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Associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural Australians
PURPOSE: Depression remains difficult to treat in all cases, and further investigation of the role of genetic and environmental factors may be valuable. This study was designed to investigate the association between the short (s) versus non-short (non-s) 5HTTLPR variants, presence of childhood stres...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091248/ https://www.ncbi.nlm.nih.gov/pubmed/30127611 http://dx.doi.org/10.2147/NDT.S168291 |
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author | Sharpley, Christopher F Bitsika, Vicki McMillan, Mary E Jesulola, Emmanuel Agnew, Linda L |
author_facet | Sharpley, Christopher F Bitsika, Vicki McMillan, Mary E Jesulola, Emmanuel Agnew, Linda L |
author_sort | Sharpley, Christopher F |
collection | PubMed |
description | PURPOSE: Depression remains difficult to treat in all cases, and further investigation of the role of genetic and environmental factors may be valuable. This study was designed to investigate the association between the short (s) versus non-short (non-s) 5HTTLPR variants, presence of childhood stressors and recent life stressors, and depression, and to do so at two levels that would expose the associations between total depression scores and also individual depression items. MATERIALS AND METHODS: Two hundred and forty-nine volunteers from one of the Australian Electoral Office electorates covering a large rural land area completed a series of questionnaires about childhood and recent life stress and depression, and provided a buccal cell sample for genotyping the 5-HTTLPR polymorphism into s versus non-s carriers. RESULTS: Although there were no significant differences in the depression scores of the s-carriers versus the non-s carriers, each subtype of the 5-HTTLPR polymorphism showed different patterns of association between childhood stress and depression symptoms, and between recent life stress and depression symptoms. CONCLUSION: Individualization of therapy for depression may be achieved through consideration of the specific associations that patients exhibit between life stress, 5-HTTLPR polymorphism, and depression symptomatology. |
format | Online Article Text |
id | pubmed-6091248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60912482018-08-20 Associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural Australians Sharpley, Christopher F Bitsika, Vicki McMillan, Mary E Jesulola, Emmanuel Agnew, Linda L Neuropsychiatr Dis Treat Original Research PURPOSE: Depression remains difficult to treat in all cases, and further investigation of the role of genetic and environmental factors may be valuable. This study was designed to investigate the association between the short (s) versus non-short (non-s) 5HTTLPR variants, presence of childhood stressors and recent life stressors, and depression, and to do so at two levels that would expose the associations between total depression scores and also individual depression items. MATERIALS AND METHODS: Two hundred and forty-nine volunteers from one of the Australian Electoral Office electorates covering a large rural land area completed a series of questionnaires about childhood and recent life stress and depression, and provided a buccal cell sample for genotyping the 5-HTTLPR polymorphism into s versus non-s carriers. RESULTS: Although there were no significant differences in the depression scores of the s-carriers versus the non-s carriers, each subtype of the 5-HTTLPR polymorphism showed different patterns of association between childhood stress and depression symptoms, and between recent life stress and depression symptoms. CONCLUSION: Individualization of therapy for depression may be achieved through consideration of the specific associations that patients exhibit between life stress, 5-HTTLPR polymorphism, and depression symptomatology. Dove Medical Press 2018-08-10 /pmc/articles/PMC6091248/ /pubmed/30127611 http://dx.doi.org/10.2147/NDT.S168291 Text en © 2018 Sharpley et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Sharpley, Christopher F Bitsika, Vicki McMillan, Mary E Jesulola, Emmanuel Agnew, Linda L Associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural Australians |
title | Associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural Australians |
title_full | Associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural Australians |
title_fullStr | Associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural Australians |
title_full_unstemmed | Associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural Australians |
title_short | Associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural Australians |
title_sort | associations between stress and depression symptom profiles vary according to serotonin transporter polymorphism in rural australians |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091248/ https://www.ncbi.nlm.nih.gov/pubmed/30127611 http://dx.doi.org/10.2147/NDT.S168291 |
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