Study Report

Reference
Citation | Pae, 2004 PubMed |
Full Info | Pae, C.U., Yu, H.S., Kim, J.J., Lee, C.U., Lee, S.J., Lee, K.U., Jun, T.Y., Paik, I.H., Serretti, A. and Lee, C. (2004) BanI polymorphism of the cytosolic phospholipase A2 gene and mood disorders in the Korean population. Neuropsychobiology, 49, 185-188.
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Study
Hypothesis or Background |
Membrane phospholipid abnormalities have been proposed to be involved in the pathogenesis of mood disorders, and in signal transduction and neurotransmitter uptake. Cytosolic phospholipase A2 (cPLA2) is not only an essential enzyme in the metabolism of fatty acids but also in signaling process.
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Sample Information | Sixty-two patients with major depressive disorder (MDD), 50 patients with bipolar I disorder (BID) and 117 healthy controls participated in this study. |
Method Detail | Therefore, we examined the association between the BanI polymorphism of the cPLA2 gene and mood disorders. Sixty-two patients with major depressive disorder (MDD), 50 patients with bipolar I disorder (BID) and 117 healthy controls participated in this study. Genotyping was performed by using PCR-based methods. |
Method Keywords | genotyping |
Result | Genotype and allele distributions in MDD patients were significantly different from those of the controls. In particular, the A2 allele was associated with increased risk of MDD development (p = 0.007, odds ratio = 1.827; confidence interval = 1.141-2.927). However, the polymorphism was not different between BID patients and controls in genotype and allele distribution. |
Conclusions | This preliminary study indicates the need for further studies on the potential role of the cPLA2 gene polymorphism in the susceptibility to mood disorders. |

Relationships reported by
Pae, 2004
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)) |
MDD
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syndrome |
KAT5 (Cytosolic phospholipase A2 (cPLA2)) |
gene |
P-value = 0.007, odds ratio = 1.827; confidence interval = 1.141-2.927 |
Genotype and allele distributions in MDD patients were significantly different from those of the controls. In particular, the A2 allele was associated with increased risk of MDD development (p = 0.007, odds ratio = 1.827; confidence interval = 1.141-2.927) |
Positive
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