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Co-occurrence of parkinson disease and multiple sclerosis - a critical note
1Institute of Clinical Neurobiology, Alberichgasse 5/13, Vienna, A-1150, Austria. kurt.jellinger@univie.ac.at.
Abstract:
While multiple sclerosis (MS) is associated with various movement disorders, in particular tremor and ataxia, its combination with parkinsonism is rare and co-occurrence of MS and Parkinson disease (PD) has been reported in only few definite cases. Theories about this co-occurrence range from coincidental to causal, but the true prevalence, basic features and causal relations between the two entities have not been systemically evaluated. Although there are cases of causal relationship between parkinsonism and MS related to demyelinating lesions affecting the dopaminergic nigrostriatal pathway, in a limited number of cases, PD (some gene-mediated) and MS may coexist as two separate diseases in the same patients. The prevalence of MS in LRRK2 PD, while rare, supports an important role for immune function in both disorders, while the role of PD-related PINK is still open. Furthermore, several common genes such as BACE2, CD69, CLC, CPA3 and DEFAs may play important roles in MS and PD, while MS and PD share iron accumulation in substantia nigra, which may be due to protein-protein interaction networks related to metal homeostasis. In view of the various pathogenic possibilities, the causal relationship of concurring MS and PD deserves critical consideration.
Insights
The rare co-occurrence of multiple sclerosis (MS) and Parkinson disease (PD) is explored, examining potential causal links and shared genetic factors. Further research is needed to understand the complex relationship between these two neurological disorders.
Area of Science:
- Neurology
- Neuroimmunology
- Genetics
Background:
- Multiple sclerosis (MS) commonly presents with movement disorders like tremor and ataxia.
- The co-occurrence of MS with parkinsonism, and specifically Parkinson disease (PD), is exceptionally rare.
- Existing theories on MS and PD co-occurrence range from coincidence to causality, lacking systematic evaluation.
Purpose of the Study:
- To investigate the prevalence, characteristics, and causal relationships between MS and PD.
- To explore potential shared genetic and pathogenic mechanisms underlying the co-occurrence of MS and PD.
- To critically assess the evidence for a causal link between demyelinating lesions and parkinsonism.
Main Methods:
- Systematic review of reported cases of MS and PD co-occurrence.
- Analysis of genetic studies investigating shared genes (e.g., LRRK2, PINK1, BACE2, CD69) in MS and PD.
- Examination of pathological findings, including iron accumulation in the substantia nigra.
Main Results:
- While demyelinating lesions can cause parkinsonism in MS, some cases involve PD and MS as distinct coexisting diseases.
- The presence of MS in LRRK2-associated PD suggests a role for immune function in both conditions.
- Shared genetic factors and iron accumulation in the substantia nigra are potential common pathways.
Conclusions:
- The co-occurrence of MS and PD, though rare, warrants critical consideration due to potential shared etiological factors.
- Immune dysregulation and specific genetic predispositions may contribute to both MS and PD.
- Further research is essential to elucidate the complex interplay and causal relationships between these neurological diseases.
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