Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/65741
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Type: Journal article
Title: The Interleukin 1 Beta (IL1B) Gene Is Associated with Failure to Achieve Remission and Impaired Emotion Processing in Major Depression
Author: Baune, B.
Dannlowski, U.
Domschke, K.
Janssen, D.
Jordan, M.
Ohrmann, P.
Bauer, J.
Biros, E.
Arolt, V.
Kugel, H.
Baxter, A.
Suslow, T.
Citation: Biological Psychiatry, 2010; 67(6):543-549
Publisher: Elsevier Science Inc
Issue Date: 2010
ISSN: 0006-3223
1873-2402
Statement of
Responsibility: 
Bernhard T. Baune, Udo Dannlowski, Katharina Domschke, Debbie G.A. Janssen, Margaret A. Jordan, Patricia Ohrmann, Jochen Bauer, Erik Biros, Volker Arolt, Harald Kugel, Alan G. Baxter, and Thomas Suslow
Abstract: Background: Accumulating evidence suggests the involvement of inflammatory processes and cytokines in particular in the pathophysiology of major depression (MDD) and resistance to antidepressant treatment. Furthermore, amygdala and anterior cingulate cortex (ACC) responsiveness to emotional stimuli has been suggested as a predictor of treatment response. This study investigated the association between genetic variants of the interleukin 1 beta (IL1B) gene and amygdala and ACC responsiveness to emotional stimuli and response to antidepressant treatment. Methods: In this analysis, 256 Caucasian patients with MDD (145 women, 111 men) were genotyped for variants rs16944, rs1143643, and rs1143634 in the IL1B gene (2q14). Response to antidepressant treatment over 6 weeks was defined as remission (≤ 7 on the Hamilton Rating Scale for Depression–21-question) and response (>50% decrease on Hamilton Rating Scale for Depression–21-question). Brain activity under visual presentation of emotional faces was assessed in a subsample of 32 depressed patients by means of functional magnetic resonance imaging at 3 T. Results: Pharmacogenetic analyses show significant associations of the GG genotypes of single nucleotide polymorphisms (SNPs) rs16944 (odds ratio = 1.74; 95% confidence interval 1.2–4.3) and rs1143643 (odds ratio = 3.1; 95% confidence interval 1.3–7.8) (compared with the AA genotype) with nonremission after 6 weeks. The imaging analyses show that the number of G-alleles in both SNPs (rs16944 and rs1143643) was associated with reduced responsiveness of the amygdala and ACC to emotional stimulation. Conclusions: The present study suggests a negative effect of the IL1B gene on pharmacological response and amygdala and ACC function involving the same genotypes of two SNPs (rs16944, rs116343), which taken together increase the risk of nonremission over 6 weeks of antidepressant treatment in MDD.
Keywords: Amygdala and cingulate; antidepressant treatment response; depression; inflammation; interleukin 1 beta; pharmacogenetics
Rights: © 2010 Society of Biological Psychiatry
RMID: 0020111322
DOI: 10.1016/j.biopsych.2009.11.004
Appears in Collections:Psychiatry publications

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