Source:http://linkedlifedata.com/resource/pubmed/id/11136354
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2001-2-8
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pubmed:abstractText |
Recently, 8-oxo-7,8-dihydrodeoxyguanosine triphosphatase (8-oxo-dGTPase; MTH1), a key enzyme for preventing oxidative stress-induced DNA damage, has been found to be expressed aberrantly in the nigrostriatal dopaminergic neurones in the brains of those with Parkinson's disease (PD). A valine (Val) to methionine (Met) polymorphism at codon 83 in exon 4 of the MTH1 gene was studied in 73 patients with sporadic PD and 151 age-matched non-PD controls by PCR-RFLP analysis, to determine a possible association of this polymorphism with development of PD. The frequency of either 83Val or 83Met allele was not statistically different between PD patients (92.5% or 7.5%) and the controls (88.7% or 11.3%) (chi(2) = 1.511, P = 0.2190). The 83Met/Met homozygotes consisting of an infrequent genotype in the control population (1.3%) were not found in the PD group. The frequency of both 83Val/Met heterozygotes and 83Met/Met homozygotes combined was not statistically different between PD patients (15.1%) and the controls (21.2%), compared with that of the 83Val/Val homozygotes (chi(2) = 1.190, P = 0.2754). These results indicate that the 83Val/Met polymorphism in the MTH1 gene is not associated with an increased risk for development of sporadic PD.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/8-oxodGTPase,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Repair Enzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Methionine,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoric Monoester Hydrolases,
http://linkedlifedata.com/resource/pubmed/chemical/Valine
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1351-5101
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
673-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11136354-Aged,
pubmed-meshheading:11136354-Aged, 80 and over,
pubmed-meshheading:11136354-Amino Acid Substitution,
pubmed-meshheading:11136354-DNA Repair Enzymes,
pubmed-meshheading:11136354-Exons,
pubmed-meshheading:11136354-Female,
pubmed-meshheading:11136354-Humans,
pubmed-meshheading:11136354-Male,
pubmed-meshheading:11136354-Methionine,
pubmed-meshheading:11136354-Middle Aged,
pubmed-meshheading:11136354-Parkinson Disease,
pubmed-meshheading:11136354-Phosphoric Monoester Hydrolases,
pubmed-meshheading:11136354-Polymerase Chain Reaction,
pubmed-meshheading:11136354-Polymorphism, Genetic,
pubmed-meshheading:11136354-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:11136354-Reference Values,
pubmed-meshheading:11136354-Valine
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pubmed:year |
2000
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pubmed:articleTitle |
A valine to methionine polymorphism at codon 83 in the 8-oxo-dGTPase gene MTH1 is not associated with sporadic Parkinson's disease.
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pubmed:affiliation |
Division of Neurology, Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan. satojl@post.saga-med.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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