Association of the Tau haplotype with Parkinson's disease in the Greek population
Identifieur interne : 004895 ( Main/Merge ); précédent : 004894; suivant : 004896Association of the Tau haplotype with Parkinson's disease in the Greek population
Auteurs : Liana Fidani [Grèce] ; Kallirhoe Kalinderi [Grèce] ; Sevasti Bostantjopoulou [Grèce] ; Jordi Clarimon [États-Unis] ; Antonis Goulas [Grèce] ; Zoe Katsarou [Grèce] ; John Hardy [États-Unis, Royaume-Uni] ; Alexandros Kotsis [Grèce]Source :
- Movement Disorders [ 0885-3185 ] ; 2006-07.
English descriptors
- KwdEn :
- Aged, Female, Gene Frequency (genetics), Genetics, Population, Genotype, Haplotypes, Humans, Male, Middle Aged, Parkinson Disease (diagnosis), Parkinson Disease (genetics), Parkinson's disease, Polymorphism, Genetic (genetics), Reference Values, Tau, haplotypes, polymorphisms, tau Proteins (genetics).
- MESH :
- chemical , genetics : tau Proteins.
- diagnosis : Parkinson Disease.
- genetics : Gene Frequency, Parkinson Disease, Polymorphism, Genetic.
- Aged, Female, Genetics, Population, Genotype, Haplotypes, Humans, Male, Middle Aged, Reference Values.
Abstract
We compared the distribution of the Tau H1 haplotype and related subhaplotypes in a group of clinically diagnosed Parkinson's disease patients (n = 133) and in control individuals (n = 113) from northern Greece. We were able to detect a statistically significant overrepresentation of the H1H1 genotype in our patient group (OR for H1H1 vs. H1H2 and H2H2: 1.73; 95% CI: 1.03–2.90; P = 0.037). The H1 subhaplotype significantly associated with the disease in our population was different from the one previously reported for a Norwegian population, suggesting that the nature of the association of Tau with Parkinson's disease is influenced by ethnic variation. © 2006 Movement Disorder Society
Url:
DOI: 10.1002/mds.20864
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<front><div type="abstract" xml:lang="en">We compared the distribution of the Tau H1 haplotype and related subhaplotypes in a group of clinically diagnosed Parkinson's disease patients (n = 133) and in control individuals (n = 113) from northern Greece. We were able to detect a statistically significant overrepresentation of the H1H1 genotype in our patient group (OR for H1H1 vs. H1H2 and H2H2: 1.73; 95% CI: 1.03–2.90; P = 0.037). The H1 subhaplotype significantly associated with the disease in our population was different from the one previously reported for a Norwegian population, suggesting that the nature of the association of Tau with Parkinson's disease is influenced by ethnic variation. © 2006 Movement Disorder Society</div>
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<front><div type="abstract" xml:lang="en">We compared the distribution of the Tau H1 haplotype and related subhaplotypes in a group of clinically diagnosed Parkinson's disease patients (n = 133) and in control individuals (n = 113) from northern Greece. We were able to detect a statistically significant overrepresentation of the H1H1 genotype in our patient group (OR for H1H1 vs. H1H2 and H2H2: 1.73; 95% CI: 1.03–2.90; P = 0.037). The H1 subhaplotype significantly associated with the disease in our population was different from the one previously reported for a Norwegian population, suggesting that the nature of the association of Tau with Parkinson's disease is influenced by ethnic variation. © 2006 Movement Disorder Society</div>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Association of the Tau haplotype with Parkinson's disease in the Greek population.</title>
<author><name sortKey="Fidani, Liana" sort="Fidani, Liana" uniqKey="Fidani L" first="Liana" last="Fidani">Liana Fidani</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of General Biology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece. lfidani@med.auth.gr</nlm:affiliation>
<country xml:lang="fr">Grèce</country>
<wicri:regionArea>Department of General Biology, Medical School, Aristotle University of Thessaloniki, Thessaloniki</wicri:regionArea>
<wicri:noRegion>Thessaloniki</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Kalinderi, Kallirhoe" sort="Kalinderi, Kallirhoe" uniqKey="Kalinderi K" first="Kallirhoe" last="Kalinderi">Kallirhoe Kalinderi</name>
</author>
<author><name sortKey="Bostantjopoulou, Sevasti" sort="Bostantjopoulou, Sevasti" uniqKey="Bostantjopoulou S" first="Sevasti" last="Bostantjopoulou">Sevasti Bostantjopoulou</name>
</author>
<author><name sortKey="Clarimon, Jordi" sort="Clarimon, Jordi" uniqKey="Clarimon J" first="Jordi" last="Clarimon">Jordi Clarimon</name>
</author>
<author><name sortKey="Goulas, Antonis" sort="Goulas, Antonis" uniqKey="Goulas A" first="Antonis" last="Goulas">Antonis Goulas</name>
</author>
<author><name sortKey="Katsarou, Zoe" sort="Katsarou, Zoe" uniqKey="Katsarou Z" first="Zoe" last="Katsarou">Zoe Katsarou</name>
</author>
<author><name sortKey="Hardy, John" sort="Hardy, John" uniqKey="Hardy J" first="John" last="Hardy">John Hardy</name>
</author>
<author><name sortKey="Kotsis, Alexandros" sort="Kotsis, Alexandros" uniqKey="Kotsis A" first="Alexandros" last="Kotsis">Alexandros Kotsis</name>
</author>
</analytic>
<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2006" type="published">2006</date>
</imprint>
</series>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Gene Frequency (genetics)</term>
<term>Genetics, Population</term>
<term>Genotype</term>
<term>Haplotypes</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinson Disease (genetics)</term>
<term>Polymorphism, Genetic (genetics)</term>
<term>Reference Values</term>
<term>tau Proteins (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>tau Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Gene Frequency</term>
<term>Parkinson Disease</term>
<term>Polymorphism, Genetic</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Genetics, Population</term>
<term>Genotype</term>
<term>Haplotypes</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Reference Values</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">We compared the distribution of the Tau H1 haplotype and related subhaplotypes in a group of clinically diagnosed Parkinson's disease patients (n = 133) and in control individuals (n = 113) from northern Greece. We were able to detect a statistically significant overrepresentation of the H1H1 genotype in our patient group (OR for H1H1 vs. H1H2 and H2H2: 1.73; 95% CI: 1.03-2.90; P = 0.037). The H1 subhaplotype significantly associated with the disease in our population was different from the one previously reported for a Norwegian population, suggesting that the nature of the association of Tau with Parkinson's disease is influenced by ethnic variation.</div>
</front>
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