BDNF G196A (Val66Met) polymorphism associated with cognitive impairment in Parkinson's disease

被引:42
作者
Bialecka, Monika [1 ]
Kurzawski, Mateusz [1 ]
Roszmann, Anna [2 ,3 ]
Robowski, Piotr [2 ,3 ]
Sitek, Emilia J. [2 ,3 ]
Honczarenko, Krystyna [4 ]
Mak, Monika [5 ]
Deptula-Jarosz, Monika [6 ]
Golab-Janowska, Monika [4 ]
Drozdzik, Marek [1 ]
Slawek, Jarostaw [2 ,3 ]
机构
[1] Pomeranian Med Univ, Dept Expt & Clin Pharmacol, PL-70111 Szczecin, Poland
[2] Med Univ Gdansk, Dept Neurol Psychiat Nursing, PL-80462 Gdansk, Poland
[3] St Adalbert Hosp, Dept Neurol, PL-80462 Gdansk, Poland
[4] Pomeranian Med Univ, Neurol Clin, PL-71251 Szczecin, Poland
[5] Pomeranian Med Univ, Psychiat Clin, PL-71460 Szczecin, Poland
[6] Marie Curie Reg Hosp, Dept Neurol, PL-71455 Szczecin, Poland
关键词
Parkinson's disease; Dementia; Genetic polymorphism; BDNF; NEUROTROPHIC FACTOR GENE; NEURODEGENERATIVE DISEASES; ALZHEIMERS-DISEASE; DEMENTIA; ONSET; AGE; PROGRESSION; POPULATION; DEPRESSION; DISORDERS;
D O I
10.1016/j.neulet.2013.12.051
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 Taq-Man 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. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:86 / 90
页数:5
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