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An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans

OBJECTIVE: To examine the association between the 5-HTTLPR polymorphism of the serotonin transporter (SLC6A4) gene, combat exposure, and posttraumatic stress disorder (PTSD) diagnosis and among two samples of combat-exposed veterans. METHOD: The first sample included 550 non-Hispanic Black (NHB) com...

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Autores principales: Liu, Yutao, Garrett, Melanie E., Dennis, Michelle F., Green, Kimberly T., Ashley-Koch, Allison E., Hauser, Michael A., Beckham, Jean C., Kimbrel, Nathan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368771/
https://www.ncbi.nlm.nih.gov/pubmed/25793742
http://dx.doi.org/10.1371/journal.pone.0119998
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author Liu, Yutao
Garrett, Melanie E.
Dennis, Michelle F.
Green, Kimberly T.
Ashley-Koch, Allison E.
Hauser, Michael A.
Beckham, Jean C.
Kimbrel, Nathan A.
author_facet Liu, Yutao
Garrett, Melanie E.
Dennis, Michelle F.
Green, Kimberly T.
Ashley-Koch, Allison E.
Hauser, Michael A.
Beckham, Jean C.
Kimbrel, Nathan A.
author_sort Liu, Yutao
collection PubMed
description OBJECTIVE: To examine the association between the 5-HTTLPR polymorphism of the serotonin transporter (SLC6A4) gene, combat exposure, and posttraumatic stress disorder (PTSD) diagnosis and among two samples of combat-exposed veterans. METHOD: The first sample included 550 non-Hispanic Black (NHB) combat-exposed veterans. The second sample included 555 non-Hispanic White (NHW) combat-exposed veterans. Participants were genotyped for the 5-HTTLPR/rs25531 variants of the SLC6A4 gene. A structured clinical interview was used to diagnose PTSD. Combat and civilian trauma exposure were assessed with validated self-report instruments. Logistic regression was used to test for main effects of 5-HTTLPR on PTSD diagnosis as well as gene x environment (GxE) interactions after adjusting for sex, ancestry proportion scores, civilian trauma exposure, and combat exposure. RESULTS: Within the NHB sample, a significant additive effect was observed for 5-HTTLPR (OR = 1.502, p = .0025), such that the odds of having a current diagnosis of PTSD increased by 1.502 for each additional S’ allele. No evidence for an association between 5-HTTLPR and PTSD was observed in the NHW sample. In addition, no evidence for combat x 5-HTTLPR effects were observed in either sample. CONCLUSION: The present study suggests that there may be an association between 5-HTTLPR genotype and PTSD diagnosis among NHB veterans; however, no evidence for the hypothesized 5-HTTLPR x combat interaction was found.
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spelling pubmed-43687712015-03-27 An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans Liu, Yutao Garrett, Melanie E. Dennis, Michelle F. Green, Kimberly T. Ashley-Koch, Allison E. Hauser, Michael A. Beckham, Jean C. Kimbrel, Nathan A. PLoS One Research Article OBJECTIVE: To examine the association between the 5-HTTLPR polymorphism of the serotonin transporter (SLC6A4) gene, combat exposure, and posttraumatic stress disorder (PTSD) diagnosis and among two samples of combat-exposed veterans. METHOD: The first sample included 550 non-Hispanic Black (NHB) combat-exposed veterans. The second sample included 555 non-Hispanic White (NHW) combat-exposed veterans. Participants were genotyped for the 5-HTTLPR/rs25531 variants of the SLC6A4 gene. A structured clinical interview was used to diagnose PTSD. Combat and civilian trauma exposure were assessed with validated self-report instruments. Logistic regression was used to test for main effects of 5-HTTLPR on PTSD diagnosis as well as gene x environment (GxE) interactions after adjusting for sex, ancestry proportion scores, civilian trauma exposure, and combat exposure. RESULTS: Within the NHB sample, a significant additive effect was observed for 5-HTTLPR (OR = 1.502, p = .0025), such that the odds of having a current diagnosis of PTSD increased by 1.502 for each additional S’ allele. No evidence for an association between 5-HTTLPR and PTSD was observed in the NHW sample. In addition, no evidence for combat x 5-HTTLPR effects were observed in either sample. CONCLUSION: The present study suggests that there may be an association between 5-HTTLPR genotype and PTSD diagnosis among NHB veterans; however, no evidence for the hypothesized 5-HTTLPR x combat interaction was found. Public Library of Science 2015-03-20 /pmc/articles/PMC4368771/ /pubmed/25793742 http://dx.doi.org/10.1371/journal.pone.0119998 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Liu, Yutao
Garrett, Melanie E.
Dennis, Michelle F.
Green, Kimberly T.
Ashley-Koch, Allison E.
Hauser, Michael A.
Beckham, Jean C.
Kimbrel, Nathan A.
An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans
title An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans
title_full An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans
title_fullStr An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans
title_full_unstemmed An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans
title_short An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans
title_sort examination of the association between 5-httlpr, combat exposure, and ptsd diagnosis among u.s. veterans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368771/
https://www.ncbi.nlm.nih.gov/pubmed/25793742
http://dx.doi.org/10.1371/journal.pone.0119998
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