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Depressive symptoms during adolescence: comparison between epidemiological and high risk sampling

PURPOSE: Both epidemiological (unselected) and high risk (screening on known risk criteria) samplings have been used to investigate the course of affective disorders. Selecting individuals on multiple risk criteria may create a sample not comparable to individuals with similar risk criteria within t...

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Autores principales: St Clair, Michelle C., Goodyer, Ian M., Dunn, Valerie, Herbert, Joe, Jones, Peter B., Croudace, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399078/
https://www.ncbi.nlm.nih.gov/pubmed/22037558
http://dx.doi.org/10.1007/s00127-011-0441-1
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author St Clair, Michelle C.
Goodyer, Ian M.
Dunn, Valerie
Herbert, Joe
Jones, Peter B.
Croudace, Tim
author_facet St Clair, Michelle C.
Goodyer, Ian M.
Dunn, Valerie
Herbert, Joe
Jones, Peter B.
Croudace, Tim
author_sort St Clair, Michelle C.
collection PubMed
description PURPOSE: Both epidemiological (unselected) and high risk (screening on known risk criteria) samplings have been used to investigate the course of affective disorders. Selecting individuals on multiple risk criteria may create a sample not comparable to individuals with similar risk criteria within the general population. This study compared depressive symptoms across the two sampling methods to test this possibility. METHODS: The high risk Cambridge Hormones and Moods Project (CHAMP) screened and recruited adolescents aged 12 to 16. A total of 905 (710 high risk) individuals participated and were reassessed at three follow-ups. The ROOTS epidemiological sample consisted of 1,208 14-year-olds reassessed at 15.5 and 17 years. The risk profile for CHAMP was recreated in the ROOTS study. Both samples completed the Moods and Feelings Questionnaire, a self-report measure of current depressive symptoms. RESULTS: Comparing individuals with the same high risk profiles across the CHAMP and ROOTS studies revealed no significant differences in mean depression scores. Combining the samples revealed that for females, mean depression scores were maintained from 12 to 15 years then declined by 17 years. For males, scores declined from 12 throughout adolescence. High risk status led to consistently higher levels of depressive symptoms in female adolescents but result in little change within male adolescents. CONCLUSIONS: The high risk design recruited adolescents with a depression symptoms profile comparable to the general population for both sexes. High risk status may alter the trajectory of depressive symptoms in female adolescents only. Males may be less sensitive to recent adversity.
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spelling pubmed-33990782012-07-25 Depressive symptoms during adolescence: comparison between epidemiological and high risk sampling St Clair, Michelle C. Goodyer, Ian M. Dunn, Valerie Herbert, Joe Jones, Peter B. Croudace, Tim Soc Psychiatry Psychiatr Epidemiol Original Paper PURPOSE: Both epidemiological (unselected) and high risk (screening on known risk criteria) samplings have been used to investigate the course of affective disorders. Selecting individuals on multiple risk criteria may create a sample not comparable to individuals with similar risk criteria within the general population. This study compared depressive symptoms across the two sampling methods to test this possibility. METHODS: The high risk Cambridge Hormones and Moods Project (CHAMP) screened and recruited adolescents aged 12 to 16. A total of 905 (710 high risk) individuals participated and were reassessed at three follow-ups. The ROOTS epidemiological sample consisted of 1,208 14-year-olds reassessed at 15.5 and 17 years. The risk profile for CHAMP was recreated in the ROOTS study. Both samples completed the Moods and Feelings Questionnaire, a self-report measure of current depressive symptoms. RESULTS: Comparing individuals with the same high risk profiles across the CHAMP and ROOTS studies revealed no significant differences in mean depression scores. Combining the samples revealed that for females, mean depression scores were maintained from 12 to 15 years then declined by 17 years. For males, scores declined from 12 throughout adolescence. High risk status led to consistently higher levels of depressive symptoms in female adolescents but result in little change within male adolescents. CONCLUSIONS: The high risk design recruited adolescents with a depression symptoms profile comparable to the general population for both sexes. High risk status may alter the trajectory of depressive symptoms in female adolescents only. Males may be less sensitive to recent adversity. Springer-Verlag 2011-10-30 2012 /pmc/articles/PMC3399078/ /pubmed/22037558 http://dx.doi.org/10.1007/s00127-011-0441-1 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
St Clair, Michelle C.
Goodyer, Ian M.
Dunn, Valerie
Herbert, Joe
Jones, Peter B.
Croudace, Tim
Depressive symptoms during adolescence: comparison between epidemiological and high risk sampling
title Depressive symptoms during adolescence: comparison between epidemiological and high risk sampling
title_full Depressive symptoms during adolescence: comparison between epidemiological and high risk sampling
title_fullStr Depressive symptoms during adolescence: comparison between epidemiological and high risk sampling
title_full_unstemmed Depressive symptoms during adolescence: comparison between epidemiological and high risk sampling
title_short Depressive symptoms during adolescence: comparison between epidemiological and high risk sampling
title_sort depressive symptoms during adolescence: comparison between epidemiological and high risk sampling
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399078/
https://www.ncbi.nlm.nih.gov/pubmed/22037558
http://dx.doi.org/10.1007/s00127-011-0441-1
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