Journal
MOVEMENT DISORDERS
Volume 24, Issue 11, Pages 1571-1578Publisher
WILEY
DOI: 10.1002/mds.22538
Keywords
parkinsonism; synucleinopathies; Gaucher disease; glucocerebrosidase; risk factor
Categories
Funding
- National Human Genome Research Institute
- National Institutes of Health
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A body of work has emerged over the past decade demonstrating it relationship between mutations in glucocerebrosidase gene (GBA), the gene implicated in Gaucher disease (GD), and the development of parkinsonism. Several different lines of research Support this relationship. First, patients Willi GD who are homozygous for Mutations in GBA have a higher than expected propensity to develop Parkinson's disease (PD). Furthermore, carriers of GBA mutations, particularly family members of patients with GD. have displayed all increased rate of parkinsonism. Subsequently, investigators from centers around the world screened cohorts of patients with parkinsonism for GBA mutations and found that overall, subjects with PD, as well as other Lewy body disorders. have at least a fivefold increase in the number of carriers of GBA Mutations as compared to age-matched controls. In addition. neuropathologic Studies of Subjects with parkinsonism carrying GBA Mutations demonstrate Lewy bodies. depletion of neurons of the substantia nigra, and involvement of hippocampal layers CA2-4. Although the basis for this association has yet to be elucidated, evidence continues to support the role of GBA as a PD risk factor across different centers, synucleinopathies, and ethnicities. Further studies of the association between GD and parkinsonism will stimulate new insights into the pathophysiology of the two disorders and will prove crucial for both genetic counseling of patients and family members and the design of relevant therapeutic strategies for specific patients with parkinsonism. (C) 2009 Movement Disorder Society
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