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Genetic Risk for Psychiatric Disorders and Telomere Length
Background: Previous studies have revealed associations between psychiatric disorder diagnosis and shorter telomere length. Here, we attempt to discern whether genetic risk for psychiatric disorders, or use of pharmacological treatments (i.e., antidepressants), predict shorter telomere length and ri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232668/ https://www.ncbi.nlm.nih.gov/pubmed/30459805 http://dx.doi.org/10.3389/fgene.2018.00468 |
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author | Palmos, Alish B. Breen, Gerome Goodwin, Laura Frissa, Souci Hatch, Stephani L. Hotopf, Matthew Thuret, Sandrine Lewis, Cathryn M. Powell, Timothy R. |
author_facet | Palmos, Alish B. Breen, Gerome Goodwin, Laura Frissa, Souci Hatch, Stephani L. Hotopf, Matthew Thuret, Sandrine Lewis, Cathryn M. Powell, Timothy R. |
author_sort | Palmos, Alish B. |
collection | PubMed |
description | Background: Previous studies have revealed associations between psychiatric disorder diagnosis and shorter telomere length. Here, we attempt to discern whether genetic risk for psychiatric disorders, or use of pharmacological treatments (i.e., antidepressants), predict shorter telomere length and risk for aging-related disease in a United Kingdom population sample. Methods: DNA samples from blood were available from 351 participants who were recruited as part of the South East London Community Health (SELCoH) Study, and for which whole-genome genotype data was available. Leukocyte telomere length was characterized using quantitative polymerase chain reactions. Individualized polygenic risk scores for major depressive disorder (MDD), bipolar disorder (BD), and schizophrenia (SCZ) were calculated using Psychiatric Genomics Consortium summary statistics. We subsequently performed linear models, to discern the impact polygenic risk for psychiatric disorders (an etiological risk factor) and antidepressant use (common pharmacological treatment) have on telomere length, whilst accounting for other lifestyle/health factors (e.g., BMI, smoking). Results: There were no significant associations between polygenic risk for any of the psychiatric disorders tested and telomere length (p > 0.05). Antidepressant use was significantly associated with shorter telomere length and this was independent from a depression diagnosis or current depression severity (p ≤ 0.01). Antidepressant use was also associated with a significantly higher risk of aging-related disease, which was independent from depression diagnosis (p ≤ 0.05). Conclusion: Genetic risk for psychiatric disorders is not associated with shorter telomere length. Further studies are now needed to prospectively characterize if antidepressant use increases risk for aging-related disease and telomere shortening, or whether people who age faster and have aging-related diseases are just more likely to be prescribed antidepressants. |
format | Online Article Text |
id | pubmed-6232668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62326682018-11-20 Genetic Risk for Psychiatric Disorders and Telomere Length Palmos, Alish B. Breen, Gerome Goodwin, Laura Frissa, Souci Hatch, Stephani L. Hotopf, Matthew Thuret, Sandrine Lewis, Cathryn M. Powell, Timothy R. Front Genet Genetics Background: Previous studies have revealed associations between psychiatric disorder diagnosis and shorter telomere length. Here, we attempt to discern whether genetic risk for psychiatric disorders, or use of pharmacological treatments (i.e., antidepressants), predict shorter telomere length and risk for aging-related disease in a United Kingdom population sample. Methods: DNA samples from blood were available from 351 participants who were recruited as part of the South East London Community Health (SELCoH) Study, and for which whole-genome genotype data was available. Leukocyte telomere length was characterized using quantitative polymerase chain reactions. Individualized polygenic risk scores for major depressive disorder (MDD), bipolar disorder (BD), and schizophrenia (SCZ) were calculated using Psychiatric Genomics Consortium summary statistics. We subsequently performed linear models, to discern the impact polygenic risk for psychiatric disorders (an etiological risk factor) and antidepressant use (common pharmacological treatment) have on telomere length, whilst accounting for other lifestyle/health factors (e.g., BMI, smoking). Results: There were no significant associations between polygenic risk for any of the psychiatric disorders tested and telomere length (p > 0.05). Antidepressant use was significantly associated with shorter telomere length and this was independent from a depression diagnosis or current depression severity (p ≤ 0.01). Antidepressant use was also associated with a significantly higher risk of aging-related disease, which was independent from depression diagnosis (p ≤ 0.05). Conclusion: Genetic risk for psychiatric disorders is not associated with shorter telomere length. Further studies are now needed to prospectively characterize if antidepressant use increases risk for aging-related disease and telomere shortening, or whether people who age faster and have aging-related diseases are just more likely to be prescribed antidepressants. Frontiers Media S.A. 2018-10-16 /pmc/articles/PMC6232668/ /pubmed/30459805 http://dx.doi.org/10.3389/fgene.2018.00468 Text en Copyright © 2018 Palmos, Breen, Goodwin, Frissa, Hatch, Hotopf, Thuret, Lewis and Powell. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Palmos, Alish B. Breen, Gerome Goodwin, Laura Frissa, Souci Hatch, Stephani L. Hotopf, Matthew Thuret, Sandrine Lewis, Cathryn M. Powell, Timothy R. Genetic Risk for Psychiatric Disorders and Telomere Length |
title | Genetic Risk for Psychiatric Disorders and Telomere Length |
title_full | Genetic Risk for Psychiatric Disorders and Telomere Length |
title_fullStr | Genetic Risk for Psychiatric Disorders and Telomere Length |
title_full_unstemmed | Genetic Risk for Psychiatric Disorders and Telomere Length |
title_short | Genetic Risk for Psychiatric Disorders and Telomere Length |
title_sort | genetic risk for psychiatric disorders and telomere length |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232668/ https://www.ncbi.nlm.nih.gov/pubmed/30459805 http://dx.doi.org/10.3389/fgene.2018.00468 |
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