Department of Experimental and Clinical Pharmacology, Pomeranian Medical University, Powstańców Wlkp 72, 70-111 Szczecin, Poland.
Department of Neurological-Psychiatric Nursing, Medical University of Gdańsk, Al. Jana Pawła II 50, 80-462, Poland; Department of Neurology, St. Adalbert Hospital, Al. Jana Pawła II 50, 80-462 Gdańsk, Poland.
Neurosci Lett. 2014 Feb 21;561:86-90. doi: 10.1016/j.neulet.2013.12.051. Epub 2014 Jan 3.
Brain-derived neurotrophic factor (BDNF) is a neurotrophin widely expressed in the mammalian brain, regulating neuronal survival and known to influence dopaminergic neurons and cognitive processes. The present study investigated the BDNF Val66Met polymorphism associations with PD risk, and cognitive impairment in PD. A total of 486 study subjects (244 PD and 242 age and sex matched controls) were included in the study. UPDRS score, Hoehn-Yahr staging and the Schwab-England scale were used to assess motor abilities and activity during daily life. The patients were classified into groups with dementia (PDD, n=69) and without it (nPDD, n=166) on the basis of neuropsychological assessment. The most common functional polymorphism in BDNF Val66Met (rs6265, G196A) gene was determined using TaqMan real-time PCR assay. Frequencies of evaluated BDNF alleles and genotypes were similar in PD and the controls. The mean age of disease onset among BDNF Met/Met carriers was later (65.00±6.13) in comparison to Val/Val (57.45±10.68) and Val/Met (56.33±10.91) subjects (p=0.077). The studied BDNF polymorphism was not associated with cognitive status in PD patients. However, patients with Met/Met alleles demonstrated better delayed recall of information than patients with Val/Val alleles. The results of multivariate logistic regression analysis revealed age (p=0.0003) and the disease stage (p=0.002) as independent risk factors predisposing to PD dementia.
脑源性神经营养因子(BDNF)是一种广泛表达于哺乳动物大脑中的神经营养因子,调节神经元存活,并已知影响多巴胺能神经元和认知过程。本研究探讨了 BDNF Val66Met 多态性与 PD 风险和 PD 认知障碍的关系。共有 486 名研究对象(244 名 PD 和 242 名年龄和性别匹配的对照)纳入本研究。使用 UPDRS 评分、Hoehn-Yahr 分期和 Schwab-England 量表评估运动能力和日常生活中的活动。根据神经心理学评估,将患者分为痴呆组(PDD,n=69)和非痴呆组(nPDD,n=166)。使用 TaqMan 实时 PCR 测定 BDNF Val66Met(rs6265,G196A)基因中最常见的功能多态性。PD 和对照组中评估的 BDNF 等位基因和基因型频率相似。BDNF Met/Met 携带者的疾病发病平均年龄较晚(65.00±6.13),而 Val/Val(57.45±10.68)和 Val/Met(56.33±10.91)受试者则更早(p=0.077)。研究的 BDNF 多态性与 PD 患者的认知状态无关。然而,携带 Met/Met 等位基因的患者比携带 Val/Val 等位基因的患者信息延迟回忆更好。多变量逻辑回归分析的结果显示,年龄(p=0.0003)和疾病分期(p=0.002)是导致 PD 痴呆的独立危险因素。