Polymorphism of NACP-Rep1 in Parkinson's disease : An etiologic link with essential tremor?
Identifieur interne : 001915 ( Main/Exploration ); précédent : 001914; suivant : 001916Polymorphism of NACP-Rep1 in Parkinson's disease : An etiologic link with essential tremor?
Auteurs : E Tan [États-Unis] ; T Matsuura [États-Unis] ; S Nagamitsu [États-Unis] ; M Khajavi [États-Unis] ; J Jankovic [États-Unis] ; T Ashizawa [États-Unis]Source :
- Neurology [ 0028-3878 ] ; 2000.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Age of Onset, Aged, Aged, 80 and over, Alleles, Essential Tremor (complications), Essential Tremor (genetics), Exploration, Female, Genotype, Human, Humans, Male, Middle Aged, Nerve Tissue Proteins (genetics), Parkinson Disease (complications), Parkinson Disease (genetics), Parkinson disease, Polymorphism, Polymorphism, Genetic (genetics), Synucleins.
- MESH :
- chemical , genetics : Nerve Tissue Proteins.
- complications : Essential Tremor, Parkinson Disease.
- genetics : Essential Tremor, Parkinson Disease, Polymorphism, Genetic.
- Adult, Age of Onset, Aged, Aged, 80 and over, Alleles, Female, Genotype, Humans, Male, Middle Aged, Synucleins.
Abstract
An allele (263bp) of the nonamyloid component of plaques (NACP)-Repl polymorphism has shown association with sporadic PD in a German population. The authors studied this polymorphism in 100 American PD patients and 100 healthy controls. The authors also studied 46 essential tremor (ET) and 55 Huntington's disease (HD) patients. Allele 263bp was significantly higher in PD patients (OR = 3.86) and ET patients (OR = 6.42) but not HD patients, compared with healthy controls. The association of allele 263bp with PD and ET suggests a possible etiologic link between these two conditions.
Affiliations:
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Le document en format XML
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<term>Essential Tremor (genetics)</term>
<term>Exploration</term>
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<term>Genotype</term>
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<term>Aged, 80 and over</term>
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<front><div type="abstract" xml:lang="en">An allele (263bp) of the nonamyloid component of plaques (NACP)-Repl polymorphism has shown association with sporadic PD in a German population. The authors studied this polymorphism in 100 American PD patients and 100 healthy controls. The authors also studied 46 essential tremor (ET) and 55 Huntington's disease (HD) patients. Allele 263bp was significantly higher in PD patients (OR = 3.86) and ET patients (OR = 6.42) but not HD patients, compared with healthy controls. The association of allele 263bp with PD and ET suggests a possible etiologic link between these two conditions.</div>
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<name sortKey="Ashizawa, T" sort="Ashizawa, T" uniqKey="Ashizawa T" first="T" last="Ashizawa">T Ashizawa</name>
<name sortKey="Ashizawa, T" sort="Ashizawa, T" uniqKey="Ashizawa T" first="T" last="Ashizawa">T Ashizawa</name>
<name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J Jankovic</name>
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<name sortKey="Khajavi, M" sort="Khajavi, M" uniqKey="Khajavi M" first="M" last="Khajavi">M Khajavi</name>
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<name sortKey="Matsuura, T" sort="Matsuura, T" uniqKey="Matsuura T" first="T" last="Matsuura">T Matsuura</name>
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