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Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach

BACKGROUND: Data from clinical studies and results from animal models suggest an involvement of the neurotrophin system in the pathology of depression and antidepressant treatment response. Genetic variations within the genes coding for the brain-derived neurotrophic factor (BDNF) and its key recept...

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Autores principales: Hennings, Johannes M., Kohli, Martin A., Czamara, Darina, Giese, Maria, Eckert, Anne, Wolf, Christiane, Heck, Angela, Domschke, Katharina, Arolt, Volker, Baune, Bernhard T., Horstmann, Sonja, Brückl, Tanja, Klengel, Torsten, Menke, Andreas, Müller-Myhsok, Bertram, Ising, Marcus, Uhr, Manfred, Lucae, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672143/
https://www.ncbi.nlm.nih.gov/pubmed/23750220
http://dx.doi.org/10.1371/journal.pone.0064947
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author Hennings, Johannes M.
Kohli, Martin A.
Czamara, Darina
Giese, Maria
Eckert, Anne
Wolf, Christiane
Heck, Angela
Domschke, Katharina
Arolt, Volker
Baune, Bernhard T.
Horstmann, Sonja
Brückl, Tanja
Klengel, Torsten
Menke, Andreas
Müller-Myhsok, Bertram
Ising, Marcus
Uhr, Manfred
Lucae, Susanne
author_facet Hennings, Johannes M.
Kohli, Martin A.
Czamara, Darina
Giese, Maria
Eckert, Anne
Wolf, Christiane
Heck, Angela
Domschke, Katharina
Arolt, Volker
Baune, Bernhard T.
Horstmann, Sonja
Brückl, Tanja
Klengel, Torsten
Menke, Andreas
Müller-Myhsok, Bertram
Ising, Marcus
Uhr, Manfred
Lucae, Susanne
author_sort Hennings, Johannes M.
collection PubMed
description BACKGROUND: Data from clinical studies and results from animal models suggest an involvement of the neurotrophin system in the pathology of depression and antidepressant treatment response. Genetic variations within the genes coding for the brain-derived neurotrophic factor (BDNF) and its key receptor Trkb (NTRK2) may therefore influence the response to antidepressant treatment. METHODS: We performed a single and multi-marker association study with antidepressant treatment outcome in 398 depressed Caucasian inpatients participating in the Munich Antidepressant Response Signature (MARS) project. Two Caucasian replication samples (N = 249 and N = 247) were investigated, resulting in a total number of 894 patients. 18 tagging SNPs in the BDNF gene region and 64 tagging SNPs in the NTRK2 gene region were genotyped in the discovery sample; 16 nominally associated SNPs were tested in two replication samples. RESULTS: In the discovery analysis, 7 BDNF SNPs and 9 NTRK2 SNPs were nominally associated with treatment response. Three NTRK2 SNPs (rs10868223, rs1659412 and rs11140778) also showed associations in at least one replication sample and in the combined sample with the same direction of effects (P(corr) = .018, P(corr) = .015 and P(corr) = .004, respectively). We observed an across-gene BDNF-NTRK2 SNP interaction for rs4923468 and rs1387926. No robust interaction of associated SNPs was found in an analysis of BDNF serum protein levels as a predictor for treatment outcome in a subset of 93 patients. CONCLUSIONS/LIMITATIONS: Although not all associations in the discovery analysis could be unambiguously replicated, the findings of the present study identified single nucleotide variations in the BDNF and NTRK2 genes that might be involved in antidepressant treatment outcome and that have not been previously reported in this context. These new variants need further validation in future association studies.
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spelling pubmed-36721432013-06-07 Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach Hennings, Johannes M. Kohli, Martin A. Czamara, Darina Giese, Maria Eckert, Anne Wolf, Christiane Heck, Angela Domschke, Katharina Arolt, Volker Baune, Bernhard T. Horstmann, Sonja Brückl, Tanja Klengel, Torsten Menke, Andreas Müller-Myhsok, Bertram Ising, Marcus Uhr, Manfred Lucae, Susanne PLoS One Research Article BACKGROUND: Data from clinical studies and results from animal models suggest an involvement of the neurotrophin system in the pathology of depression and antidepressant treatment response. Genetic variations within the genes coding for the brain-derived neurotrophic factor (BDNF) and its key receptor Trkb (NTRK2) may therefore influence the response to antidepressant treatment. METHODS: We performed a single and multi-marker association study with antidepressant treatment outcome in 398 depressed Caucasian inpatients participating in the Munich Antidepressant Response Signature (MARS) project. Two Caucasian replication samples (N = 249 and N = 247) were investigated, resulting in a total number of 894 patients. 18 tagging SNPs in the BDNF gene region and 64 tagging SNPs in the NTRK2 gene region were genotyped in the discovery sample; 16 nominally associated SNPs were tested in two replication samples. RESULTS: In the discovery analysis, 7 BDNF SNPs and 9 NTRK2 SNPs were nominally associated with treatment response. Three NTRK2 SNPs (rs10868223, rs1659412 and rs11140778) also showed associations in at least one replication sample and in the combined sample with the same direction of effects (P(corr) = .018, P(corr) = .015 and P(corr) = .004, respectively). We observed an across-gene BDNF-NTRK2 SNP interaction for rs4923468 and rs1387926. No robust interaction of associated SNPs was found in an analysis of BDNF serum protein levels as a predictor for treatment outcome in a subset of 93 patients. CONCLUSIONS/LIMITATIONS: Although not all associations in the discovery analysis could be unambiguously replicated, the findings of the present study identified single nucleotide variations in the BDNF and NTRK2 genes that might be involved in antidepressant treatment outcome and that have not been previously reported in this context. These new variants need further validation in future association studies. Public Library of Science 2013-06-04 /pmc/articles/PMC3672143/ /pubmed/23750220 http://dx.doi.org/10.1371/journal.pone.0064947 Text en © 2013 Hennings et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hennings, Johannes M.
Kohli, Martin A.
Czamara, Darina
Giese, Maria
Eckert, Anne
Wolf, Christiane
Heck, Angela
Domschke, Katharina
Arolt, Volker
Baune, Bernhard T.
Horstmann, Sonja
Brückl, Tanja
Klengel, Torsten
Menke, Andreas
Müller-Myhsok, Bertram
Ising, Marcus
Uhr, Manfred
Lucae, Susanne
Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach
title Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach
title_full Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach
title_fullStr Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach
title_full_unstemmed Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach
title_short Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach
title_sort possible associations of ntrk2 polymorphisms with antidepressant treatment outcome: findings from an extended tag snp approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672143/
https://www.ncbi.nlm.nih.gov/pubmed/23750220
http://dx.doi.org/10.1371/journal.pone.0064947
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