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National cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age

BACKGROUND: Psychiatric illness, substance misuse, suicidality, criminality and premature death represent major public health challenges that afflict a sizeable proportion of young people. However, studies of multiple adverse outcomes in the same cohort at risk are rare. In a national Danish cohort...

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Autores principales: Mok, Pearl L.H., Antonsen, Sussie, Pedersen, Carsten Bøcker, Appleby, Louis, Shaw, Jenny, Webb, Roger T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575432/
https://www.ncbi.nlm.nih.gov/pubmed/26386672
http://dx.doi.org/10.1186/s12889-015-2249-5
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author Mok, Pearl L.H.
Antonsen, Sussie
Pedersen, Carsten Bøcker
Appleby, Louis
Shaw, Jenny
Webb, Roger T.
author_facet Mok, Pearl L.H.
Antonsen, Sussie
Pedersen, Carsten Bøcker
Appleby, Louis
Shaw, Jenny
Webb, Roger T.
author_sort Mok, Pearl L.H.
collection PubMed
description BACKGROUND: Psychiatric illness, substance misuse, suicidality, criminality and premature death represent major public health challenges that afflict a sizeable proportion of young people. However, studies of multiple adverse outcomes in the same cohort at risk are rare. In a national Danish cohort we estimated sex- and age-specific incidence rates and absolute risks of these outcomes between adolescence and early middle age. METHODS: Using interlinked registers, persons born in Denmark 1966–1996 were followed from their 15(th) until 40(th) birthday or December 2011 (N = 2,070,904). We estimated sex- and age-specific incidence rates of nine adverse outcomes, in three main categories: Premature mortality (all-causes, suicide, accident); Psychiatric morbidity (any mental illness diagnosis, suicide attempt, alcohol or drug misuse disorder); Criminality (violent offending, receiving custodial sentence, driving under influence of alcohol or drugs). Cumulative incidences were also calculated using competing risk survival analyses. RESULTS: For cohort members alive on their 15(th) birthday, the absolute risks of dying by age 40 were 1.99 % for males [95 % confidence interval (CI) 1.95–2.03 %] and 0.85 % for females (95 % CI 0.83–0.88 %). The risks of substance misuse and criminality were also much higher for males, especially younger males, than for females. Specifically, the risk of a first conviction for a violent offence was highest amongst males aged below 20. Females, however, were more likely than males to have a hospital-treated psychiatric disorder. By age 40, 13.25 % of females (95 % CI 13.16–13.33 %) and 9.98 % of males (95 % CI 9.91–10.06 %) had been treated. Women aged below 25 were also more likely than men to first attempt suicide, but this pattern was reversed beyond this age. The greatest gender differentials in incidence rates were in criminality outcomes. CONCLUSIONS: This is the first comprehensive assessment of the incidence rates and absolute risks of these multiple adverse outcomes. Approximately 1 in 50 males and 1 in 120 females who are alive on their 15th birthday will die by age 40. By examining the same cohort at risk, we compared risks for multiple outcomes without differential inter-cohort biases. These epidemiological profiles will inform further research into the pathways leading to these adverse events and future preventive strategies.
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spelling pubmed-45754322015-09-20 National cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age Mok, Pearl L.H. Antonsen, Sussie Pedersen, Carsten Bøcker Appleby, Louis Shaw, Jenny Webb, Roger T. BMC Public Health Research Article BACKGROUND: Psychiatric illness, substance misuse, suicidality, criminality and premature death represent major public health challenges that afflict a sizeable proportion of young people. However, studies of multiple adverse outcomes in the same cohort at risk are rare. In a national Danish cohort we estimated sex- and age-specific incidence rates and absolute risks of these outcomes between adolescence and early middle age. METHODS: Using interlinked registers, persons born in Denmark 1966–1996 were followed from their 15(th) until 40(th) birthday or December 2011 (N = 2,070,904). We estimated sex- and age-specific incidence rates of nine adverse outcomes, in three main categories: Premature mortality (all-causes, suicide, accident); Psychiatric morbidity (any mental illness diagnosis, suicide attempt, alcohol or drug misuse disorder); Criminality (violent offending, receiving custodial sentence, driving under influence of alcohol or drugs). Cumulative incidences were also calculated using competing risk survival analyses. RESULTS: For cohort members alive on their 15(th) birthday, the absolute risks of dying by age 40 were 1.99 % for males [95 % confidence interval (CI) 1.95–2.03 %] and 0.85 % for females (95 % CI 0.83–0.88 %). The risks of substance misuse and criminality were also much higher for males, especially younger males, than for females. Specifically, the risk of a first conviction for a violent offence was highest amongst males aged below 20. Females, however, were more likely than males to have a hospital-treated psychiatric disorder. By age 40, 13.25 % of females (95 % CI 13.16–13.33 %) and 9.98 % of males (95 % CI 9.91–10.06 %) had been treated. Women aged below 25 were also more likely than men to first attempt suicide, but this pattern was reversed beyond this age. The greatest gender differentials in incidence rates were in criminality outcomes. CONCLUSIONS: This is the first comprehensive assessment of the incidence rates and absolute risks of these multiple adverse outcomes. Approximately 1 in 50 males and 1 in 120 females who are alive on their 15th birthday will die by age 40. By examining the same cohort at risk, we compared risks for multiple outcomes without differential inter-cohort biases. These epidemiological profiles will inform further research into the pathways leading to these adverse events and future preventive strategies. BioMed Central 2015-09-19 /pmc/articles/PMC4575432/ /pubmed/26386672 http://dx.doi.org/10.1186/s12889-015-2249-5 Text en © Mok et al. 2015 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
Mok, Pearl L.H.
Antonsen, Sussie
Pedersen, Carsten Bøcker
Appleby, Louis
Shaw, Jenny
Webb, Roger T.
National cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age
title National cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age
title_full National cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age
title_fullStr National cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age
title_full_unstemmed National cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age
title_short National cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age
title_sort national cohort study of absolute risk and age-specific incidence of multiple adverse outcomes between adolescence and early middle age
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575432/
https://www.ncbi.nlm.nih.gov/pubmed/26386672
http://dx.doi.org/10.1186/s12889-015-2249-5
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