Source:http://linkedlifedata.com/resource/pubmed/id/19500679
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2009-8-11
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pubmed:abstractText |
Levels of extra-synaptic dopamine in the brain vary as a function of polymorphisms at the val158met locus of the catechol-O-methyltransferase (COMT) gene. In vivo studies of this polymorphism in the human brain have typically measured patterns of neural activation during dopamine-mediated tasks in adults. This study is the first to investigate the effects of COMT on brain physiology during rest and in children. We used flow-sensitive arterial spin-labeling (ASL) magnetic resonance imaging to examine brain blood flow (CBF) in 42 children. Compared with val-allele carriers, met-allele homozygotes exhibited greater CBF in mesolimbic, mesocortical, and nigrostriatal dopamine (DA) pathways. Higher CBF in DA-rich brain structures reflects COMT-related baseline differences that (1) underlie the selective behavioral advantages associated with each genotype; (2) affect interpretations of previously reported genotype differences in BOLD signal changes; and (3) serve as a foundation for future studies on the effects of COMT on brain development.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/F32 MH081583-02,
http://linkedlifedata.com/resource/pubmed/grant/MH074849,
http://linkedlifedata.com/resource/pubmed/grant/MH081583,
http://linkedlifedata.com/resource/pubmed/grant/P41 RR009784-09,
http://linkedlifedata.com/resource/pubmed/grant/R01 MH074849-04,
http://linkedlifedata.com/resource/pubmed/grant/RR09784
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1095-9572
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
15
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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 |
217-22
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pubmed:dateRevised |
2011-9-26
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pubmed:meshHeading |
pubmed-meshheading:19500679-Adolescent,
pubmed-meshheading:19500679-Analysis of Variance,
pubmed-meshheading:19500679-Brain,
pubmed-meshheading:19500679-Catechol O-Methyltransferase,
pubmed-meshheading:19500679-Cerebrovascular Circulation,
pubmed-meshheading:19500679-Child,
pubmed-meshheading:19500679-Female,
pubmed-meshheading:19500679-Genotype,
pubmed-meshheading:19500679-Humans,
pubmed-meshheading:19500679-Magnetic Resonance Imaging,
pubmed-meshheading:19500679-Male,
pubmed-meshheading:19500679-Perfusion Imaging,
pubmed-meshheading:19500679-Polymorphism, Genetic,
pubmed-meshheading:19500679-Regional Blood Flow,
pubmed-meshheading:19500679-Rest,
pubmed-meshheading:19500679-Sequence Analysis, DNA
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pubmed:year |
2009
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pubmed:articleTitle |
COMT genotype and resting brain perfusion in children.
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pubmed:affiliation |
Department of Psychology, Stanford University, Stanford, CA 94305-2130, USA. moriah@stanford.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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