| Literature DB >> 17546678 |
Chiara Balducci1, Laura Pierguidi2,3, Emanuele Persichetti1, Lucilla Parnetti2, Michele Sbaragli1, Carmelo Tassi4, Aldo Orlacchio4, Paolo Calabresi2,3, Tommaso Beccari1, Aroldo Rossi2.
Abstract
Recent studies have shown a genetic association between glucocerebrosidase deficiencies and Parkinson's disease (PD). To further explore this issue the activity of beta-glucocerebrosidase and the activities of other lysosomal enzymes, alpha-mannosidase, beta-mannosidase, beta-hexosaminidase, and beta-galactosidase have been evaluated in the cerebrospinal fluid (CSF) of PD patients. The activities of alpha-mannosidase, beta-mannosidase, beta-glucocerebrosidase, and beta-hexosaminidase were substantially decreased in the CSF of PD patients, while levels of beta-galactosidase were essentially identical to controls. This study indicates that in PD several lysosomal hydrolases have decreased activities, further supporting a possible link between pathophysiological mechanisms underlying PD and lysosomal hydrolases. Copyright 2007 Movement Disorder SocietyEntities:
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Year: 2007 PMID: 17546678 DOI: 10.1002/mds.21399
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338