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Association of GST M1 null polymorphism with Parkinson's disease in a Chilean population with a strong Amerindian genetic component
We have studied the association of a null mutation of Glutathione Transferase M1 (GST M1*0/0) with Parkinson's disease (MIM 168600) in a Chilean population with a strong Amerindian genetic component. We determined the genotype in 349 patients with idiopathic Parkinson's disease (174 female...
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Published in: | Neuroscience letters 2007-05, Vol.418 (2), p.181-185 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We have studied the association of a null mutation of Glutathione Transferase M1 (GST M1*0/0) with Parkinson's disease (MIM 168600) in a Chilean population with a strong Amerindian genetic component. We determined the genotype in 349 patients with idiopathic Parkinson's disease (174 female and 175 male; 66.84
±
10.7 years of age), and compared that to 611 controls (457 female and 254 male; 62
±
13.4 years of age). A significant association of the null mutation in GST M1 with Parkinson's disease was found (
p
=
0.021), and the association was strongest in the earlier age range. An association of GSTM1*0/0 with Parkinson's disease supports the hypothesis that Glutathione Transferase M1 plays a role in protecting astrocytes against toxic dopamine oxidative metabolism, and most likely by preventing toxic one-electron reduction of aminochrome. |
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ISSN: | 0304-3940 1872-7972 |
DOI: | 10.1016/j.neulet.2007.03.024 |