Variability and validity of polymorphism association studies in Parkinson's disease.
Identifieur interne : 000261 ( PubMed/Corpus ); précédent : 000260; suivant : 000262Variability and validity of polymorphism association studies in Parkinson's disease.
Auteurs : E Tan ; M. Khajavi ; J Thornby ; S. Nagamitsu ; J. Jankovic ; T. AshizawaSource :
- Neurology [ 0028-3878 ] ; 2000.
English descriptors
- KwdEn :
- Apolipoproteins E (genetics), Arylamine N-Acetyltransferase (genetics), Carrier Proteins (genetics), Case-Control Studies, Catechol O-Methyltransferase (genetics), DNA, Mitochondrial (genetics), Dopamine Plasma Membrane Transport Proteins, Female, Gene Frequency, Genetic Linkage, Genetic Variation (genetics), Glutathione Transferase (genetics), Humans, Isoenzymes (genetics), Male, Membrane Glycoproteins, Membrane Transport Proteins, Monoamine Oxidase (genetics), Nerve Tissue Proteins, Parkinson Disease (genetics), Polymorphism, Genetic (genetics), RNA, Transfer, Glu (genetics), Receptors, Dopamine D2 (genetics), Receptors, Dopamine D4, Reproducibility of Results.
- MESH :
- chemical , genetics : Apolipoproteins E, Arylamine N-Acetyltransferase, Carrier Proteins, Catechol O-Methyltransferase, DNA, Mitochondrial, Glutathione Transferase, Isoenzymes, Monoamine Oxidase, RNA, Transfer, Glu, Receptors, Dopamine D2.
- genetics : Genetic Variation, Parkinson Disease, Polymorphism, Genetic.
- Case-Control Studies, Dopamine Plasma Membrane Transport Proteins, Female, Gene Frequency, Genetic Linkage, Humans, Male, Membrane Glycoproteins, Membrane Transport Proteins, Nerve Tissue Proteins, Receptors, Dopamine D4, Reproducibility of Results.
Abstract
In recent years, interest in gene-environment interactions has spurred a great number of association studies on polymorphism of different genes.
PubMed: 10953187
Links to Exploration step
pubmed:10953187Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Variability and validity of polymorphism association studies in Parkinson's disease.</title><author><name sortKey="Tan, E K" sort="Tan, E K" uniqKey="Tan E" first="E" last="Tan">E Tan</name><affiliation><nlm:affiliation>Department of Neurology, Baylor College of Medicine, Houston, Texas 77030, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Khajavi, M" sort="Khajavi, M" uniqKey="Khajavi M" first="M" last="Khajavi">M. Khajavi</name></author><author><name sortKey="Thornby, J I" sort="Thornby, J I" uniqKey="Thornby J" first="J" last="Thornby">J Thornby</name></author><author><name sortKey="Nagamitsu, S" sort="Nagamitsu, S" uniqKey="Nagamitsu S" first="S" last="Nagamitsu">S. Nagamitsu</name></author><author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J. Jankovic</name></author><author><name sortKey="Ashizawa, T" sort="Ashizawa, T" uniqKey="Ashizawa T" first="T" last="Ashizawa">T. Ashizawa</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2000">2000</date><idno type="RBID">pubmed:10953187</idno><idno type="pmid">10953187</idno><idno type="wicri:Area/PubMed/Corpus">000261</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Variability and validity of polymorphism association studies in Parkinson's disease.</title><author><name sortKey="Tan, E K" sort="Tan, E K" uniqKey="Tan E" first="E" last="Tan">E Tan</name><affiliation><nlm:affiliation>Department of Neurology, Baylor College of Medicine, Houston, Texas 77030, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Khajavi, M" sort="Khajavi, M" uniqKey="Khajavi M" first="M" last="Khajavi">M. Khajavi</name></author><author><name sortKey="Thornby, J I" sort="Thornby, J I" uniqKey="Thornby J" first="J" last="Thornby">J Thornby</name></author><author><name sortKey="Nagamitsu, S" sort="Nagamitsu, S" uniqKey="Nagamitsu S" first="S" last="Nagamitsu">S. Nagamitsu</name></author><author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J. Jankovic</name></author><author><name sortKey="Ashizawa, T" sort="Ashizawa, T" uniqKey="Ashizawa T" first="T" last="Ashizawa">T. Ashizawa</name></author></analytic><series><title level="j">Neurology</title><idno type="ISSN">0028-3878</idno><imprint><date when="2000" type="published">2000</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Apolipoproteins E (genetics)</term><term>Arylamine N-Acetyltransferase (genetics)</term><term>Carrier Proteins (genetics)</term><term>Case-Control Studies</term><term>Catechol O-Methyltransferase (genetics)</term><term>DNA, Mitochondrial (genetics)</term><term>Dopamine Plasma Membrane Transport Proteins</term><term>Female</term><term>Gene Frequency</term><term>Genetic Linkage</term><term>Genetic Variation (genetics)</term><term>Glutathione Transferase (genetics)</term><term>Humans</term><term>Isoenzymes (genetics)</term><term>Male</term><term>Membrane Glycoproteins</term><term>Membrane Transport Proteins</term><term>Monoamine Oxidase (genetics)</term><term>Nerve Tissue Proteins</term><term>Parkinson Disease (genetics)</term><term>Polymorphism, Genetic (genetics)</term><term>RNA, Transfer, Glu (genetics)</term><term>Receptors, Dopamine D2 (genetics)</term><term>Receptors, Dopamine D4</term><term>Reproducibility of Results</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Apolipoproteins E</term><term>Arylamine N-Acetyltransferase</term><term>Carrier Proteins</term><term>Catechol O-Methyltransferase</term><term>DNA, Mitochondrial</term><term>Glutathione Transferase</term><term>Isoenzymes</term><term>Monoamine Oxidase</term><term>RNA, Transfer, Glu</term><term>Receptors, Dopamine D2</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Genetic Variation</term><term>Parkinson Disease</term><term>Polymorphism, Genetic</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Case-Control Studies</term><term>Dopamine Plasma Membrane Transport Proteins</term><term>Female</term><term>Gene Frequency</term><term>Genetic Linkage</term><term>Humans</term><term>Male</term><term>Membrane Glycoproteins</term><term>Membrane Transport Proteins</term><term>Nerve Tissue Proteins</term><term>Receptors, Dopamine D4</term><term>Reproducibility of Results</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In recent years, interest in gene-environment interactions has spurred a great number of association studies on polymorphism of different genes.