated-measures ANOVA. At baseline, EGF was the only significant variable associated with performance on semantic fluency (R (2) = 0.131; p = 0.005). EGF levels (p = 0.025), together with UPDRS-III (p = 0.009) and age (p = 0.011), were associated with performance on frontal assessment battery (R (2) = 0.260). At 2-year follow-up, EGF was the only significant variable to predict performance on semantic fluency (R (2) = 0.147; p = 0.025) and color naming task of Stroop color-word test (R (2) = 0.121; p = 0.044). Serum EGF levels are related to frontal and temporal cognitive functions in early, drug-naive PD patients and predict performance on frontal and posterior cognitive functions at 2-year follow-up. EGF is proposed as a potential serum biomarker for early cognitive impairment in PD.
表皮生长因子(EGF)被提议作为帕金森病(PD)认知障碍的候选生物标志物。我们旨在评估早期、未经药物治疗的 PD 患者血清 EGF 与认知功能之间的关系,并在 2 年随访研究中评估 EGF 对认知功能的预测价值。测量了 65 名早期、未经药物治疗的 PD 患者的血清 EGF,这些患者接受了全面的神经心理学测试。运动症状采用统一帕金森病评定量表第三部分(UPDRS-III)进行评估。2 年后重复神经心理学评估。采用 Spearman 等级相关分析评估血清 EGF 水平与神经心理学变量之间的关系。采用线性回归分析评估 EGF 与神经心理学评分以及其他可能影响认知表现的变量(年龄、性别、UPDRS-III、左旋多巴等效剂量和随访时的治疗类型)之间的关系。采用重复测量方差分析分析认知评分随时间的变化。在基线时,EGF 是唯一与语义流畅性表现相关的显著变量(R²=0.131;p=0.005)。EGF 水平(p=0.025)、UPDRS-III(p=0.009)和年龄(p=0.011)与 frontal assessment battery 表现相关(R²=0.260)。在 2 年随访时,EGF 是唯一能预测语义流畅性(R²=0.147;p=0.025)和 Stroop 色词测试中颜色命名任务(R²=0.121;p=0.044)表现的显著变量。血清 EGF 水平与早期、未经药物治疗的 PD 患者的额颞叶认知功能有关,并可预测 2 年随访时的额颞叶认知功能。EGF 被提议作为 PD 早期认知障碍的潜在血清生物标志物。