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Genetics of depressive symptoms in adolescence
BACKGROUND: Despite many attempts to understand the genetic architecture of depression, little progress has been made. The majority of these studies, however, have been carried out in adults and do not account for the potential influence of development. METHODS: The Avon Longitudinal Study of Parent...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580280/ https://www.ncbi.nlm.nih.gov/pubmed/28859627 http://dx.doi.org/10.1186/s12888-017-1484-y |
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author | Sallis, Hannah Evans, Jonathan Wootton, Robyn Krapohl, Eva Oldehinkel, Albertine J Davey Smith, George Paternoster, Lavinia |
author_facet | Sallis, Hannah Evans, Jonathan Wootton, Robyn Krapohl, Eva Oldehinkel, Albertine J Davey Smith, George Paternoster, Lavinia |
author_sort | Sallis, Hannah |
collection | PubMed |
description | BACKGROUND: Despite many attempts to understand the genetic architecture of depression, little progress has been made. The majority of these studies, however, have been carried out in adults and do not account for the potential influence of development. METHODS: The Avon Longitudinal Study of Parents and Children (ALSPAC) is a longitudinal pregnancy cohort which recruited participants between April 1991 and December 1992. Analyses were replicated in two independent European cohorts. Genome-wide complex trait analysis (GCTA) software was used to investigate SNP-heritability (h(2) (SNP)) of depression across adolescence, the role of puberty was investigated by stratifying these estimates according to pubertal onset. Genome-wide association studies were performed to identify genetic variants associated with depression at different stages of development. RESULTS: Heritability was estimated between the ages of 11 and 18 with sample sizes ranging from 3289 to 5480. Heritability was low with an apparent peak was found at age 13 (h(2) = 0.17, p = 0.006). Confidence intervals around these estimates suggest an upper-bound to h(2) (SNP) of around 30%. A variant located on chromosome 7 was found to be associated with depressive symptoms at age 13 in ALSPAC (rs138191010: β = 0.142, p = 2.51 × 10(−8)), although this was not replicated. CONCLUSIONS: Although power is a potential limitation, the observed patterns provide interesting hypotheses surrounding the heritability of depression at different developmental stages. We found substantially lower estimates for depressive symptoms at age 11 (0.07) compared to those previously estimated in adults (0.21). We also found a peak in heritability at age 13. These findings suggest environmental factors are likely to be more important in the aetiology of depressive symptoms in early adolescence than in adulthood. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12888-017-1484-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5580280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55802802017-09-07 Genetics of depressive symptoms in adolescence Sallis, Hannah Evans, Jonathan Wootton, Robyn Krapohl, Eva Oldehinkel, Albertine J Davey Smith, George Paternoster, Lavinia BMC Psychiatry Research Article BACKGROUND: Despite many attempts to understand the genetic architecture of depression, little progress has been made. The majority of these studies, however, have been carried out in adults and do not account for the potential influence of development. METHODS: The Avon Longitudinal Study of Parents and Children (ALSPAC) is a longitudinal pregnancy cohort which recruited participants between April 1991 and December 1992. Analyses were replicated in two independent European cohorts. Genome-wide complex trait analysis (GCTA) software was used to investigate SNP-heritability (h(2) (SNP)) of depression across adolescence, the role of puberty was investigated by stratifying these estimates according to pubertal onset. Genome-wide association studies were performed to identify genetic variants associated with depression at different stages of development. RESULTS: Heritability was estimated between the ages of 11 and 18 with sample sizes ranging from 3289 to 5480. Heritability was low with an apparent peak was found at age 13 (h(2) = 0.17, p = 0.006). Confidence intervals around these estimates suggest an upper-bound to h(2) (SNP) of around 30%. A variant located on chromosome 7 was found to be associated with depressive symptoms at age 13 in ALSPAC (rs138191010: β = 0.142, p = 2.51 × 10(−8)), although this was not replicated. CONCLUSIONS: Although power is a potential limitation, the observed patterns provide interesting hypotheses surrounding the heritability of depression at different developmental stages. We found substantially lower estimates for depressive symptoms at age 11 (0.07) compared to those previously estimated in adults (0.21). We also found a peak in heritability at age 13. These findings suggest environmental factors are likely to be more important in the aetiology of depressive symptoms in early adolescence than in adulthood. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12888-017-1484-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-31 /pmc/articles/PMC5580280/ /pubmed/28859627 http://dx.doi.org/10.1186/s12888-017-1484-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Sallis, Hannah Evans, Jonathan Wootton, Robyn Krapohl, Eva Oldehinkel, Albertine J Davey Smith, George Paternoster, Lavinia Genetics of depressive symptoms in adolescence |
title | Genetics of depressive symptoms in adolescence |
title_full | Genetics of depressive symptoms in adolescence |
title_fullStr | Genetics of depressive symptoms in adolescence |
title_full_unstemmed | Genetics of depressive symptoms in adolescence |
title_short | Genetics of depressive symptoms in adolescence |
title_sort | genetics of depressive symptoms in adolescence |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580280/ https://www.ncbi.nlm.nih.gov/pubmed/28859627 http://dx.doi.org/10.1186/s12888-017-1484-y |
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