Source:http://linkedlifedata.com/resource/pubmed/id/20331984
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2010-5-3
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pubmed:abstractText |
Tryptophan hydroxylase (TPH) is the rate-limiting enzyme in the synthesis of serotonin (5-HT). Genetic variations in human TPH2, a newly identified isoform of TPH, have been shown to impact on enzymatic activity of TPH and to be associated with emotion-related personality traits and mood/anxiety disorders. Identification of an intermediate phenotype that bridges the relationship between genes and behavior may be of great importance in the further clarification of how hTPH2 contributes to emotional regulation. Previous studies have shown that a polymorphism in the upstream regulatory region of hTPH2 (SNP G-703T, rs4570625) correlates functional MRI response of the amygdala. In this study, we examined the effect of this genotype on amygdalar and hippocampal volumes in 208 mentally healthy individuals. To measure volumes of amygdala and hippocampus, gray matter regions of interest were outlined manually on three-dimensional MRI data obtained using a 1.5-T scanner. Additionally, personality traits were evaluated using the Temperament and Character Inventory (TCI). Those subjects with T allele carriers were associated with significantly smaller volumes in bilateral amygdala and hippocampus and higher reward dependence than those with G allele homozygotes. These results suggest that amygdalar and hippocampal volumes assessed using MRI may be a useful intermediate phenotype that will uncover the biological pathway linking 5-HT synthesis and emotional behaviors and affective disorders.
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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 |
May
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pubmed:issn |
1872-6240
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pubmed:author |
pubmed-author:AbeOsamuO,
pubmed-author:AokiShigekiS,
pubmed-author:InoueHideyukiH,
pubmed-author:KasaiKiyotoK,
pubmed-author:RogersMark AMA,
pubmed-author:SasakiTsukasaT,
pubmed-author:SugaMotomuM,
pubmed-author:TakeiKunioK,
pubmed-author:TochigiMamoruM,
pubmed-author:YamadaHaruyasuH,
pubmed-author:YamasueHidenoriH
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pubmed:copyrightInfo |
Copyright 2010 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
17
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pubmed:volume |
1331
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
51-7
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pubmed:meshHeading |
pubmed-meshheading:20331984-Adult,
pubmed-meshheading:20331984-Aged,
pubmed-meshheading:20331984-Amygdala,
pubmed-meshheading:20331984-Female,
pubmed-meshheading:20331984-Genetic Predisposition to Disease,
pubmed-meshheading:20331984-Genotype,
pubmed-meshheading:20331984-Heterozygote,
pubmed-meshheading:20331984-Hippocampus,
pubmed-meshheading:20331984-Humans,
pubmed-meshheading:20331984-Magnetic Resonance Imaging,
pubmed-meshheading:20331984-Male,
pubmed-meshheading:20331984-Middle Aged,
pubmed-meshheading:20331984-Mood Disorders,
pubmed-meshheading:20331984-Personality,
pubmed-meshheading:20331984-Phenotype,
pubmed-meshheading:20331984-Polymorphism, Single Nucleotide,
pubmed-meshheading:20331984-Tryptophan Hydroxylase,
pubmed-meshheading:20331984-Young Adult
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pubmed:year |
2010
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pubmed:articleTitle |
Effect of tryptophan hydroxylase-2 gene variants on amygdalar and hippocampal volumes.
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pubmed:affiliation |
Department of Neuropsychiatry, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan. inouehide-tky@umin.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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