Back to Search Start Over

Genetics of emergent suicidality during antidepressive treatment—Data from a naturalistic study on a large sample of inpatients with a major depressive episode.

Authors :
Musil, Richard
Zill, Peter
Seemüller, Florian
Bondy, Brigitta
Meyer, Sebastian
Spellmann, Ilja
Bender, Wolfram
Adli, Mazda
Heuser, Isabella
Fisher, Robert
Gaebel, Wolfgang
Maier, Wolfgang
Rietschel, Marcella
Rujescu, Dan
Schennach, Rebecca
Möller, Hans-Jürgen
Riedel, Michael
Source :
European Neuropsychopharmacology. Jul2013, Vol. 23 Issue 7, p663-674. 12p.
Publication Year :
2013

Abstract

Abstract: Factors contributing to treatment-emergent suicidal ideation (TESI) using antidepressants have been in the focus of recent research strategies. We investigated previously established clinical predictors of TESI and combined these with several polymorphisms of candidate genes in patients with major depressive disorder. Common polymorphisms involved in the tryptophan hydroxylase 1 (TPH1) and 2 (TPH2), serotonin transporter, monoamine oxidase A (MAOA) and brain-derived neurotrophic factor (BDNF) were investigated in a naturalistic inpatient study of the German research network on depression. We compared patients showing TESI with non-TESI suicidal patients and with non-suicidal patients using univariate tests to detect relevant factors, which were further tested in logistic regression and CART (Classification and Regression Trees) analyses. Of the 269 patients, TESI occurred in 22 patients (17 female), 117 patients were defined as non-TESI suicidal patients, and 130 patients were classified as non-suicidal. When comparing cases with both control groups we found the TPH2 rs1386494 (C/T) polymorphism to be moderately associated with TESI (Univariate tests: TESI vs. non-suicidality: p=0.005; adjusted: p=0.09; TESI vs. non-TESI suicidal patients: p=0.0024; adjusted: p=0.086). This polymorphism remained the only significant genetic factor in addition to clinical predictors in logistic regression and CART analyses. CART analyses suggested interactions with several clinical predictors. Haplotype analyses further supported a contribution of this polymorphism in TESI. The TPH2 rs1386494 (C/T) polymorphism might contribute to the genetic background of TESI. This polymorphism has been previously associated with committed suicide and major depressive disorder. The small number of cases warrants replication in larger patient samples. Lack of a placebo control group hampers definite conclusions on an association with antidepressive treatment. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
0924977X
Volume :
23
Issue :
7
Database :
Academic Search Index
Journal :
European Neuropsychopharmacology
Publication Type :
Academic Journal
Accession number :
89112383
Full Text :
https://doi.org/10.1016/j.euroneuro.2012.08.009