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">10953187</PMID><DateCreated><Year>2000</Year><Month>08</Month><Day>31</Day></DateCreated><DateCompleted><Year>2000</Year><Month>08</Month><Day>31</Day></DateCompleted><DateRevised><Year>2010</Year><Month>11</Month><Day>18</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0028-3878</ISSN><JournalIssue CitedMedium="Print"><Volume>55</Volume><Issue>4</Issue><PubDate><Year>2000</Year><Month>Aug</Month><Day>22</Day></PubDate></JournalIssue><Title>Neurology</Title><ISOAbbreviation>Neurology</ISOAbbreviation></Journal><ArticleTitle>Variability and validity of polymorphism association studies in Parkinson's disease.</ArticleTitle><Pagination><MedlinePgn>533-8</MedlinePgn></Pagination><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">In recent years, interest in gene-environment interactions has spurred a great number of association studies on polymorphism of different genes.</AbstractText><AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To review case-control studies of genetic polymorphisms in PD, and perform meta-analysis of individual gene polymorphism.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">The authors searched the Medline database (PubMed) for publications (English language) from January 1966 to November 1999 for association studies in PD. The key words used were "PD" and "polymorphism." The authors supplemented the search with relevant references quoted in these published articles. Those with four or more independent studies of a specific gene polymorphism were subjected to meta-analysis, with the exception of cytochrome-P450 enzyme polymorphisms, for which meta-analyses results were already available in the literature.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">The authors identified 84 studies on 14 genes, including dopamine receptors (DRD2 and DRD4), dopamine transporter (DAT), monoamine oxidase (MAOA and MAOB), catechol-O-methyltransferase (COMT), N-acetyltransferase 2 (NAT2), APOE, glutathione transferase (GSTT1, GSTM1, GSTP1, and GSTZ1), and mitochondrial genes (tRNAGlu and ND2). Four polymorphisms showed significant association with PD: slow acetylator genotypes of NAT2 (PD:control OR = 1.36), allele >188bp of the MAOB (GT)n polymorphism (OR = 2.58), the deletion allele of GSTT1 (OR = 1.34), and A4336G of tRNAGlu (OR = 3.0). No significant differences were found for the other genes.</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Significant associations with PD were found in polymorphisms of NAT2, MAOB, GSTT1, and tRNAGlu. Although significant association does not imply a causal relationship between the presence of the polymorphisms and PD pathogenesis, their pathophysiologic significance should be studied further.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Tan</LastName><ForeName>E K</ForeName><Initials>EK</Initials><AffiliationInfo><Affiliation>Department of Neurology, Baylor College of Medicine, Houston, Texas 77030, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Khajavi</LastName><ForeName>M</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Thornby</LastName><ForeName>J I</ForeName><Initials>JI</Initials></Author><Author ValidYN="Y"><LastName>Nagamitsu</LastName><ForeName>S</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Jankovic</LastName><ForeName>J</ForeName><Initials>J</Initials></Author><Author 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protein, human</NameOfSubstance></Chemical><Chemical><RegistryNumber>137750-34-6</RegistryNumber><NameOfSubstance UI="D050638">Receptors, Dopamine D4</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.4.3.4</RegistryNumber><NameOfSubstance UI="D008995">Monoamine Oxidase</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.1.1.6</RegistryNumber><NameOfSubstance UI="D002394">Catechol O-Methyltransferase</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.3.1.5</RegistryNumber><NameOfSubstance UI="D001191">Arylamine N-Acetyltransferase</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.3.1.5</RegistryNumber><NameOfSubstance UI="C478900">NAT2 protein, human</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.5.1.-</RegistryNumber><NameOfSubstance UI="C413545">glutathione S-transferase T1</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.5.1.18</RegistryNumber><NameOfSubstance UI="D005982">Glutathione Transferase</NameOfSubstance></Chemical></ChemicalList><CitationSubset>AIM</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D001057">Apolipoproteins E</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D001191">Arylamine N-Acetyltransferase</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D002352">Carrier Proteins</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D016022">Case-Control Studies</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D002394">Catechol O-Methyltransferase</DescriptorName><QualifierName MajorTopicYN="N" 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UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D007527">Isoenzymes</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="Y" UI="D008562">Membrane Glycoproteins</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="Y" UI="D026901">Membrane Transport Proteins</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008995">Monoamine Oxidase</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="Y" UI="D009419">Nerve Tissue Proteins</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D010300">Parkinson Disease</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D011110">Polymorphism, Genetic</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D012352">RNA, Transfer, Glu</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D017448">Receptors, Dopamine D2</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D050638">Receptors, Dopamine D4</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D015203">Reproducibility of Results</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate 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