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Work-family life courses and metabolic markers in mid-life: evidence from the British National Child Development Study

BACKGROUND: Previous studies have found generally better health among those who combine employment and family responsibilities; however, most research excludes men, and relies on subjective measures of health and information on work and family activities from only 1 or 2 time points in the life cour...

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Autores principales: McMunn, Anne, Lacey, Rebecca E, Kumari, Meena, Worts, Diana, McDonough, Peggy, Sacker, Amanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853544/
https://www.ncbi.nlm.nih.gov/pubmed/26659761
http://dx.doi.org/10.1136/jech-2015-206036
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author McMunn, Anne
Lacey, Rebecca E
Kumari, Meena
Worts, Diana
McDonough, Peggy
Sacker, Amanda
author_facet McMunn, Anne
Lacey, Rebecca E
Kumari, Meena
Worts, Diana
McDonough, Peggy
Sacker, Amanda
author_sort McMunn, Anne
collection PubMed
description BACKGROUND: Previous studies have found generally better health among those who combine employment and family responsibilities; however, most research excludes men, and relies on subjective measures of health and information on work and family activities from only 1 or 2 time points in the life course. This study investigated associations between work-family life course types (LCTs) and markers of metabolic risk in a British birth cohort study. METHODS: Multichannel sequence analysis was used to generate work-family LCTs, combining annual information on work, partnership and parenthood between 16 and 42 years for men and women in the British National Child Development Study (NCDS, followed since their birth in 1958). Associations between work-family LCTs and metabolic risk factors in mid-life (age 44–45) were tested using multivariate linear regression in multiply imputed data. RESULTS: Life courses characterised by earlier transitions into parenthood were associated with significantly increased metabolic risk, regardless of attachment to paid work or marital stability over the life course. These associations were only partially attenuated by educational qualifications, early life circumstances and adult mediators. The positive association between weak labour markets ties and metabolic risk was weaker than might be expected from previous studies. Associations between work-family LCTs and metabolic risk factors did not differ significantly by gender. CONCLUSIONS: Earlier transitions to parenthood are linked to metabolic risk in mid-life.
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spelling pubmed-48535442016-05-06 Work-family life courses and metabolic markers in mid-life: evidence from the British National Child Development Study McMunn, Anne Lacey, Rebecca E Kumari, Meena Worts, Diana McDonough, Peggy Sacker, Amanda J Epidemiol Community Health Research Report BACKGROUND: Previous studies have found generally better health among those who combine employment and family responsibilities; however, most research excludes men, and relies on subjective measures of health and information on work and family activities from only 1 or 2 time points in the life course. This study investigated associations between work-family life course types (LCTs) and markers of metabolic risk in a British birth cohort study. METHODS: Multichannel sequence analysis was used to generate work-family LCTs, combining annual information on work, partnership and parenthood between 16 and 42 years for men and women in the British National Child Development Study (NCDS, followed since their birth in 1958). Associations between work-family LCTs and metabolic risk factors in mid-life (age 44–45) were tested using multivariate linear regression in multiply imputed data. RESULTS: Life courses characterised by earlier transitions into parenthood were associated with significantly increased metabolic risk, regardless of attachment to paid work or marital stability over the life course. These associations were only partially attenuated by educational qualifications, early life circumstances and adult mediators. The positive association between weak labour markets ties and metabolic risk was weaker than might be expected from previous studies. Associations between work-family LCTs and metabolic risk factors did not differ significantly by gender. CONCLUSIONS: Earlier transitions to parenthood are linked to metabolic risk in mid-life. BMJ Publishing Group 2016-05 2015-12-12 /pmc/articles/PMC4853544/ /pubmed/26659761 http://dx.doi.org/10.1136/jech-2015-206036 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Research Report
McMunn, Anne
Lacey, Rebecca E
Kumari, Meena
Worts, Diana
McDonough, Peggy
Sacker, Amanda
Work-family life courses and metabolic markers in mid-life: evidence from the British National Child Development Study
title Work-family life courses and metabolic markers in mid-life: evidence from the British National Child Development Study
title_full Work-family life courses and metabolic markers in mid-life: evidence from the British National Child Development Study
title_fullStr Work-family life courses and metabolic markers in mid-life: evidence from the British National Child Development Study
title_full_unstemmed Work-family life courses and metabolic markers in mid-life: evidence from the British National Child Development Study
title_short Work-family life courses and metabolic markers in mid-life: evidence from the British National Child Development Study
title_sort work-family life courses and metabolic markers in mid-life: evidence from the british national child development study
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853544/
https://www.ncbi.nlm.nih.gov/pubmed/26659761
http://dx.doi.org/10.1136/jech-2015-206036
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