Possible role of glial cell line-derived neurotrophic factor for predicting cognitive impairment in Parkinson's disease: a case-control study

被引:11
|
作者
Shi, Ming-Yu [1 ,2 ]
Ma, Cheng-Cheng [3 ]
Chen, Fang-Fang [4 ]
Zhou, Xiao-Yu [1 ]
Li, Xue [5 ]
Tang, Chuan-Xi [3 ]
Zhang, Lin [3 ]
Gao, Dian-Shuai [3 ]
机构
[1] Xuzhou Med Univ, Dept Neurol, Affiliated Hosp, Xuzhou, Jiangsu, Peoples R China
[2] First Peoples Hosp Yancheng, Dept Neurol, Yancheng, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Dept Neurobiol & Anat, Xuzhou Key Lab Neurobiol, Xuzhou, Jiangsu, Peoples R China
[4] Suqian First Peoples Hosp, Dept Neurol, Suqian, Jiangsu, Peoples R China
[5] Xuzhou Med Univ, Dept Operating Room, Affiliated Hosp, Xuzhou, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
biomarkers; cognition; factors; GDNF; neurodegenerative diseases; neurons; Parkinson's disease; risk factors; SUBSTANTIA-NIGRA NEURONS; DOPAMINERGIC-NEURONS; DIAGNOSTIC-CRITERIA; MICE MODEL; GDNF; EXPRESSION; DECLINE; DEMENTIA; LEWY;
D O I
10.4103/1673-5374.297091
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glial cell line-derived neurotrophic factor (GDNF) plays an important role in the protection of dopaminergic neurons, but there are few reports of the relationship between GDNF and its precursors (alpha-pro-GDNF and beta-pro-GDNF) and cognitive impairment in Parkinson's disease. This study aimed to investigate the relationship between the serum levels of GDNF and its precursors and cognitive impairment in Parkinson's disease, and to assess their potential as a diagnostic marker. Fifty-three primary outpatients and hospitalized patients with Parkinson's disease (23 men and 30 women) with an average age of 66.58 years were enrolled from the Affiliated Hospital of Xuzhou Medical University of China in this case-control study. The patients were divided into the Parkinson's disease with cognitive impairment group (n = 27) and the Parkinson's disease with normal cognitive function group (n = 26) based on their Mini-Mental State Examination, Montreal Cognitive Assessment, and Clinical Dementia Rating scores. In addition, 26 age- and sex-matched healthy subjects were included as the healthy control group. Results demonstrated that serum GDNF levels were significantly higher in the Parkinson's disease with normal cognitive function group than in the other two groups. There were no significant differences in GDNF precursor levels among the three groups. Correlation analysis revealed that serum GDNF levels, GDNF/alpha-pro-GDNF ratios, and GDNF/beta-pro-GDNF ratios were moderately or highly correlated with the Mini-Mental State Examination, Montreal Cognitive Assessment, and Clinical Dementia Rating scores. To explore the risk factors for cognitive impairment in patients with Parkinson's disease, logistic regression analysis and stepwise linear regression analysis were performed. Both GDNF levels and Hoehn-Yahr stage were risk factors for cognitive impairment in Parkinson's disease, and were the common influencing factors for cognitive scale scores. Neither alpha-pro-GDNF nor beta-pro-GDNF was risk factors for cognitive impairment in Parkinson's disease. A receiver operating characteristic curve of GDNF was generated to predict cognitive function in Parkinson's disease (area under the curve = 0.859). This result indicates that the possibility that serum GDNF can correctly distinguish whether patients with Parkinson's disease have cognitive impairment is 0.859. Together, these results suggest that serum GDNF may be an effective diagnostic marker for cognitive impairment in Parkinson's disease. However, alpha-pro-GDNF and beta-pro-GDNF are not useful for predicting cognitive impairment in this disease. This study was approved by Ethics Committee of the Affiliated Hospital of Xuzhou Medical University, China (approval No. XYFY2017-KL047-01) on November 30, 2017.
引用
收藏
页码:885 / 892
页数:8
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