Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Chen, Shihaoa | Huang, Wentinga | He, Taoa | Zhang, Mulana | Jin, Xinga | Jiang, Lelinb | Xu, Huiqina; * | Chen, Keyangc; *
Affiliations: [a] Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China | [b] Wenzhou Medical University, Wenzhou, China | [c] Department of Neurology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China
Correspondence: [*] Correspondence to: Huiqin Xu, Prof, Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Shangcai Village, Baixiang Street, Ouhai District, Wenzhou City, Zhejiang Province, China. Tel.: +86 13858806368; E-mail: [email protected] and Keyang Chen MD, PhD, Department of Neurology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China, No. 1111, East Section of Wenzhou Avenue, Longwan District, Wenzhou City, Zhejiang Province, China. E-mail: [email protected].
Abstract: Background:Brain-derived neurotrophic factor (BDNF) is a protein synthesized in the brain and widely expressed in the nervous system. Previous studies have demonstrated a controversial role of BDNF in neurological diseases. Objective:In this study, we aimed to assess the association between BDNF levels and the risk of neurological diseases by Mendelian randomization analysis. Methods:From a genome-wide association analysis of plasma proteins comprising 3,301 European participants, we isolated 25 genetic variations as instrumental variables for BDNF levels. Summary statistics data on six common neurological diseases as outcome variables. Two-sample Mendelian randomization (MR) analysis was used to assess whether plasma BDNF is causally related to neurological diseases. We also performed sensitivity analysis to ensure the robustness of the results and reverse MR to exclude potential reverse causality. Results:We confirmed the significant causal relationship between BDNF levels and the risk of Alzheimer’s disease (AD) (OR, 0.92; 95% CI, 0.85, 0.98; p = 0.013). Other methods have also shown similar results. We infer that BDNF also reduces the risk of epilepsy (OR, 0.94; 95% CI, 0.90, 0.98; p = 0.004). In reverse MR analysis, we also found that AD can affect the level of BDNF. Conclusions:Our study suggests higher plasma BDNF was associated with the reduced risk of AD. Moreover, higher plasma BDNF is a protective factor on AD and focal epilepsy. The results provide credence to the idea that BDNF may play a significant role in the development of focal epilepsy and AD.
Keywords: Alzheimer’s disease, brain-derived neurotrophic factor, epilepsy, genome-wide association studies, Mendelian randomization
DOI: 10.3233/JAD-230693
Journal: Journal of Alzheimer's Disease, vol. 96, no. 1, pp. 135-148, 2023
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]