Three polymorphisms of the eNOS gene and plasma levels of metabolites of nitric oxide in depressed Japanese patients: a preliminary report.

Saved in:
Bibliographic Details
Title: Three polymorphisms of the eNOS gene and plasma levels of metabolites of nitric oxide in depressed Japanese patients: a preliminary report.
Authors: Ikenouchi-Sugita, Atsuko, Yoshimura, Reiji, Kishi, Taro, Umene-Nakano, Wakako, Hori, Hikaru, Hayashi, Kenji, Katsuki, Asuka, Ueda, Nobuhisa, Iwata, Nakao, Nakamura, Jun
Source: Human Psychopharmacology: Clinical & Experimental. Oct2011, Vol. 26 Issue 7, p531-534. 4p.
Subjects: Genetic polymorphisms, Mental depression, Coronary disease, Nitric oxide, Blood plasma
Abstract: Background Depression is a risk factor for coronary heart disease. Nitric oxide (NO) plays an important role in both coronary heart disease and depression. Methods Fifty-one inpatients and outpatients who met the Diagnostic and Statistical Manual of Mental Disorders-Fourth Edition criteria for major depressive disorder (MDD) in the university hospital of the University of Occupational and Environmental Health and 58 age-matched and sex-matched healthy controls enrolled in this study. We investigated the association between the three polymorphisms of the endothelial nitric oxide synthase (eNOS) gene (single-nucleotide polymorphism (SNP); rs2070744, rs1799983, variable number tandem repeat (VNTR) in intron 4) and scores on the Hamilton Rating Scale for Depression, plasma metabolites of NO (NOx) or ankle brachial index in patients with MDD and healthy controls. Results We did not find significant differences in the genotype distributions between patients with MDD and healthy volunteers. No associations were observed between any of the polymorphisms of the eNOS gene and the Hamilton Rating Scale for Depression or ankle brachial index in patients with MDD. However, plasma NOx level was significantly associated with a polymorphism of the eNOS gene (rs207044 and variable number tandem repeat in intron 4). Conclusion These results suggest that the direct association was not observed between the polymorphisms of the eNOS gene and the pathogenesis of depression. Copyright © 2011 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]
Copyright of Human Psychopharmacology: Clinical & Experimental is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Psychology and Behavioral Sciences Collection
Description
Abstract:Background Depression is a risk factor for coronary heart disease. Nitric oxide (NO) plays an important role in both coronary heart disease and depression. Methods Fifty-one inpatients and outpatients who met the Diagnostic and Statistical Manual of Mental Disorders-Fourth Edition criteria for major depressive disorder (MDD) in the university hospital of the University of Occupational and Environmental Health and 58 age-matched and sex-matched healthy controls enrolled in this study. We investigated the association between the three polymorphisms of the endothelial nitric oxide synthase (eNOS) gene (single-nucleotide polymorphism (SNP); rs2070744, rs1799983, variable number tandem repeat (VNTR) in intron 4) and scores on the Hamilton Rating Scale for Depression, plasma metabolites of NO (NOx) or ankle brachial index in patients with MDD and healthy controls. Results We did not find significant differences in the genotype distributions between patients with MDD and healthy volunteers. No associations were observed between any of the polymorphisms of the eNOS gene and the Hamilton Rating Scale for Depression or ankle brachial index in patients with MDD. However, plasma NOx level was significantly associated with a polymorphism of the eNOS gene (rs207044 and variable number tandem repeat in intron 4). Conclusion These results suggest that the direct association was not observed between the polymorphisms of the eNOS gene and the pathogenesis of depression. Copyright © 2011 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]
ISSN:08856222
DOI:10.1002/hup.1239