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Intelligence and Disability Pension in Swedish Men and Women Followed from Childhood to Late Middle Age

OBJECTIVE: To investigate the association between intelligence and disability pension due to mental, musculoskeletal, cardiovascular, and substance-use disorders among men and women, and to assess the role of childhood social factors and adulthood work characteristics. METHODS: Two random samples of...

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Autores principales: Lundin, Andreas, Sörberg Wallin, Alma, Falkstedt, Daniel, Allebeck, Peter, Hemmingsson, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465631/
https://www.ncbi.nlm.nih.gov/pubmed/26062026
http://dx.doi.org/10.1371/journal.pone.0128834
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author Lundin, Andreas
Sörberg Wallin, Alma
Falkstedt, Daniel
Allebeck, Peter
Hemmingsson, Tomas
author_facet Lundin, Andreas
Sörberg Wallin, Alma
Falkstedt, Daniel
Allebeck, Peter
Hemmingsson, Tomas
author_sort Lundin, Andreas
collection PubMed
description OBJECTIVE: To investigate the association between intelligence and disability pension due to mental, musculoskeletal, cardiovascular, and substance-use disorders among men and women, and to assess the role of childhood social factors and adulthood work characteristics. METHODS: Two random samples of men and women born 1948 and 1953 (n = 10 563 and 9 434), and tested for general intelligence at age 13, were followed in registers for disability pension until 2009. Physical and psychological strains in adulthood were assessed using job exposure matrices. Associations were examined using Cox proportional hazard regression models, with increases in rates reported as hazard ratios (HRs) with 95% confidence intervals (95%CI) per decrease in stanine intelligence. RESULTS: In both men and women increased risks were found for disability pension due to all causes, musculoskeletal disorder, mental disorder other than substance use, and cardiovascular disease as intelligence decreased. Increased risk was also found for substance use disorder in men. In multivariate models, HRs were attenuated after controlling for pre-school plans in adolescence, and low job control and high physical strain in adulthood. In the fully adjusted model, increased HRs remained for all causes (male HR 1.11, 95%CI 1.07–1.15, female HR 1.06, 95%CI 1.02–1.09) and musculoskeletal disorder (male HR 1.16, 95%CI 1.09–1.24, female HR 1.08, 95%CI 1.03–1.14) during 1986 to 2009. CONCLUSION: Relatively low childhood intelligence is associated with increased risk of disability pension due to musculoskeletal disorder in both men and women, even after adjustment for risk factors for disability pension measured over the life course.
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spelling pubmed-44656312015-06-25 Intelligence and Disability Pension in Swedish Men and Women Followed from Childhood to Late Middle Age Lundin, Andreas Sörberg Wallin, Alma Falkstedt, Daniel Allebeck, Peter Hemmingsson, Tomas PLoS One Research Article OBJECTIVE: To investigate the association between intelligence and disability pension due to mental, musculoskeletal, cardiovascular, and substance-use disorders among men and women, and to assess the role of childhood social factors and adulthood work characteristics. METHODS: Two random samples of men and women born 1948 and 1953 (n = 10 563 and 9 434), and tested for general intelligence at age 13, were followed in registers for disability pension until 2009. Physical and psychological strains in adulthood were assessed using job exposure matrices. Associations were examined using Cox proportional hazard regression models, with increases in rates reported as hazard ratios (HRs) with 95% confidence intervals (95%CI) per decrease in stanine intelligence. RESULTS: In both men and women increased risks were found for disability pension due to all causes, musculoskeletal disorder, mental disorder other than substance use, and cardiovascular disease as intelligence decreased. Increased risk was also found for substance use disorder in men. In multivariate models, HRs were attenuated after controlling for pre-school plans in adolescence, and low job control and high physical strain in adulthood. In the fully adjusted model, increased HRs remained for all causes (male HR 1.11, 95%CI 1.07–1.15, female HR 1.06, 95%CI 1.02–1.09) and musculoskeletal disorder (male HR 1.16, 95%CI 1.09–1.24, female HR 1.08, 95%CI 1.03–1.14) during 1986 to 2009. CONCLUSION: Relatively low childhood intelligence is associated with increased risk of disability pension due to musculoskeletal disorder in both men and women, even after adjustment for risk factors for disability pension measured over the life course. Public Library of Science 2015-06-10 /pmc/articles/PMC4465631/ /pubmed/26062026 http://dx.doi.org/10.1371/journal.pone.0128834 Text en © 2015 Lundin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lundin, Andreas
Sörberg Wallin, Alma
Falkstedt, Daniel
Allebeck, Peter
Hemmingsson, Tomas
Intelligence and Disability Pension in Swedish Men and Women Followed from Childhood to Late Middle Age
title Intelligence and Disability Pension in Swedish Men and Women Followed from Childhood to Late Middle Age
title_full Intelligence and Disability Pension in Swedish Men and Women Followed from Childhood to Late Middle Age
title_fullStr Intelligence and Disability Pension in Swedish Men and Women Followed from Childhood to Late Middle Age
title_full_unstemmed Intelligence and Disability Pension in Swedish Men and Women Followed from Childhood to Late Middle Age
title_short Intelligence and Disability Pension in Swedish Men and Women Followed from Childhood to Late Middle Age
title_sort intelligence and disability pension in swedish men and women followed from childhood to late middle age
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465631/
https://www.ncbi.nlm.nih.gov/pubmed/26062026
http://dx.doi.org/10.1371/journal.pone.0128834
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