Abstract | BACKGROUND: METHODS: In the study we included 514 patients with bipolar disorder and 193 patients with major depressive disorder. Consensus diagnosis by at least two psychiatrists was made, according to DSM-IV (Diagnostic and Statistical Manual of Mental Disorders) criteria, using SCID (Structured Clinical Interview for DSM Disorders). Control group consisted of 732 healthy subjects. Genotyping for eight NR3C1 polymorphisms was done with use of TaqMan SNP (single nucleotide polymorphism) Genotyping Assays. Linkage disequilibrium analysis was done in Haploview. RESULTS: We have found three polymorphisms (rs6198, rs6191 and rs33388) to be associated with major depressive disorder (MDD) and the same polymorphisms were associated with the predominance of depressive symptoms in the course of bipolar disorder. In linkage disequilibrium analysis we observed two haplotype blocks, however, none of those shows involvement in susceptibility to MDD or bipolar disorder. LIMITATIONS: The main limitation of this study is relatively small sample size of MDD patients group. CONCLUSIONS:
|
Authors | Aleksandra Szczepankiewicz, Anna Leszczyńska-Rodziewicz, Joanna Pawlak, Aleksandra Rajewska-Rager, Monika Dmitrzak-Weglarz, Monika Wilkosc, Maria Skibinska, Joanna Hauser |
Journal | Journal of affective disorders
(J Affect Disord)
Vol. 134
Issue 1-3
Pg. 138-44
(Nov 2011)
ISSN: 1573-2517 [Electronic] Netherlands |
PMID | 21764460
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright © 2011 Elsevier B.V. All rights reserved. |
Chemical References |
- NR3C1 protein, human
- Receptors, Glucocorticoid
|
Topics |
- Adult
- Alleles
- Bipolar Disorder
(diagnosis, genetics)
- Case-Control Studies
- Depression
(genetics)
- Depressive Disorder
(diagnosis, genetics)
- Depressive Disorder, Major
(genetics)
- Diagnostic and Statistical Manual of Mental Disorders
- Female
- Genetic Predisposition to Disease
- Genotype
- Haplotypes
- Humans
- Hypothalamo-Hypophyseal System
- Linkage Disequilibrium
- Male
- Middle Aged
- Pituitary-Adrenal System
- Polymorphism, Genetic
- Polymorphism, Single Nucleotide
- Prognosis
- Receptors, Glucocorticoid
(genetics)
|