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Published on: April 4, 2018
Myelin-associated oligodendrocyte basic protein rs616147 polymorphism as a risk factor for Parkinson's disease
Vasileios Siokas1, Athina-Maria Aloizou1, Ioannis Liampas1
1Laboratory of Neurogenetics, Department of Neurology, University Hospital of Larissa, Faculty of Medicine, School of Health Sciences, Larissa, Greece.
Background:
The rs616147 polymorphism of the myelin-associated oligodendrocyte basic protein (MOBP) gene locus has been associated with amyotrophic lateral sclerosis (ALS). ALS and Parkinson's disease (PD) are two common neurodegenerative disorders that share features regarding their etiology, pathophysiology, and genetic backgrounds. While the MOBP rs616147 polymorphism has been associated with ALS, little is known about its role in PD.
Objective:
To assess the role of MOBP rs616147 on PD risk.
Methods:
This case-control comparison study consists of 358 PD-affected cases and 358 controls from the Neurology Clinic of the University Hospital of Larissa, University of Thessaly, Faculty of Medicine, in Greece. The diagnosis of PD was made by a specialist neurologist according to the UK Parkinson's Disease Society Brain Bank's clinical criteria. All the participants were genotyped for the MOBP rs616147. Furthermore, in order to validate our results, we genotyped 327 patients with Alzheimer's disease (AD) for MOBP rs616147 and compared them with the control group.
Results:
According to the univariate analysis, there was a significant association between rs616147 and PD in the dominant (OR [95% C.I.] = 0.70 [0.52-0.94], p = .018), the overdominant (OR [95% C.I.] = 0.68 [0.50-0.92], p = .011), and in the codominant (G/A VS G/G; OR [95% C.I.] = 0.66 [0.48-0.91], p = .035) modes of inheritance. In contrast, there was no association between the MOBP rs616147 polymorphism and AD.
Conclusions:
We provide preliminary results associating MOBP rs616147 genetic variant with PD.
Insights
The myelin-associated oligodendrocyte basic protein (MOBP) rs616147 genetic variant is associated with a reduced risk of Parkinson's disease (PD). This finding suggests a potential genetic link between PD and other neurodegenerative disorders like ALS.
Area of Science:
- Neurogenetics
- Neurodegenerative Diseases
- Molecular Biology
Background:
- The rs616147 polymorphism in the myelin-associated oligodendrocyte basic protein (MOBP) gene has been linked to amyotrophic lateral sclerosis (ALS).
- Amyotrophic lateral sclerosis (ALS) and Parkinson's disease (PD) share etiological, pathophysiological, and genetic similarities.
- The role of the MOBP rs616147 polymorphism in Parkinson's disease (PD) risk remains largely unexplored.
Purpose of the Study:
- To investigate the association between the MOBP rs616147 polymorphism and the risk of developing Parkinson's disease (PD).
Main Methods:
- A case-control study was conducted with 358 PD patients and 358 controls from Greece.
- Participants were genotyped for the MOBP rs616147 polymorphism.
- Alzheimer's disease (AD) patients (n=327) were also genotyped for MOBP rs616147 to validate findings against controls.
Main Results:
- Univariate analysis revealed a significant association between the MOBP rs616147 polymorphism and PD risk across dominant, overdominant, and codominant inheritance models.
- Specifically, the rs616147 polymorphism showed a protective effect against PD.
- No significant association was found between the MOBP rs616147 polymorphism and Alzheimer's disease (AD) risk.
Conclusions:
- The study provides preliminary evidence suggesting that the MOBP rs616147 genetic variant is associated with Parkinson's disease (PD).
- This finding may indicate shared genetic factors between PD and other neurodegenerative conditions like ALS.
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