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Interaction between SLC6A4 promoter variants and childhood trauma on the age at onset of bipolar disorders
Age at onset (AAO) of bipolar disorders (BD) could be influenced both by a repeat length polymorphism (5HTTLPR) in the promoter region of the serotonin transporter gene (SLC6A4) and exposure to childhood trauma. We assessed 308 euthymic patients with BD for the AAO of their first mood episode and ch...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635347/ https://www.ncbi.nlm.nih.gov/pubmed/26542422 http://dx.doi.org/10.1038/srep16301 |
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author | Etain, B. Lajnef, M. Henrion, A. Dargél, A.A. Stertz, L. Kapczinski, F. Mathieu, F. Henry, C. Gard, S. Kahn, J. P. Leboyer, M. Jamain, S. Bellivier, F. |
author_facet | Etain, B. Lajnef, M. Henrion, A. Dargél, A.A. Stertz, L. Kapczinski, F. Mathieu, F. Henry, C. Gard, S. Kahn, J. P. Leboyer, M. Jamain, S. Bellivier, F. |
author_sort | Etain, B. |
collection | PubMed |
description | Age at onset (AAO) of bipolar disorders (BD) could be influenced both by a repeat length polymorphism (5HTTLPR) in the promoter region of the serotonin transporter gene (SLC6A4) and exposure to childhood trauma. We assessed 308 euthymic patients with BD for the AAO of their first mood episode and childhood trauma. Patients were genotyped for the 5HTTLPR (long/short variant) and the rs25531. Genotypes were classified on functional significance (LL, LS, SS). A sample of 126 Brazilian euthymic patients with BD was used for replication. In the French sample, the correlation between AAO and trauma score was observed only among ‘SS’ homozygotes (p = 0.002) but not among ‘L’ allele carriers. A history of at least one trauma decreased the AAO only in ‘SS’ homozygotes (p = 0.001). These results remained significant after correction using FDR. Regression models suggested an interaction between emotional neglect and ‘SS’ genotype on the AAO (p = 0.009) and no further interaction with other trauma subtypes. Partial replication was obtained in the Brazilian sample, showing an interaction between emotional abuse and ‘LS’ genotype on the AAO (p = 0.02). In conclusion, an effect of childhood trauma on AAO of BD was observed only in patients who carry a specific stress responsiveness-related SLC6A4 promoter genotype. |
format | Online Article Text |
id | pubmed-4635347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46353472015-11-25 Interaction between SLC6A4 promoter variants and childhood trauma on the age at onset of bipolar disorders Etain, B. Lajnef, M. Henrion, A. Dargél, A.A. Stertz, L. Kapczinski, F. Mathieu, F. Henry, C. Gard, S. Kahn, J. P. Leboyer, M. Jamain, S. Bellivier, F. Sci Rep Article Age at onset (AAO) of bipolar disorders (BD) could be influenced both by a repeat length polymorphism (5HTTLPR) in the promoter region of the serotonin transporter gene (SLC6A4) and exposure to childhood trauma. We assessed 308 euthymic patients with BD for the AAO of their first mood episode and childhood trauma. Patients were genotyped for the 5HTTLPR (long/short variant) and the rs25531. Genotypes were classified on functional significance (LL, LS, SS). A sample of 126 Brazilian euthymic patients with BD was used for replication. In the French sample, the correlation between AAO and trauma score was observed only among ‘SS’ homozygotes (p = 0.002) but not among ‘L’ allele carriers. A history of at least one trauma decreased the AAO only in ‘SS’ homozygotes (p = 0.001). These results remained significant after correction using FDR. Regression models suggested an interaction between emotional neglect and ‘SS’ genotype on the AAO (p = 0.009) and no further interaction with other trauma subtypes. Partial replication was obtained in the Brazilian sample, showing an interaction between emotional abuse and ‘LS’ genotype on the AAO (p = 0.02). In conclusion, an effect of childhood trauma on AAO of BD was observed only in patients who carry a specific stress responsiveness-related SLC6A4 promoter genotype. Nature Publishing Group 2015-11-06 /pmc/articles/PMC4635347/ /pubmed/26542422 http://dx.doi.org/10.1038/srep16301 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Etain, B. Lajnef, M. Henrion, A. Dargél, A.A. Stertz, L. Kapczinski, F. Mathieu, F. Henry, C. Gard, S. Kahn, J. P. Leboyer, M. Jamain, S. Bellivier, F. Interaction between SLC6A4 promoter variants and childhood trauma on the age at onset of bipolar disorders |
title | Interaction between SLC6A4 promoter variants and childhood trauma on the age at onset of bipolar disorders |
title_full | Interaction between SLC6A4 promoter variants and childhood trauma on the age at onset of bipolar disorders |
title_fullStr | Interaction between SLC6A4 promoter variants and childhood trauma on the age at onset of bipolar disorders |
title_full_unstemmed | Interaction between SLC6A4 promoter variants and childhood trauma on the age at onset of bipolar disorders |
title_short | Interaction between SLC6A4 promoter variants and childhood trauma on the age at onset of bipolar disorders |
title_sort | interaction between slc6a4 promoter variants and childhood trauma on the age at onset of bipolar disorders |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635347/ https://www.ncbi.nlm.nih.gov/pubmed/26542422 http://dx.doi.org/10.1038/srep16301 |
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