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A population-based risk algorithm for the development of diabetes: development and validation of the Diabetes Population Risk Tool (DPoRT)

BACKGROUND: National estimates of the upcoming diabetes epidemic are needed to understand the distribution of diabetes risk in the population and to inform health policy. OBJECTIVE: To create and validate a population-based risk prediction tool for incident diabetes using commonly collected national...

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Autores principales: Rosella, Laura C, Manuel, Douglas G, Burchill, Charles, Stukel, Thérèse A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112365/
https://www.ncbi.nlm.nih.gov/pubmed/20515896
http://dx.doi.org/10.1136/jech.2009.102244
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author Rosella, Laura C
Manuel, Douglas G
Burchill, Charles
Stukel, Thérèse A
author_facet Rosella, Laura C
Manuel, Douglas G
Burchill, Charles
Stukel, Thérèse A
author_sort Rosella, Laura C
collection PubMed
description BACKGROUND: National estimates of the upcoming diabetes epidemic are needed to understand the distribution of diabetes risk in the population and to inform health policy. OBJECTIVE: To create and validate a population-based risk prediction tool for incident diabetes using commonly collected national survey data. METHODS: With the use of a cohort design that links baseline risk factors to a validated population-based diabetes registry, a model (Diabetes Population Risk Tool (DPoRT)) was developed to predict 9-year risk for diabetes. The probability of developing diabetes was modelled using sex-specific Weibull survival functions for people >20 years of age without diabetes (N=19 861). The model was validated in two external cohorts in Ontario (N=26 465) and Manitoba (N=9899). Predictive accuracy and model performance were assessed by comparing observed diabetes rates with predicted estimates. Discrimination and calibration were measured using a C statistic and Hosmer–Lemeshow χ(2) statistic (χ2(H–L)). RESULTS: Predictive factors included were body mass index, age, ethnicity, hypertension, immigrant status, smoking, education status and heart disease. DPoRT showed good discrimination (C=0.77–0.80) and calibration (χ(2)(H–L) <20) in both external validation cohorts. CONCLUSIONS: This algorithm can be used to estimate diabetes incidence and quantify the effect of interventions using routinely collected survey data.
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spelling pubmed-31123652011-06-27 A population-based risk algorithm for the development of diabetes: development and validation of the Diabetes Population Risk Tool (DPoRT) Rosella, Laura C Manuel, Douglas G Burchill, Charles Stukel, Thérèse A J Epidemiol Community Health Research Report BACKGROUND: National estimates of the upcoming diabetes epidemic are needed to understand the distribution of diabetes risk in the population and to inform health policy. OBJECTIVE: To create and validate a population-based risk prediction tool for incident diabetes using commonly collected national survey data. METHODS: With the use of a cohort design that links baseline risk factors to a validated population-based diabetes registry, a model (Diabetes Population Risk Tool (DPoRT)) was developed to predict 9-year risk for diabetes. The probability of developing diabetes was modelled using sex-specific Weibull survival functions for people >20 years of age without diabetes (N=19 861). The model was validated in two external cohorts in Ontario (N=26 465) and Manitoba (N=9899). Predictive accuracy and model performance were assessed by comparing observed diabetes rates with predicted estimates. Discrimination and calibration were measured using a C statistic and Hosmer–Lemeshow χ(2) statistic (χ2(H–L)). RESULTS: Predictive factors included were body mass index, age, ethnicity, hypertension, immigrant status, smoking, education status and heart disease. DPoRT showed good discrimination (C=0.77–0.80) and calibration (χ(2)(H–L) <20) in both external validation cohorts. CONCLUSIONS: This algorithm can be used to estimate diabetes incidence and quantify the effect of interventions using routinely collected survey data. BMJ Group 2010-06-01 2011-07 /pmc/articles/PMC3112365/ /pubmed/20515896 http://dx.doi.org/10.1136/jech.2009.102244 Text en © 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Research Report
Rosella, Laura C
Manuel, Douglas G
Burchill, Charles
Stukel, Thérèse A
A population-based risk algorithm for the development of diabetes: development and validation of the Diabetes Population Risk Tool (DPoRT)
title A population-based risk algorithm for the development of diabetes: development and validation of the Diabetes Population Risk Tool (DPoRT)
title_full A population-based risk algorithm for the development of diabetes: development and validation of the Diabetes Population Risk Tool (DPoRT)
title_fullStr A population-based risk algorithm for the development of diabetes: development and validation of the Diabetes Population Risk Tool (DPoRT)
title_full_unstemmed A population-based risk algorithm for the development of diabetes: development and validation of the Diabetes Population Risk Tool (DPoRT)
title_short A population-based risk algorithm for the development of diabetes: development and validation of the Diabetes Population Risk Tool (DPoRT)
title_sort population-based risk algorithm for the development of diabetes: development and validation of the diabetes population risk tool (dport)
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112365/
https://www.ncbi.nlm.nih.gov/pubmed/20515896
http://dx.doi.org/10.1136/jech.2009.102244
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