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Cohort profile: the Australian genetics of depression study
PURPOSE: Depression is the most common psychiatric disorder and the largest contributor to global disability. The Australian Genetics of Depression study was established to recruit a large cohort of individuals who have been diagnosed with depression at some point in their lifetime. The purpose of e...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259831/ https://www.ncbi.nlm.nih.gov/pubmed/32461290 http://dx.doi.org/10.1136/bmjopen-2019-032580 |
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author | Byrne, Enda M Kirk, Katherine M Medland, Sarah E McGrath, John J Colodro-Conde, Lucia Parker, Richard Cross, Simone Sullivan, Lenore Statham, Dixie J Levinson, Douglas F Licinio, Julio Wray, Naomi R Hickie, Ian B Martin, Nicholas G |
author_facet | Byrne, Enda M Kirk, Katherine M Medland, Sarah E McGrath, John J Colodro-Conde, Lucia Parker, Richard Cross, Simone Sullivan, Lenore Statham, Dixie J Levinson, Douglas F Licinio, Julio Wray, Naomi R Hickie, Ian B Martin, Nicholas G |
author_sort | Byrne, Enda M |
collection | PubMed |
description | PURPOSE: Depression is the most common psychiatric disorder and the largest contributor to global disability. The Australian Genetics of Depression study was established to recruit a large cohort of individuals who have been diagnosed with depression at some point in their lifetime. The purpose of establishing this cohort is to investigate genetic and environmental risk factors for depression and response to commonly prescribed antidepressants. PARTICIPANTS: A total of 20 689 participants were recruited through the Australian Department of Human Services and a media campaign, 75% of whom were female. The average age of participants was 43 years±15 years. Participants completed an online questionnaire that consisted of a compulsory module that assessed self-reported psychiatric history, clinical depression using the Composite Interview Diagnostic Interview Short Form and experiences of using commonly prescribed antidepressants. Further voluntary modules assessed a wide range of traits of relevance to psychopathology. Participants who reported they were willing to provide a DNA sample (75%) were sent a saliva kit in the mail. FINDINGS TO DATE: 95% of participants reported being given a diagnosis of depression by a medical practitioner and 88% met the criteria for a lifetime depressive episode. 68% of the sample report having been diagnosed with another psychiatric disorder in addition to depression. In line with findings from clinical trials, only 33% of the sample report responding well to the first antidepressant they were prescribed. FUTURE PLANS: A number of analyses to investigate the genetic architecture of depression and common comorbidities will be conducted. The cohort will contribute to the global effort to identify genetic variants that increase risk to depression. Furthermore, a thorough investigation of genetic and psychosocial predictors of antidepressant response and side effects is planned. |
format | Online Article Text |
id | pubmed-7259831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-72598312020-06-09 Cohort profile: the Australian genetics of depression study Byrne, Enda M Kirk, Katherine M Medland, Sarah E McGrath, John J Colodro-Conde, Lucia Parker, Richard Cross, Simone Sullivan, Lenore Statham, Dixie J Levinson, Douglas F Licinio, Julio Wray, Naomi R Hickie, Ian B Martin, Nicholas G BMJ Open Mental Health PURPOSE: Depression is the most common psychiatric disorder and the largest contributor to global disability. The Australian Genetics of Depression study was established to recruit a large cohort of individuals who have been diagnosed with depression at some point in their lifetime. The purpose of establishing this cohort is to investigate genetic and environmental risk factors for depression and response to commonly prescribed antidepressants. PARTICIPANTS: A total of 20 689 participants were recruited through the Australian Department of Human Services and a media campaign, 75% of whom were female. The average age of participants was 43 years±15 years. Participants completed an online questionnaire that consisted of a compulsory module that assessed self-reported psychiatric history, clinical depression using the Composite Interview Diagnostic Interview Short Form and experiences of using commonly prescribed antidepressants. Further voluntary modules assessed a wide range of traits of relevance to psychopathology. Participants who reported they were willing to provide a DNA sample (75%) were sent a saliva kit in the mail. FINDINGS TO DATE: 95% of participants reported being given a diagnosis of depression by a medical practitioner and 88% met the criteria for a lifetime depressive episode. 68% of the sample report having been diagnosed with another psychiatric disorder in addition to depression. In line with findings from clinical trials, only 33% of the sample report responding well to the first antidepressant they were prescribed. FUTURE PLANS: A number of analyses to investigate the genetic architecture of depression and common comorbidities will be conducted. The cohort will contribute to the global effort to identify genetic variants that increase risk to depression. Furthermore, a thorough investigation of genetic and psychosocial predictors of antidepressant response and side effects is planned. BMJ Publishing Group 2020-05-26 /pmc/articles/PMC7259831/ /pubmed/32461290 http://dx.doi.org/10.1136/bmjopen-2019-032580 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Mental Health Byrne, Enda M Kirk, Katherine M Medland, Sarah E McGrath, John J Colodro-Conde, Lucia Parker, Richard Cross, Simone Sullivan, Lenore Statham, Dixie J Levinson, Douglas F Licinio, Julio Wray, Naomi R Hickie, Ian B Martin, Nicholas G Cohort profile: the Australian genetics of depression study |
title | Cohort profile: the Australian genetics of depression study |
title_full | Cohort profile: the Australian genetics of depression study |
title_fullStr | Cohort profile: the Australian genetics of depression study |
title_full_unstemmed | Cohort profile: the Australian genetics of depression study |
title_short | Cohort profile: the Australian genetics of depression study |
title_sort | cohort profile: the australian genetics of depression study |
topic | Mental Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259831/ https://www.ncbi.nlm.nih.gov/pubmed/32461290 http://dx.doi.org/10.1136/bmjopen-2019-032580 |
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