Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2009-10-14
pubmed:abstractText
The aim of this study was to investigate genetic predictors of an increase in suicidal ideation during treatment with a selective serotonin reuptake inhibitor or a tricyclic antidepressant. A total of 796 adult patients with major depressive disorder who were treated with a flexible dosage of escitalopram or nortriptyline in Genome-based Therapeutic Drugs for Depression (GENDEP) were included in the sample and provided data on suicidal ideation. Nine candidate genes involved in neurotrophic, serotonergic, and noradrenergic pathways were selected based on previous association studies with suicidal ideation or behavior. Using a logistic regression model, 123 polymorphisms in these genes were compared between subjects with an increase in suicidal ideation and those without any increase in suicidal ideation. Polymorphisms in BDNF, the gene encoding the brain-derived neurotrophic factor, were significantly associated with an increase in suicidal ideation. The strongest association was observed for rs962369 in BDNF (p=0.0015). Moreover, a significant interaction was found between variants in BDNF and NTRK2, the gene encoding the BNDF receptor (p=0.0003). Among men taking nortriptyline, suicidality was also associated with rs11195419 SNP in the alpha(2A)-adrenergic receptor gene (ADRA2A) (p=0.007). The associations observed with polymorphisms in BDNF suggest the involvement of the neurotrophic system in vulnerability to suicidality. Epistasis between BDNF and NTRK2 suggests that genetic variations in the two genes are involved in the same causal mechanisms leading to suicidality during antidepressant treatment. Among men, genetic variation in noradrenergic signaling may interact with norepinephrine reuptake-inhibiting antidepressants, thereby contributing to suicidality.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1740-634X
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2517-28
pubmed:dateRevised
2011-5-18
pubmed:meshHeading
pubmed-meshheading:19641488-Adult, pubmed-meshheading:19641488-Antidepressive Agents, pubmed-meshheading:19641488-Brain-Derived Neurotrophic Factor, pubmed-meshheading:19641488-Citalopram, pubmed-meshheading:19641488-Depressive Disorder, Major, pubmed-meshheading:19641488-Female, pubmed-meshheading:19641488-Follow-Up Studies, pubmed-meshheading:19641488-Genetic Predisposition to Disease, pubmed-meshheading:19641488-Haplotypes, pubmed-meshheading:19641488-Humans, pubmed-meshheading:19641488-Linkage Disequilibrium, pubmed-meshheading:19641488-Logistic Models, pubmed-meshheading:19641488-Male, pubmed-meshheading:19641488-Nortriptyline, pubmed-meshheading:19641488-Polymorphism, Genetic, pubmed-meshheading:19641488-Polymorphism, Single Nucleotide, pubmed-meshheading:19641488-Receptor, trkB, pubmed-meshheading:19641488-Receptors, Adrenergic, alpha-2, pubmed-meshheading:19641488-Sex Factors, pubmed-meshheading:19641488-Suicide
pubmed:year
2009
pubmed:articleTitle
Genetic predictors of increase in suicidal ideation during antidepressant treatment in the GENDEP project.
pubmed:affiliation
MRC Social Genetic and Developmental Psychiatry Center, Institute of Psychiatry, King's College Lodon, London, UK. nader.perroud@iop.kcl.ac.uk
pubmed:publicationType
Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't, Multicenter Study