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  4. Mendelian randomization reveals association between retinal thickness and non-motor symptoms of Parkinson's disease
 
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Mendelian randomization reveals association between retinal thickness and non-motor symptoms of Parkinson's disease

Journal
NPJ Parkinson's disease
Journal Volume
9
Journal Issue
1
Pages
163
Date Issued
2023-12-13
Author(s)
Zhou, Hang
Shen, Bibiao
Huang, Zifeng
Zhu, Shuzhen
Yang, Wanlin
Xie, Fen
Luo, Yuqi
Yuan, Feilan
Zhu, Zhaohua
Deng, Chao
Zheng, Wenhua
Yang, Chengwu
CHIN-HSIEN LIN  
Xiao, Bin
Tan, Eng-King
Wang, Qing
DOI
10.1038/s41531-023-00611-z
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/639049
URL
https://api.elsevier.com/content/abstract/scopus_id/85179884521
Abstract
Retinal thickness is related to Parkinson's disease (PD), but its association with the severity of PD is still unclear. We conducted a Mendelian randomized (MR) study to explore the association between retinal thickness and PD. For the two-sample MR analysis, the summary statistics obtained from genome-wide association studies on the thickness of Retinal nerve fiber layer (RNFL) and ganglion cell inner plexiform layer (GCIPL) were employed as exposure, while the summary statistics associated with PD were used as the outcome. The primary approach utilized was inverse variance weighted. To correct for multiple testing, the false discovery rate (FDR) was employed. For sensitivity analysis, an array of robust MR methods was utilized. We found genetically predicted significant association between reduced RNFL thickness and a reduced risk of constipation in PD (odds ratio [OR] = 0.854, 95% confidence interval [CI] (0.782, 0.933), P < 0.001, FDR-corrected P = 0.018). Genetically predicted reduced RNFL thickness was associated with a reduced Unified Parkinson's Disease Rating Scale total score (β = -0.042, 95% CI (-0.079, 0.005), P = 0.025), and reduced GCIPL thickness was associated with a lower risk of constipation (OR = 0.901, 95% CI (0.821, 0.988), P = 0.027) but a higher risk of depression (OR = 1.103, 95% CI (1.016, 1.198), P = 0.020), insomnia (OR = 1.090, 95% CI (1.013, 1.172), P = 0.021), and rapid eye movement sleep behaviour disorder (RBD) (OR = 1.198, 95% CI (1.061, 1.352), P = 0.003). In conclusion, we identify an association between retinal thickness and non-motor symptoms (constipation, depression, insomnia and RBD) in PD, highlighting the potential of retinal thickness as a biomarker for PD nonmotor symptoms.
SDGs

[SDGs]SDG3

Type
journal article

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