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A statistical model to describe longitudinal and correlated metabolic risk factors: the Whitehall II prospective study

BACKGROUND: Novel epidemiology models are required to link correlated variables over time, especially haemoglobin A1c (HbA1c) and body mass index (BMI) for diabetes prevention policy analysis. This article develops an epidemiology model to correlate metabolic risk factor trajectories. METHOD: BMI, f...

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Autores principales: Breeze, P., Squires, H., Chilcott, J., Stride, C., Diggle, P.J., Brunner, E., Tabak, A., Brennan, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092879/
https://www.ncbi.nlm.nih.gov/pubmed/28158533
http://dx.doi.org/10.1093/pubmed/fdv160
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author Breeze, P.
Squires, H.
Chilcott, J.
Stride, C.
Diggle, P.J.
Brunner, E.
Tabak, A.
Brennan, A.
author_facet Breeze, P.
Squires, H.
Chilcott, J.
Stride, C.
Diggle, P.J.
Brunner, E.
Tabak, A.
Brennan, A.
author_sort Breeze, P.
collection PubMed
description BACKGROUND: Novel epidemiology models are required to link correlated variables over time, especially haemoglobin A1c (HbA1c) and body mass index (BMI) for diabetes prevention policy analysis. This article develops an epidemiology model to correlate metabolic risk factor trajectories. METHOD: BMI, fasting plasma glucose, 2-h glucose, HbA1c, systolic blood pressure, total cholesterol and high density lipoprotein (HDL) cholesterol were analysed over 16 years from 8150 participants of the Whitehall II prospective cohort study. Latent growth curve modelling was employed to simultaneously estimate trajectories for multiple metabolic risk factors allowing for variation between individuals. A simulation model compared simulated outcomes with the observed data. RESULTS: The model identified that the change in BMI was associated with changes in glycaemia, total cholesterol and systolic blood pressure. The statistical analysis quantified associations among the longitudinal risk factor trajectories. Growth in latent glycaemia was positively correlated with systolic blood pressure and negatively correlated with HDL cholesterol. The goodness-of-fit analysis indicates reasonable fit to the data. CONCLUSIONS: This is the first statistical model that estimates trajectories of metabolic risk factors simultaneously for diabetes to predict joint correlated risk factor trajectories. This can inform comparisons of the effectiveness and cost-effectiveness of preventive interventions, which aim to modify metabolic risk factors.
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spelling pubmed-60928792018-08-22 A statistical model to describe longitudinal and correlated metabolic risk factors: the Whitehall II prospective study Breeze, P. Squires, H. Chilcott, J. Stride, C. Diggle, P.J. Brunner, E. Tabak, A. Brennan, A. J Public Health (Oxf) Original Article BACKGROUND: Novel epidemiology models are required to link correlated variables over time, especially haemoglobin A1c (HbA1c) and body mass index (BMI) for diabetes prevention policy analysis. This article develops an epidemiology model to correlate metabolic risk factor trajectories. METHOD: BMI, fasting plasma glucose, 2-h glucose, HbA1c, systolic blood pressure, total cholesterol and high density lipoprotein (HDL) cholesterol were analysed over 16 years from 8150 participants of the Whitehall II prospective cohort study. Latent growth curve modelling was employed to simultaneously estimate trajectories for multiple metabolic risk factors allowing for variation between individuals. A simulation model compared simulated outcomes with the observed data. RESULTS: The model identified that the change in BMI was associated with changes in glycaemia, total cholesterol and systolic blood pressure. The statistical analysis quantified associations among the longitudinal risk factor trajectories. Growth in latent glycaemia was positively correlated with systolic blood pressure and negatively correlated with HDL cholesterol. The goodness-of-fit analysis indicates reasonable fit to the data. CONCLUSIONS: This is the first statistical model that estimates trajectories of metabolic risk factors simultaneously for diabetes to predict joint correlated risk factor trajectories. This can inform comparisons of the effectiveness and cost-effectiveness of preventive interventions, which aim to modify metabolic risk factors. Oxford University Press 2016-12 2015-11-06 /pmc/articles/PMC6092879/ /pubmed/28158533 http://dx.doi.org/10.1093/pubmed/fdv160 Text en © The Author 2015. Published by Oxford University Press on behalf of Faculty of Public Health. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Breeze, P.
Squires, H.
Chilcott, J.
Stride, C.
Diggle, P.J.
Brunner, E.
Tabak, A.
Brennan, A.
A statistical model to describe longitudinal and correlated metabolic risk factors: the Whitehall II prospective study
title A statistical model to describe longitudinal and correlated metabolic risk factors: the Whitehall II prospective study
title_full A statistical model to describe longitudinal and correlated metabolic risk factors: the Whitehall II prospective study
title_fullStr A statistical model to describe longitudinal and correlated metabolic risk factors: the Whitehall II prospective study
title_full_unstemmed A statistical model to describe longitudinal and correlated metabolic risk factors: the Whitehall II prospective study
title_short A statistical model to describe longitudinal and correlated metabolic risk factors: the Whitehall II prospective study
title_sort statistical model to describe longitudinal and correlated metabolic risk factors: the whitehall ii prospective study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092879/
https://www.ncbi.nlm.nih.gov/pubmed/28158533
http://dx.doi.org/10.1093/pubmed/fdv160
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