AI Article Synopsis

  • The burden of dementia is increasing worldwide, and more accurate predictions of its prevalence are needed for planning an aging population.
  • The Dementia Population Risk Tool (DemPoRT) will use advanced statistical methods on data from the Canadian Community Health Survey to project dementia incidence and identify risk factors among elderly respondents in Ontario.
  • Ethics approval has been obtained for the study, and findings will be published and accessible online for public and individual use.

Article Abstract

Introduction: The burden of disease from dementia is a growing global concern as incidence increases dramatically with age, and average life expectancy has been increasing around the world. Planning for an ageing population requires reliable projections of dementia prevalence; however, existing population projections are simple and have poor predictive accuracy. The Dementia Population Risk Tool (DemPoRT) will predict incidence of dementia in the population setting using multivariable modelling techniques and will be used to project dementia prevalence.

Methods And Analysis: The derivation cohort will consist of elderly Ontario respondents of the Canadian Community Health Survey (CCHS) (2001, 2003, 2005 and 2007; 18 764 males and 25 288 females). Prespecified predictors include sociodemographic, general health, behavioural, functional and health condition variables. Incident dementia will be identified through individual linkage of survey respondents to population-level administrative healthcare databases (1797 and 3281 events, and 117 795 and 166 573 person-years of follow-up, for males and females, respectively, until 31 March 2014). Using time of first dementia capture as the primary outcome and death as a competing risk, sex-specific proportional hazards regression models will be estimated. The 2008/2009 CCHS survey will be used for validation (approximately 4600 males and 6300 females). Overall calibration and discrimination will be assessed as well as calibration within predefined subgroups of importance to clinicians and policy makers.

Ethics And Dissemination: Research ethics approval has been granted by the Ottawa Health Science Network Research Ethics Board. DemPoRT results will be submitted for publication in peer-review journals and presented at scientific meetings. The algorithm will be assessable online for both population and individual uses.

Trial Registration Number: ClinicalTrials.gov NCT03155815, pre-results.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665213PMC
http://dx.doi.org/10.1136/bmjopen-2017-018018DOI Listing

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