Glucocerebrosidase mutations are an important risk factor for Lewy body disorders

Abstract

The synucleinopathies are neurodegenerative disorders defined by inclusions composed of aberrantly fibrillized α-synuclein, but factors contributing to this process remain largely unknown. The authors examined the glucocerebrosidase gene in 75 autopsy specimens with different synucleinopathies and identified mutations in 23% of cases of dementia with Lewy bodies, expanding on previous findings in subjects with Parkinson disease. Mutations in this lysosomal protein may interfere with the clearance or promote aggregation of α-synuclein.