Study Report
Reference
Citation | Lee, 2009 PubMed |
Full Info | Lee, B.T., Lee, H.Y., Lee, B.C., Pae, C.U., Yoon, B.J., Ryu, S.G., Choi, I.G., Lee, M.S. and Ham, B.J. (2009) Impact of the tryptophan hydroxylase 1 gene A218C polymorphism on amygdala activity in response to affective facial stimuli in patients with major depressive disorder. Genes Brain Behav, 8, 512-518.
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Study
Hypothesis or Background |
Tryptophan hydroxylase-1 (TPH1) is the rate-limiting enzyme in serotonin biosynthesis, and allelic variations at the TPH1 locus have been implicated in the pathophysiology of depression.
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Sample Information | 26 right-handed female subjects with major depressive disorder (MDD) |
Method Detail | Using 1.5-Tesla functional magnetic resonance imaging, we investigated the possible relationship between TPH1 A218C polymorphism and amygdala response to negative facial stimuli in 26 right-handed female subjects with major depressive disorder (MDD). Genotyping was performed with the polymerase chain reaction |
Method Keywords | functional magnetic resonance imaging (fMRI); Q-PCR |
Result | We found a significant association between A allele of the TPH1 A218C polymorphism and neural activations in response to negative facial stimuli. Subjects with the A allele of the TPH1 A218C polymorphism showed greater brain activity in the bilateral amygdala under the sad vs. the neutral condition compared with subjects homozygous for the C allele. |
Conclusions | Our results suggest that the A218C polymorphism of the TPH1 gene serves as a modulator of amygdala activity in patients with MDD. |
Relationships reported by
Lee, 2009
Component A Approved Name (Name in Paper) |
Component A Type |
Component B Approved Name (Name in Paper) |
Component B Type |
Statistical Result |
Relationship Description |
Result Category (Positive/Negative)) |
Amygdala (amygdala)
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brain morphology and function |
TPH1 (TPH1) |
gene |
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Subjects with the A allele of the TPH1 A218C polymorphism showed greater brain activity in the bilateral amygdala under the sad vs. the neutral condition compared with subjects homozygous for the C allele. |
Positive
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