Source:http://linkedlifedata.com/resource/pubmed/id/14673217
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
2003-12-15
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| pubmed:abstractText |
Catechol-O-methyltransferase (COMT) is an enzyme that inactivates catecholamines, including levodopa. An amino acid change (Val-108-Met) in the COMT protein has been found to result in a change from high to low enzyme activity. In the present study, we genotyped 121 Japanese patients with Parkinson's disease (PD) and 100 controls. Comparison of the allele frequencies revealed that homozygosity for the low-activity allele was significantly more common among PD patients than the controls (p = 0.047, odds ratio = 3.23). In addition, homozygosity for the low-activity allele was overrepresented in PD patients that exhibited the 'wearing-off' phenomenon (p = 0.045, odds ratio = 3.82) or dyskinesia (p = 0.030, odds ratio = 4.80) compared with controls, although these differences were not significant after Bonferroni's correction. Our results may help understand the mechanism that cause complications of levodopa therapy in PD patients.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:issn |
0302-282X
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| pubmed:author | |
| pubmed:copyrightInfo |
Copyright 2003 S. Karger AG, Basel
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| pubmed:issnType |
Print
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| pubmed:volume |
48
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
190-3
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| pubmed:dateRevised |
2006-11-15
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| pubmed:meshHeading |
pubmed-meshheading:14673217-Aged,
pubmed-meshheading:14673217-Catechol O-Methyltransferase,
pubmed-meshheading:14673217-Dyskinesias,
pubmed-meshheading:14673217-Exons,
pubmed-meshheading:14673217-Fatigue Syndrome, Chronic,
pubmed-meshheading:14673217-Female,
pubmed-meshheading:14673217-Genotype,
pubmed-meshheading:14673217-Humans,
pubmed-meshheading:14673217-Male,
pubmed-meshheading:14673217-Methionine,
pubmed-meshheading:14673217-Parkinson Disease,
pubmed-meshheading:14673217-Polymorphism, Genetic,
pubmed-meshheading:14673217-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:14673217-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:14673217-RNA, Messenger,
pubmed-meshheading:14673217-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:14673217-Sequence Analysis, DNA,
pubmed-meshheading:14673217-Valine
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| pubmed:year |
2003
|
| pubmed:articleTitle |
Association between catechol-O-methyltransferase gene polymorphisms and wearing-off and dyskinesia in Parkinson's disease.
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| pubmed:affiliation |
Department of Neurology, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan. masa.wat@igaku.md.tsukuba.ac.jp
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| pubmed:publicationType |
Journal Article,
Comparative Study
|