| Literature DB >> 20483373 |
Kathrin Reetz1, Vera Tadic, Meike Kasten, Norbert Brüggemann, Alexander Schmidt, Johann Hagenah, Peter P Pramstaller, Alfredo Ramirez, Maria I Behrens, Hartwig R Siebner, Christine Klein, Ferdinand Binkofski.
Abstract
Several genes associated with monogenic forms of Parkinson's disease (PD) have been discovered, opening up new avenues for the investigation of presymptomatic stages of PD. Using voxel-based morphometry in 30 asymptomatic mutation carriers (MC) with mutations in four different genes for PD and 100 healthy controls, we identified an increase in gray matter volume (GMV) in the striatum in asymptomatic Parkin, PINK1, ATP13A2 and, to a much lesser extent, in LRRK2 MC. Moreover, an increase in GMV was found in the parieto-temporo-occipital association cortex in asymptomatic Parkin and ATP13A2 MC. The observed striatal GMV increase might be the common structural correlate of compensatory mechanisms due to the latent dopaminergic deficit, reflecting the different, but probably interrelated pathogenic pathways resulting in nigral cell death. Asymptomatic PINK1 and LRRK2 MC also revealed smaller GMV in the hippocampal region, which might play a role in the observed psychiatric disorders.Entities:
Mesh:
Substances:
Year: 2010 PMID: 20483373 DOI: 10.1016/j.nbd.2010.05.006
Source DB: PubMed Journal: Neurobiol Dis ISSN: 0969-9961 Impact factor: 5.996